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Annarbor - Associate Scientist -- MWH Global

MWH is an employee owned company and a global leader in engineering, environmental, construction, technology, and management services. With more than $1 billion in revenue, our 6,100 professionals located in 190 offices in 36 countries provide premiere solutions and expertise to municipalities, government agencies, industries, multinational corporations, and military organizations worldwide. Job Description: MWH's Metro Detroit-area office of the Natural Resources Industry and Infrastructure division is seeking a technical professional interested in working with a local team networked with other MWH staff around the world to serve multi-national, industrial clients.Position requires significant travel (sometimes internationally) to execute all types of field activities associated with environmental (soil/groundwater) investigations, environmental/health/safety audits, and Phase I ESA due diligence projects for business acquisitions/divestitures.Assistance with report preparation also required; therefore, strong computers skills are a plus.Work loads are dynamic and unpredictable.Individual must be very flexible, willing to travel, and enjoy projects that are very diverse. Experience Required: Minimum BS degree in science or engineering; degrees in geology, geotechnical engineering, hydrogeology, or environmental engineering are very desirable.1-2 years experience in the environmental industry a plus, but not required if person has some field experience from college.Strong computer, writing, and verbal skills are required. Keywords: Associate Scientist APPLY ONLINE Employer Job Code: mw-00005097 [GJ.4235141.19]

Annarbor - * Get paid what your worth!!! *2982984

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Annarbor - Regional Clinical Research Associate, 70-90k

Please email your resume if you are interested in being contacted for an interview. Requirements: A minimum of 2 years experience as a regional CRA, more is better. 4 year degree 60 % travel 70-90K, outstanding benefits Thank-you for your time and interest!

Annarbor - Immunology Scientist/Head of Research

Funded biotech startup that develops monoclonal antibody therapies for organ transplantation and oncology has an opportunity for a head of research in concert with the founding scientist—and would be joining an executive team experienced in startups. Interested parties can contact Amy Cell, Amy@AnnArborSPARK.org.

Annarbor - Regulatory Affairs and Quality Director

Tissue Regeneration Systems, Inc. (TRS) is an exciting venture-backed University of Michigan start-up developing breakthrough bioactive spine, CMF, and orthopedic implants. We are now seeking bright, highly motivated individuals to become key members of our team. Primary responsibility is to lead all facets of the company’s regulatory activities. This includes: · Participate on product development teams to insure US and EU regulatory requirements are incorporated as part of the development process · Address and advise teams on appropriate regulatory pathways to market, working with FDA Guidance Documents and outside consultants as needed · Author submissions and other regulatory documents to obtain approval to bring new or modified products to market including but not limited to 510(k)'s, IDE's, PMA's, Technical Files, and Design Dossiers · Interface and coordinate with the FDA, Notified Bodies, Competent Authorities and other regulatory agencies on submissions, approvals or other issues · Establish and maintain regulatory information systems, design history files, both electronically and hard copy · Develop, implement and maintain regulatory SOP's Conduct quality and regulatory training · Secondary responsibility is to set up and manage cGMP systems. REQUIREMENTS Experience with spine, orthopedics, and biodegradable devices strongly desired 510(k) and IDE (original/revision/supplements) preparation experience Preparation of EU Technical Files and Design Dossiers desirable Minimum 5 years experience in FDA and EU regulated medical device industry Working knowledge of FDA and EU Medical Device Regulations Direct interaction with FDA reviewers/inspectors B.S. or B.A. degree minimum Interested parties should send resume to Amy@AnnArborSPARK.org

Annarbor - Lead Biomaterials Engineer

Tissue Regeneration Systems, Inc. (TRS) is an exciting venture-backed University of Michigan start-up developing breakthrough bioactive spine, CMF, and orthopedic implants. We are now seeking bright, highly motivated individuals to become key members of our team. JOB DESCRIPTION Primary responsibility is leading all development and analysis of biologically active medical device coatings Perform surface characterization, including chemical assays, SEM, FTIR, and XRD analysis Perform biological characterization, including biochemical assays and cell culture REQUIREMENTS Prior work with biodegradable polymers and calcium phosphate minerals beneficial Medical device development experience (spine/orthopedics or related experience strongly desired) Experience with drug delivery beneficial B.S. Biomedical Engineering, Materials Science, Chemical Engineering or Chemistry, with an emphasis in biomaterials or tissue engineering, plus a minimum of 5 years experience, or M.S. or Ph.D. in above areas and a minimum of 3 years experience Interested parties should send resume to Amy@AnnArborSPARK.org

Annarbor - Product Development Manager

This position is responsible for developing new products within identified schedule, personnel and budget constraints. Supervise and develop subordinates. 1. Maintain and follow proper compliance and quality systems requirements. 2. Lead and manage cross-functional product development teams in the design and development of cardiovascular surgery products. 3. Plan and formulate aspects of new project proposals. 4. Develop and assess new technologies and product ideas for profitability, fit, feasibility, safety and effectiveness. 5. Work closely with other engineering managers and project leaders to drive projects to completion within identified schedule and budget constraints. 6. Provide engineering support to the manufacturing, quality and marketing departments. 7. Carry out supervisory responsibilities in accordance with the organization's policies. 8. Create and revise procedures to assure compliance with the ISO directive and medical device regulations. Requires a four-year college degree in Engineering or Sciences coupled with 5-10 years experience in product development, at least 3 years at engineering supervisor level. Minimum 3 years experience in Catheter/Cannula design and development. Demonstrated high degree of creativity, foresight, and sound judgment in planning, organizing, and leading engineering projects and activities. Background in 510(k) required. Knowledge of PMAs helpful. Familiar with GMP and ISO compliance. Exposure to QA, RA and manufacturing. Solid track record of successful product introductions from concept to manufacturing. Excellent communication and people skills.

Annarbor - Associate Toxicologist I

We are looking for an Associate Toxicologist I for our Toxicology Services group, to compile, review, interpret, and process chemical and toxicological information submitted in support of applications for certification and/or registration.PRINCIPAL ACCOUNTABILITIES:Review the chemical composition of materials to determine appropriate chemical extraction testing.Collaborating with chemistry, exposure and physical lab personnel prior to testing, inspecting samples, and reviewing the extraction process when deemed necessary, to ensure proper product evaluation.Support other business units as a toxicology consultant in relation to regulatory compliance, product safety, risk assessment, and risk management.Represent the company at technical meetings and trade shows.Communicate with customers on technical issues relating to product compliance.Develop chemical action levels by reviewing, summarizing and interpreting toxicology studies to assess potential human health risks.Interact with internal and external customer representatives to resolve issues related to product compliance.Author and revise standard operating procedures.Attend and actively participate in industry forums.Understand and apply the requirements of various standards for products submitted for certification.Perform other duties as requested.REQUIRED QUALIFICATIONS:Bachelor’s degree in toxicology or related science. One year related work experienceKnowledge of basic chemistry.Familiarity with toxicology studies and risk assessment.Ability to perform multiple tasks and meet deadlines in a goal-oriented atmosphereAbility to work independently with minimal supervisionEffective written, oral, and presentation skills.Strong interpersonal skills.Attention to detail.PREFERRED QUALIFICAITONS:Bachelor’s degree in toxicology with two or more years related work experience.Experience in conducting and/or evaluating toxicology studies.Experience with computer-based statistical analyses. No phone calls, faxes or postal mail please. *Smoke free work environment* NSF and its subsidiaries are EO/AA employers - we welcome and encourage diversity in our workplace Please apply at: NSF Careers

Annarbor - BIOSTATISTICIAN

I am working on a project for an extremely large pharmaceutical company, who is currently looking for several Clinical and Non-Clinical Biostatisticians at various levels at multiple locations. If you are a Clinical or Non-Clinical Biostatistician who is looking for a position within a large pharmaceutical company please send me your CV. Alternatively, if you may know of someone who might be a good fit for this role, I would also welcome the opportunity of contacting them. I have attached both Job Descriptions for your interest and I look forward to hearing from you regarding your thoughts. Thank you for your time. Regards, Ed Swiacki Augustine Inc. JOB DESCRIPTION Posting Title:Non-Clinical Biostatistician (Manager/Associate Director) Job Requisition:058275 Posting Locations CountryStateCity USACTGroton, St. Louis. Missouri,and La Jolla, California Responsibilities:Visible: Internal and External BRIEF DESCRIPTION OF DUTIES AND RESPONSIBILITIES: The Research Statistics group provides support to a wide variety of nonclinical activities in drug discovery, pharmaceutical development and manufacturing. Key roles: - Provide statistical support to nonclinical areas of R&D, including: Discovery, Drug Safety R&D, and PDM (Pharmacokinetics, Dynamics, and Metabolism) organizations. - Collaborate with scientists to plan meaningful experimental studies, statistically analyze study data, and communicate results. - Work with programmers to create tools that facilitate use of advanced statistical methodology by Pfizer scientists. Specific projects involve, for example: - In vivo - in vitro bioassay development / validation as markers of preclinical and clinical drug activity and safety. - Genomic studies to support drug target confidence and biomarker discovery. - Developing computational models to predict properties of chemical compounds. - Participation on cross-functional full development nonclinical drug project teams to recommend appropriate statistical applications and plan / execute recommendations. - Perform statistical analyses of study results, write summary reports and present orally. - Monitor literature for new statistical methodology and apply or adapt as appropriate. - Increase knowledge relating to the pharmaceutical regulatory environment and / or appropriate pharmaceutical application area. - Develop and deliver statistical training modules to meet the needs of Pfizer scientific lines. Qualifications:Visible: Internal and External QUALIFICATIONS SOUGHT: 1.EDUCATIONAL BACKGROUND: MINIMUM: M.S. Statistics or Biostatistics DESIRABLE: Ph.D. Statistics or Biostatistics 2.WORK EXPERIENCE/SKILLS: Requirements: A minimum of an M.S. in Statistics is required; a Ph.D. in Statistics is desired. Two years statistical consulting experience, preferably in a laboratory science environment as well as a strong science background, with good working knowledge of biology, chemistry, engineering, or pharmacology is required. Good computational skills in SAS, S-plus or R. Good written and verbal communication skills. Clinical Biostatistician Posting Title:Manager/Associate Director/Director/Sr Director Statistics Location CountryStateCity USANew London, Connecticut; San Diego, California; New York City, New York Responsibilities: Provide statistical support for drug development projects in the cardiovascular/metabolic/endocrine therapeutic area. Accountable for the design and analysis of clinical trials and for components of development plans and regulatory filings. Participate on project teams and be a liaison between the statistics line and other discipline lines for that project. Participate in and support regulatory meetings. May also oversee activities of other statisticians. Qualifications: EDUCATIONAL BACKGROUND Minimum: MS in Statistics or Biostatistics plus 3-15 years of experience in pharmaceutical drug development. Desirable: PhD in Statistics, Biostatistics or related field plus 1-5 years of experience in pharmaceutical drug development. WORK EXPERIENCE/SKILLS Minimum: Programming experience in statistical applications. Strong communication and teamwork skills. Ability to work effectively and independently. Desirable: Experience with drug development and preferably in the cardiovascular/metabolic/endocrine area. Participation on drug development teams. Participation in development planning. Other Attributes Desirable: Participation in regulatory interactions (e.g. FDA). Participation in regulatory filings. Mentoring or supervisory experience. Equal Employment Opportunity:

Annarbor - Associate Technician - Multiple temp to hire entry level lab positions

NSF International, an independent, not-for-profit organization, helps protect you by certifying products and writing standards for food, water, air and consumer goods (www.nsf.org). Founded in 1944, NSF is committed to protecting public health and safety worldwide. Additional services include safety audits for the food and water industries, management systems registrations delivered through NSF International Strategic Registrations, Ltd., organic certification provided by Quality Assurance International and education through the NSF Center for Public Health Education. We have multiple openings in our Chemistry Lab for temporary associate technicians to assist with basic laboratory procedures and train to increase laboratory skills. Some openings may lead to a direct hire opportunity.. Required Qualifications:Two (2) years of completed college level coursework in a physical science along with six (6) months of relevant laboratory and/or testing experience.Experience with wet and instrumental techniques.Good written and verbal communication skills.Experience with PCs and Windows applications.Excellent attention to detail.Some weekend work is necessaryPhysical Demand:Up to 90% standing, walking between areas within the laboratory and building.Ability to lift approximately 60 pounds. Work with various chemicals, solvents, acids, and bases with MSDS use.Reaching and handling samples within hot and room temperature settings.Visual skills required to notice certain aspects of samples and dirty exposure vessels. No phone calls, faxes or postal mail please. *Smoke free work environment* NSF and its subsidiaries are EO/AA employers - we welcome and encourage diversity in our workplace Please apply at: NSF Careers

Annarbor - Data Analyst (Research Health Science Specialist)

Job Description: Assist with data analysis and data management for health services research projects at a national research center in the Veterans Affairs health system. Qualifications: * Able to program, manage data, and conduct statistical analyses using SAS. * Has demonstrated data management skills and experience preparing data for analysis. * Has a solid grounding in statistical theory and application, and willingness to learn and apply new methods and approaches. * Able to work independently and as part of research team. * Proficient at data analysis using: multiple regression; analysis of variance; bivariate and univariate descriptive techniques; and must be familiar with the statistical assumptions underlying these methods. Experience and training with survival analysis, multilevel modeling, and large data sets a plus. * Familiar with other statistical/programming software, e.g., SPSS, STATA, SQL. * Proficient at summarizing statistical methods and results in writing with the quality necessary for manuscript preparation. * Experienced preparing graphs, figures, and illustrations of the results of statistical analyses. * Competent with Excel and able to import data from Excel into SAS. * Experience/training in the health and social sciences a plus. Contact: John McCarthy, PhD, MPH VA Serious Mental Illness Treatment Research & Evaluation Center HSR&D Field Program / SMITREC PO Box 130170 Ann Arbor, MI 48113-0170 Email: John.McCarthy2@va.gov, mccarthy@umich.edu

Appleton - Project Manager (medical device experience needed)

PROJECT MANAGER – Core Team Leader Nellcor Puritan Bennett is now the Respiratory and Monitoring Solutions business unit of Covidien (formerly Tyco Healthcare) has relocated its operations to beautiful Boulder, CO. Our systems are used to monitor, diagnose and treat respiratory disease and sleep disorders, and they provide life sustaining ventilation and oxygen support for patients. In addition, to Respiratory and Monitoring Solutions, Covidien also manufacturers, distributes and services a diverse range of industry-leading product lines, including surgical devices, energy-based devices, pharmaceutical products, imaging solutions, patient care and safety products, and medical supplies. For more information and to apply online, visit us as www.covidien.com/careers Our jobs are now listed as "Respiratory Solutions" - Boulder, CO. We offer relocation assistance; a stable company with an excellent team environment and competitive salary and benefits! JOB DESCRIPTION Covidien, a leading Medical Device Company is looking for an energetic, organized, and motivational Core Team Leader. The individual will be responsible for managing a number (typically 2 or 3 at a time) of product development projects. They will manage and lead a group of highly skilled and multi-discipline team members toward the successful execution of business objectives. The Core Team Leader is responsible for the planning, scheduling and execution of engineering and product development related projects. Deliverables include engineering design output as well as documentation to be developed in the framework of FDA Quality System Regulations. The Core Team Leader is responsible for the creation of Work Breakdown Structures, General Development Plans and Product Requirements. He/She manages day-to-day activities of team members, tracks progress against plan, manages the project budget, identifies project risks, provides plans to mitigate those risks, provides periodic updates on the project to the business, and successfully completes periodic project reviews. TYPICAL RESPONSIBILITIES/DUTIES • Business level focus on details – leading cross functional team members Track day-to-day activities through email, telephone, face-to-face; some travel required. • Responsible for planning resource requirements and negotiating team resource assignments with functional managers • Proven ability to successfully track progress to requirements and plan; resolve deviations • Acts as information conduit between senior management and team members; prepares and presents monthly updates and project reviews on team’s behalf • Ability to negotiate, resolves conflict, and drive consensus among team members to accomplish project and business goals • Ensure compliance to internal Design Control procedure and business processes • Hold regular team meetings to communicate goals team-wide and track progress • Monitor risk and plan mitigations to risk to maintain business and project objectives QUALIFICATIONS • BSEE/ME, BA or equivalent; PMI certification and/or training is highly desirable • 8+ years of combined program management, product development experience and project management experience • Ability to manage and deliver results in a cross functional environment • Medical device industry/ FDA experience required • Experience with the development of complex systems containing electronics and/or software • Demonstrated strong written and verbal communication skills • Successful experience managing development projects • Experience and knowledge of systems • Proficient with Microsoft Project and MS Office Covidien is an Equal Opportunity Employer. Please note: This is NOT a capital equipment or IT function. This involves project work around several medical device product lines that incorporate electro-mechnical, optical, embedded complex systems. Thanks.

Asheville - Senior Chemist-BS

Our client is looking for a Senior chemist to lead QC Lab of leading pharmaceutical company in North Carolina. * BS in chemistry *5 years pharmaceutical/biotech industry experience * 3 years managing staff/technicians and chemists *Experience in Quality Control *Knowledge of validating test methods *Experience with HPLC and ELISA assays *Immunochemistry Assay experience *Must have experience with creating SOP’s in an FDA regulated environment *Knowledge of cGMP’s and FDA guidelines essential *Must be able to troubleshoot equipment issues and individual assays *Must be able to test and resolve issues with finished products *Responsible for leading activities of lab staff and producing reports and production summaries * Clear and effective written and oral communication skills *Attention to detail *Varian HPLC and Blue Mountain Calibration Database software experience is a plus. Must reside in the US and have current work visa or citizenship. Qualified candidates only please.

Asheville - Regional Clinical Research Associate

Please email your resume if you are interested in being contacted for an interview. Requirements: A minimum of 2 years experience as a regional CRA, more is better. 4 year degree 60 % travel 70-90K, outstanding benefits Thank-you for your time and interest!

Asheville - Line Manager

PAREXEL International Corporation is a leading global bio/pharmaceutical services organization, providing a broad range of knowledge-based contract research, medical marketing and consulting services to the worldwide pharmaceutical, biotechnology and medical device industries. Committed to providing solutions that expedite time-to-market and peak-market penetration, PAREXEL has developed significant expertise across the development and commercialization continuum, from drug development and regulatory consulting to clinical pharmacology, clinical trials management, medical education and reimbursement. Headquartered near Boston, Massachusetts, PAREXEL operates in 55 locations throughout 43 countries around the world, and has over 6,315 employees. For more information about PAREXEL International visit www.PAREXEL.com. Description: Responsible for organizing and managing all clinical data management activities on the company's largest and most complex projects including large teams and multiple protocols. Requires no supervision. Ability to solve problems using logical and systematic approaches is critical. Must thoroughly understand coding concepts, review of electronic data, medical encoding, SAE reconciliation and codebook applications. Must have solid understanding of therapeutic indications and study hypothesis. Acts as consultant with CDM's and teams for any and all data management issues and represents department at client meetings and presentations. Possesses in-depth knowledge in all areas of data management (coding, labs, SAE reconciliation, data validation manager, data validation specifications, tracking systems, Electronic Data Capture, or CRF Design). Makes recommendations for improvement of SOP's and WWP's resulting in streamlined processes and increased productivity. Experience: Education: BS/MS in health related or science discipline 2 year RN degree Minimum Work Requirements: Minimum of 4-8 years data management, clinical and/or research experience with solid understanding of clinical trials methodology and terminology Skills: Effectively applies technical knowledge to solve problems - Ability to provide advice or solutions based on expertise in technical areas to both internal groups and clients - Proactively seeks and takes action before being asked or the situation requires it - Ability to distinguish when an internal or external sign-off is necessary - Ability to determine when and how to escalate appropriate critical issues Offers support and constructive feedback to project team members please email resume to dorothy.hughes@parexel.com

Asheville - Sales Representative

What We Do Brinkmann Instruments, Inc. is the US regional office of world-renown Metrohm AG (Herisau, Switzerland), an industry leader in laboratory instruments and accessories for titration and electrochemistry research. Located in Westbury, (central) Long Island, New York, we are responsible for supporting all US and Canada sales, marketing, service and distribution activities. In addition to Metrohm products, our Sales and Marketing teams also represent equally renowned manufacturers, including Lauda, KINEMATICA and others, of high quality tools and equipment for chemical and industrial research and testing. Our innovative, high quality products are found in laboratories of all kinds—academic, industrial, research, quality control, processing, manufacturing and scale-up—and all are designed to help meet practical, scientific and economic goals. Brinkmann companies in North America include Brinkmann Instruments, Inc., in the US and Brinkmann Instruments Canada Corp. in Canada. As part of a global company and growing entity you will be part of a progressive and high-energy team, focused on bringing quality products to market and excelling in quality customer service. We are an Equal Opportunity Employer, offering competitive salaries and an attractive health and benefits package. Sales Representative Job Description * Travels throughout South Carolina, and parts of NC and TN to create demand for the company's products * Demonstrates product samples to end user customers * Trains distributor personnel on proper function and usage of selected Brinkmann products * Attends trade exhibits for the purpose of promoting products * Maintains company customer files in current database Skills and Education * Bachelor's degree (B.S.) from a four-year college or university; and one to two years' related sales experience and/or training, or equivalent combination of education and experience * Chemistry background strongly preferred * Must be computer literate and a self-starter with excellent communication skills Why Work for Us? You will be working in a professional, corporate environment. In return for your contributions, you will receive a competitive salary and an excellent company paid benefits package. A sampling of our company paid benefits include: * comprehensive medical * comprehensive dental * basic life insurance * accidental death and dismemberment * short and long term disability * tuition reimbursement program * paid vacation * paid holidays * paid sick and personal days * 401k plan * profit sharing plan * plus more! This position includes a company car and a complete technical sales package - laptop, Blackberry, etc. Brinkmann Instruments, Inc. is an equal opportunity employer. M/F/V/H

Asheville - *** High pay sales!!! ***4778998

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Athensga - Consulting Ontologist

Ingenuity is a group of creative, energetic and motivated people helping life science researchers understand core biological mechanisms. We deliver systems biology expertise to biologists and bioinformaticists through pathways analysis software, genome-scale computable network datasets, and knowledge management services and infrastructure, resulting in increased R&D productivity and faster drugs to market. We are passionate about our products, and dedicated to providing researchers with the knowledge required to make Better Decisions Faster™. As a Consulting Ontologist you will contribute to building Ingenuity’s Knowledge Base. This position is off-site (work from home), and training is provided. Key Responsibilities: •Research and identify biological concepts from the scientific literature •Represent and connect biological concepts in Ingenuity’s Ontology Education, Experience, and Skills REQUIRED: • BA/BS in a biological discipline (Molecular Biology, immunology, genetics, biochemistry or other related field) •Detail-oriented • Strong logic skills • Internet savvy • Familiar with Microsoft Office tools • Maintain a minimum level of productivity (about 10 hrs/week) Must be legally able to accept consulting work in the US Education, Experience, and Skills DESIRED: •Completion of graduate level coursework is a plus •MS degree, PhD candidacy or PhD degree is desirable •Research experience is a plus

Athensga - Laboratory Supply Sales

Expanding our sales force and looking for experienced laboratory and chemical sales representatives. We are a rapidly growing eleven-year-old scientific supply distribution company doing business with today’s technology with the “good old boy” approach. We are flexible to meet customer needs. We distribute the widest range of laboratory supplies and chemicals and can meet all our customer needs. This is a commission only position with no cap on what you can make. The representative will carve out their own territory based on familiarity to customers and relationships developed. This position is for a fulltime rep or we invite anyone experienced in the industry looking to supplement his or her income as an optional opportunity. Qualifications will require previous sales experience in laboratory, scientific, chemical or related industries. Send your resume and the area you reside in to labrep@yahoo.com.

Athensga - Teach MCAT - $40/hr

Examkrackers, Inc. is a test preparation company with a passion for excellence. We are currently looking for instructors to teach our Medical College Admissions Test (MCAT) preparation classes. The position is part time in the evenings from 4 to 16 hours per week. Talented, first-time teachers can earn up to $40/hr. The science knowledge required is at the first year undergraduate level; however, the test questions use a holistic approach and require a deep understanding of the subject matter. The students are highly motivated premeds making the instructor's job both challenging and rewarding. We strive to make any association with our organization a pleasurable and rewarding experience whether you're an instructor or a student. Requirements: Applicants must be passionate about teaching and about the subject matter. Applicants must have a thorough understanding of any or all of the following: 1st year undergraduate biology including some physiology; 1st year undergraduate organic chemistry; 1st year undergraduate inorganic chemistry; 1st year undergraduate physics. Applicants must be reliable, punctual, organized, and enthusiastic. Applicants with a strong MCAT score are highly preferred. Interested applicants should send a resume and MCAT scores to jobs@examkrackers.com

Athensohio - Consulting Ontologist

Ingenuity is a group of creative, energetic and motivated people helping life science researchers understand core biological mechanisms. We deliver systems biology expertise to biologists and bioinformaticists through pathways analysis software, genome-scale computable network datasets, and knowledge management services and infrastructure, resulting in increased R&D productivity and faster drugs to market. We are passionate about our products, and dedicated to providing researchers with the knowledge required to make Better Decisions Faster™. As a Consulting Ontologist you will contribute to building Ingenuity’s Knowledge Base. This position is off-site (work from home), and training is provided. Key Responsibilities: •Research and identify biological concepts from the scientific literature •Represent and connect biological concepts in Ingenuity’s Ontology Education, Experience, and Skills REQUIRED: • BA/BS in a biological discipline (Molecular Biology, immunology, genetics, biochemistry or other related field) •Detail-oriented • Strong logic skills • Internet savvy • Familiar with Microsoft Office tools • Maintain a minimum level of productivity (about 10 hrs/week) Must be legally able to accept consulting work in the US Education, Experience, and Skills DESIRED: •Completion of graduate level coursework is a plus •MS degree, PhD candidacy or PhD degree is desirable •Research experience is a plus

Athensohio - Regional Clinical Research Associate

Please email your resume if you are interested in being contacted for an interview. Requirements: A minimum of 2 years experience as a regional CRA, more is better. 4 year degree 60 % travel 70-90K, outstanding benefits Thank-you for your time and interest!

Atlanta - Senior Chemist

Senior Chemist – Laboratory Manager – Materials Testing Laboratory A materials testing and failure analysis laboratory in Marietta seeks equity partners able to expand our capabilities and carry shared management and technical responsibilities. The right individual will have experience and expertise that dovetails well with our current personnel and resources that may include industry contacts and an established client base. Financial investment is required as is active participation in exchange for co-ownership of our established and growing laboratory services and consulting company. Our concept is similar to that of medical or dental practices where office resources and personnel are shared. For professional scientists, our tools are expensive and sharing resources such as scanning electron microscopy, optical microscopy, conference areas, inspection facilities, physical testing, machine shop and chemical analysis equipment makes sense. Technical synergy is considered a significant advantage as well. You must be well educated, highly experienced, energetic, self motivated and conduct yourself with absolute integrity and professionalism. We are committed Christians and as such recognize the Biblical requirement in 2 Corinthians 6:14 for us to partner with other committed Christians only. While you would become an employee, we are not just looking for employees, nor for silent investors, so please don’t waste time by contacting us if you do not meet the expressed requirements and are not prepared to consider an active business partnership. Please do not call, but rather e-mail a letter and resume.

Atlanta - Medical Technologist

Seeking Medical Technologist to assist the manufactuirng, processing, and testing of biological samples. Must be able to perform various testing procedures on blood and serum products. Will utilize other skills to include troubleshooting, validations and problem solving. BS in Life Sciences with MT (ASCP or NCA certification). Minimum 1 year of laboratory expeirence.

Auburn - Regional Clinical Research Associate, 70-90k

Please email your resume if you are interested in being contacted for an interview. Requirements: A minimum of 2 years experience as a regional CRA, more is better. 4 year degree 60 % travel 70-90K, outstanding benefits Thank-you for your time and interest!

Augusta - Regional Clinical Research Associate, 70-90k

Please email your resume if you are interested in being contacted for an interview. Requirements: A minimum of 2 years experience as a regional CRA, more is better. 4 year degree 60 % travel 70-90K, outstanding benefits Thank-you for your time and interest!

Augusta - Laboratory & Chemical Supply Sales

Expanding our sales force and looking for experienced laboratory and chemical sales representatives. We are a rapidly growing eleven-year-old scientific supply distribution company doing business with today’s technology with the “good old boy” approach. We are flexible to meet customer needs. We distribute the widest range of laboratory supplies and chemicals and can meet all our customer needs. This is a commission only position with no cap on what you can make. The representative will carve out their own territory based on familiarity to customers and relationships developed. This position is for a fulltime rep or we invite anyone experienced in the industry looking to supplement his or her income as an optional opportunity. Qualifications will require previous sales experience in laboratory, scientific, chemical or related industries. Send your resume and the area you reside in to labrep@yahoo.com.

Bakersfield - Field Project Implementation Manager - Municipal Wastewater & Water

Field Project Implementation Manager-Wastewater & Water Facilities ****Please Tell Your Friend/Associates About This Position!**** -Top Pay, Outstanding Working Environment for Great Talent- Field Project Implementation Manager - Municipal Wastewater & Fresh Water Facilities Talented, Self-Motivated Help Wanted for Field Project Implementation Manager Wastewater/Fresh Water Facilities Upgrade Implementation Please Send Resume and Cover Letter to: HR.ProjectManagement@gmail.com Start Date: ASAP Salary range: $50k - $75+k/year, DOE - Outstanding Benefits! Leading Seattle-based west coast engineering firm has an immediate opening for a dynamic, resourceful Field Project Implementation Manager for municipal wastewater and fresh water facilities upgrade projects. This position requires a thorough knowledge of the principles and practices associated with PLC/SCADA/electrical/mechanical elements in municipal/district public works wastewater and or fresh water systems related to system process controls. This is an outstanding position for a detail-oriented, resourceful self-starter with good people skills. There is excellent opportunity for growth and advancement for someone with a "get it done" mindset. Sense of humor is a must. Responsibilities: • Work with the in-house engineering team to develop and implement wastewater and freshwater upgrade projects. • Manage site work done by vendors and contractors, ensuring the highest standards of quality and service are met or exceeded, • Work with vendors and contractors regarding bids, schedules and budgets • Maintain up-to-date and complete project records, track project timetables to ensure expedient, high quality implementations • Assist with implementation "on the ground.” Understand process electrical, mechanical, PLC and SCADA systems. Adept problem-solving abilities to meet challenges as they arise. • Attend internal and external project development and implementation meetings as required. • Maintain excellent working relationships with municipal/district management and staff. • Reports directly to company ownership/senior management. • Average two weeks per month regional travel devoted to contract sites to oversee and assist with project implementations. Qualifications: • Knowledge of current municipal/district wastewater and or freshwater practices and processes, as well as insight into challenges arising as upgrades are required. • Experience effectively working with municipal/public works management and staff. • Experience in project budgeting, scheduling and implementing municipal water projects. • Experience in working with/overseeing subcontractors and vendors. • Excellent written and oral communication skills. • Knowledge and use of MS Office software. • Solid experience with wastewater/ fresh water processes, control logic, PLC programming, and industrial automation in general, is highly desirable. While not necessary, engineering, project management or equivalent project experience in a municipal or public works setting is a plus. • Valid driver's license, good driving record, insurance. Salary is DOE and VERY strong compensation package includes: medical, dental, paid vacation, 401K. Please forward your resume, cover letter and job goals via e-mail to: HR.ProjectManagement@gmail.com -Seattle Waterfront Offices - Beautiful Setting

Bakersfield - Considering a career change? Become a Financial Representative

Northwestern Mutual Financial Network is looking to grow over the next 12 to 18 months in our Bakersfield office. We are looking to bring on a Financial Representative with a drive to build a career path in financial services. Someone with a strong drive to succeed, help make an impact on their client's lives, but also have the flexibility of owning and managing your own schedule. The opportunity to earn great income while also benefiting from seeing the impact your efforts can make on the community has never been greater! Financial Representatives offer guidance, relationships and solutions to help clients meet financial goals and objectives. They offer exclusive access to insurance products from a top-rated company, Northwestern Mutual, and an array of quality investment choices. Supported by training programs and mentoring opportunities, they have access to the resources, products and assistance they need to help clients and build their practices. As you build your business as a Financial Representative, you will: Meet With Clients — You'll set up appointments to discuss your clients' financial goals and current financial situation. Analyze the Client's Situation — After extensive fact-finding, you'll uncover long term goals that you will use to help determine your client's needs. Make Recommendations — After evaluating your client's current situation and goals, you'll determine what products can help fill their needs and present appropriate solutions to your client. Provide Ongoing Service — You'll continue to work with your clients beyond the close of the sale. Most Financial Representatives contact their clients twice per year to determine whether their needs have changed, and keep them aware of the resources available to them. Overview: Since 1857, Northwestern Mutual has consistently focused on one ambition: to do the right thing for the people who put their trust in us. We exist to help our clients manage financial risk and achieve financial security through our insurance and investment products. Our products and services offer a network of solutions to address clients needs for financial security and protection, capital accumulation, asset distribution and estate preservation. Products and Services: The Northwestern Mutual Financial Network offers a personalized approach to providing customized financial solutions tailored to each client's individual needs. Financial Representatives provide needs-based analysis and financial solutions to help ensure a client's needs are met at every life stage. Financial Representatives work closely with clients to develop customized solutions that meet long-term financial goals and objectives. They offer exclusive access to insurance products from a top-rated company, Northwestern Mutual, as well as disability income insurance, and an array of quality financial products and services available through Network Partners. Accolades: As well as being a Fortune 500 company, Northwestern Mutual was selected in the March 2007 issue of Fortune® Magazine as both the “Most Admired Company in America” in our industry for the 24th consecutive year and as a "Most Admired Company in the World”. Our Financial Representatives have been hailed the best sales force in America, co-winner with Cisco Systems (July 2000 issue, Sales and Marketing Management Magazine). Northwestern Mutual was also named one of “America’s 50 Best Companies to Sell For” in 2006 by Selling Power Magazine (November/December 2005) and was recognized as one of the “50 Best Companies to Launch a Career” last year by BusinessWeek magazine (September 18, 2006). Our products consistently receive the absolute highest available ratings for financial strength from the four major rating agencies: Standard & Poor’s, Moody’s Investors Service, FitchRatings and A.M. Best

Bakersfield - Financial Representative

Northwestern Mutual Financial Network is looking to grow over the next 12 to 18 months in our Santa Barbara office. We are looking to bring on a Financial Representative with a drive to build a career path in financial services. Someone with a strong drive to succeed, help make an impact on their client's lives, but also have the flexibility of owning and managing your own schedule. The opportunity to earn great income while also benefiting from seeing the impact your efforts can make on the community has never been greater! Financial Representatives offer guidance, relationships and solutions to help clients meet financial goals and objectives. They offer exclusive access to insurance products from a top-rated company, Northwestern Mutual, and an array of quality investment choices. Supported by training programs and mentoring opportunities, they have access to the resources, products and assistance they need to help clients and build their practices. As you build your business as a Financial Representative, you will: Meet With Clients — You'll set up appointments to discuss your clients' financial goals and current financial situation. Analyze the Client's Situation — After extensive fact-finding, you'll uncover long term goals that you will use to help determine your client's needs. Make Recommendations — After evaluating your client's current situation and goals, you'll determine what products can help fill their needs and present appropriate solutions to your client. Provide Ongoing Service — You'll continue to work with your clients beyond the close of the sale. Most Financial Representatives contact their clients twice per year to determine whether their needs have changed, and keep them aware of the resources available to them. Overview: Since 1857, Northwestern Mutual has consistently focused on one ambition: to do the right thing for the people who put their trust in us. We exist to help our clients manage financial risk and achieve financial security through our insurance and investment products. Our products and services offer a network of solutions to address clients needs for financial security and protection, capital accumulation, asset distribution and estate preservation. Products and Services: The Northwestern Mutual Financial Network offers a personalized approach to providing customized financial solutions tailored to each client's individual needs. Financial Representatives provide needs-based analysis and financial solutions to help ensure a client's needs are met at every life stage. Financial Representatives work closely with clients to develop customized solutions that meet long-term financial goals and objectives. They offer exclusive access to insurance products from a top-rated company, Northwestern Mutual, as well as disability income insurance, and an array of quality financial products and services available through Network Partners. Accolades: As well as being a Fortune 500 company, Northwestern Mutual was selected in the March 2007 issue of Fortune® Magazine as both the “Most Admired Company in America” in our industry for the 24th consecutive year and as a "Most Admired Company in the World”. Our Financial Representatives have been hailed the best sales force in America, co-winner with Cisco Systems (July 2000 issue, Sales and Marketing Management Magazine). Northwestern Mutual was also named one of “America’s 50 Best Companies to Sell For” in 2006 by Selling Power Magazine (November/December 2005) and was recognized as one of the “50 Best Companies to Launch a Career” last year by BusinessWeek magazine (September 18, 2006). Our products consistently receive the absolute highest available ratings for financial strength from the four major rating agencies: Standard & Poor’s, Moody’s Investors Service, FitchRatings and A.M. Best

Bakersfield - Testing Technician I

NuSil Technology is a world leader in the manufacture and application of specialty silicones for the aerospace, healthcare, and electronics industries. ISO 9001 certified since 1994, NuSil operates state-of-the-art laboratories and processing facilities in California, Texas, and Sophia Antipolis, France. With more than 400 employees worldwide, NuSil specializes in providing on-site, in-person application engineering support. The Testing Technician I corrects routine problems; reports non-routine problems to manager; may test incoming raw materials; may test finished products; may assist in processing hazardous waste stream for disposal; responsible for preparing various products for testing per NuSil TMs; maintains established tracking system; maintains various equipment; operates test equipment; may, under the direct guidance of the QA Analytical Specialist, assist in setting up experiments, data collection, research and report writing. BA/BS in science-related field preferred, or equivalent from two-year college or technical school; or six months to one year related experience and/or training; or equivalent combination of education and experience. Computer literate (WORD/EXCEL). Familiar with lab equipment operation and set-up, experience working with chemicals and chemical reactions helpful. NuSil is an Equal Opportunity Employer and Affirmative Action Employer. M/F/D/V Applicants may apply online at our website at http://www.nusil.com

Bakersfield - Regional Clinical Research Associate I/II

Regional Clinical Research Associate I/II Job Description: The responsibility of the CRA I/II is to oversee the conduct of a Pharmaceutical clinical trial to insure the quality and integrity of data and safety and efficacy of the drug. In coordination with the team leader, exercise responsibility for project activities related to monitoring function. Interface with clinical investigators and other site personnel in order to carry out this responsibility. Required Experience: •Education: RN, relevant clinical experience or 4 year Life Science degree. •Minimum Work Requirements: 6 months of clinical drug trial field monitoring experience with a pharmaceutical, CRO, or device company for CRA I. For CRA II you must have at least 2 years experience. •All Therapeutical areas will be considered. You will go to the front of the line if you have Oncology, Cardiovasculor or HIV experience. •Skills: Ability to communicate with professional medical personnel. Understanding of the drug development process. Ability to complete tasks in an accurate and timely manner. •Physical Requirements: Ability to travel an average of 75% and be within one hour of a major airport. Other information: This position is with a large Clinical Research Organization (CRO). It is a home based position. You must have the required experience noted above. Please do not email me your CV if you are a lab tech, foreign MD or someone who “knows they can do the job”. I am sure you all are great people but I need experienced monitors.

Bakersfield - Senior Scientist Research Formulation

Senior Scientist Research Formulation Position based in La Jolla, CA JOB DESCRIPTIONThe responsibilities of this position involve interacting with scientists in Discovery and Pharmaceutical Sciences in order to enable formulation development of lead drug candidates. Evaluate physical and biophysical properties of organic compounds relevant to various routes of drug administration including oral, parenteral, and ocular. Communicate results, interpretations, and implications to drug discovery project teams. Design experiments to develop formulations for various routs of administration to animals and humans in Phase I clinical studies; with particular attention to candidates with poor solubility and permeability and parenteral delivery. In addition, design experiments to determine the stability of organic compounds in formulations, to detect and identify the decomposition products, and to achieve formulations with acceptable shelf-life. Initiate and maintain a research program that yields contributions of value both to Pfizer and to the pharmaceutics scientific literature. QUALIFICATIONSPh.D. in Pharmaceutics, Pharmaceutical Chemistry, Chemistry, Physical Organic Chemistry, or related discipline; or MS/BS with 5 experience. Demonstrated expertise in analytical and characterization techniques. Sophisticated ability to solve complex problems in physical chemistry or biopharmaceutics in relation to developing parenteral drug delivery systems and pre-clincal and clinical formulation development. Excellent oral and written communication skills, and the ability to effectively contribute to team-based decision making. Demonstrated ability to reduce new ideas to practice. Experience (3-5 years) in pre-formulation or discovery support is desirable and preferred. Desirable attributes: Unique skill set that is consistent with the function and mission of the Research Formulation group, such as specialized knowledge of colloidal chemistry or ocular drug delivery, modeling pharmacokinetic data, ability to propose and test mechanisms of drug degradation in dosage formulations, prediction of physicochemical properties, high-through put screening of physicochemical properties, solid-state pharmaceutics, etc.BENEFITSThroughout our 153 years, a legacy of caring for others has been at the heart of everything we do at Pfizer. This commitment is no less important when it comes to our employees. Pfizer wants to ensure that employees have resources to help them develop and succeed both in their careers and personal lives. One way we can achieve this is through our comprehensive benefits program, which offers employees and their eligible dependents the variety and flexibility to help address their needs at different stages in life.COMPANY PROFILEPfizer Inc discovers, develops, manufactures, and markets leading prescription medicines for humans and animals and many of the world's best-known consumer brands. Our innovative, value-added products improve the quality of life of people around the world and help them enjoy longer, healthier, and more productive lives. The company has three business segments: health care, animal health and consumer health care. Our products are available in more than 150 countries.Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the U.S. for Pfizer. Pfizer retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified U.S. workers. Individuals requiring sponsorship must disclose this fact.Please make sure to reference the Job ID: when submitting your resume. Other ways to apply: http://posttrak.arbita.net/cgi-bin/PostTrak.cgi?RefCode=R2849116906147

Bakersfield - Lab Analyst - Metals Department

Job Title: Lab Analyst - Metals Department City of Job: Bakersfield Zip Code of Job: 93309 County of Job: Kern Experience Required: 6 - 12 months Number of Openings: 2 Job Listing Close Date: 11/30/2007 Rate of Pay: $12.00 Shift: Day Duration: Long Term Hours Per Week: 40plus California Driver's License: C (passenger car) Status: Open Job Duties: LOCAL LABORATORY IS SEEKING AN ANALYST TO WORK IN THE METALS DEPARTMENT ON THE DAY SHIFT 8AM-5PM. REQUIREMENTS ARE B.S. DEGREE IN (SCIENCE, BIOLOGY,OR SOME RELATED FIELD), INTERESTED IN LAB ANALYST WORK PREVIOUS VOLUNTEER/SCHOOL LAB WORK IS A PLUS!! WILL NEED CLEAN CRIMINAL BACKGROUND CHECK AND PASS A LAB D/S. WILL BE ON YOUR FEET FOR A LONG PERIOD OF TIME NEED TO BE ENERGETIC ABOUT THE PROFESSION LONG TERM OPPORTUNITY. How to apply: Mail résumé to: Employer Depot, Inc Attn: Elsa Zermeno 5701 Truxtun Ave. Suite 220 Bakersfield CA 93309 Contact Phone: Employer Depot, Inc. (661)325-0200 Fax: Employers Depot, Inc (661)325-0222 E-Mail: zermenoe@employersdepot.com URL: www.employersdepot.com

Bakersfield - Lab Analyst - Organic Department

Job Title: Lab Analyst - Organic Department City of Job: Bakersfield Zip Code of Job: 93308 County of Job: Kern Experience Required: 1 years Number of Openings: 1 Job Listing Close Date: 11/30/2007 Rate of Pay: $12.00 hr Shift: Day Duration: Long Term Hours Per Week: 40plus California Driver's License: C (passenger car) Status: Open Job Duties: ENTRY LEVEL LAB ANALYST(INORGANIC DEPARTMENT)MUST HAVE A BACHELORS DEGREE IN BIOLOGY, OR SCIENCE. IF YOU ARE INTERESTED IN GETTING INTO THE FIELD THIS POSITION WILL BE EXCELLENT. WILL BE DAY SHIFT 8AM-5 MON-FRI POSSIBLE SATURDAYS, REPLY ASAP FOR CONSIDERATION DUTIES WILL BE EPA TESTING, QC FUNCTIONS, DOCUMENTING RESULTS, ORGANIC EXTRACTIONS WATER AND SALT SAMPLES. IF INTERESTED UPDATE YOUR RESUME AND CALL ME! MUST PASS COMPLETE CRIMINAL BACKGROUND CHECK! How to apply: Mail résumé to: Employer Depot, Inc Attn: Elsa Zermeno 5701 Truxtun Ave. Suite 220 Bakersfield CA 93309 Contact Phone: Employer Depot, Inc. (661)325-0200 Fax: Employers Depot, Inc (661)325-0222 E-Mail: zermenoe@employersdepot.com URL: www.employersdepot.com

Bakersfield - Director of Quality Assurance

Job Title: Director of Quality Assurance City of Job: Bakersfield Zip Code of Job: 93307 County of Job: Kern Experience Required: 3 years Number of Openings: 1 Job Listing Close Date: 11/30/2007 Rate of Pay: 60,000.00yr. Shift: Day Duration: Long Term Hours Per Week: 40plus California Driver's License: C (passenger car) Status: Open Job Duties: Must have a BS in Scientific Field, Microbiology preferred. Duties will include: oversees a variety of microbiological testing and analyses: testing water\air\steam sources, beverages, incoming raw materials, taking samples of raw materials. Testing includes yeast & molds, SPC, E.COLI, STAPH, SALMONELLA, LISTEIA and others. How to apply: Mail résumé to: Employer Depot, Inc Attn: Elsa Zermeno 5701 Truxtun Ave. Suite 220 Bakersfield CA 93309 Contact Phone: Employer Depot, Inc. (661)325-0200 Fax: Employers Depot, Inc (661)325-0222 E-Mail: zermenoe@employersdepot.com URL: www.employersdepot.com

Bakersfield - Quality Assurance Supervisor

Job Title: Quality Assurance Supervisor City of Job: Bakersfield Zip Code of Job: 93309 County of Job: Kern Experience Required: 1 - 3 yrs Number of Openings: 1 Job Listing Close Date: 11/30/2007 Rate of Pay: $14.00 - $16.00 DOE Shift: Day Duration: Long Term Hours Per Week: 40plus California Driver's License: C (passenger car) Status: Open Job Duties: Education: BS\BA degree in one for the following areas:Food science, Microbiology, Chemistry, Biology or related area. Computer literate: Microsoft word,excel,power point, outlook, Responsible for Q. A training,auditing, daily payroll, shift scheduling, sustaining compliance to HACCP, monitor daily audit production procedures including verification of code dates,scales,water level,plant GMP's. Occasionally would need to lift boxes up to 30lbs. How to apply: Mail résumé to: Employer Depot, Inc Attn: elsa Zermeno 5701 Truxtun Ave. Suite 220 Bakersfield CA 93309 Contact Phone: Employer Depot, Inc. (661)325-0200 Fax: Employers Depot, Inc (661)325-0222 E-Mail: zermenoe@employersdepot.com URL: www.employersdepot.com

Bakersfield - Testing Technician I

NuSil Technology is a world leader in the manufacture and application of specialty silicones for the aerospace, healthcare, and electronics industries. ISO 9001 certified since 1994, NuSil operates state-of-the-art laboratories and processing facilities in California, Texas, and Sophia Antipolis, France. With more than 400 employees worldwide, NuSil specializes in providing on-site, in-person application engineering support. The Testing Technician I corrects routine problems; reports non-routine problems to manager; may test incoming raw materials; may test finished products; may assist in processing hazardous waste stream for disposal; responsible for preparing various products for testing per NuSil TMs; maintains established tracking system; maintains various equipment; operates test equipment; may, under the direct guidance of the QA Analytical Specialist, assist in setting up experiments, data collection, research and report writing. BA/BS in science-related field preferred, or equivalent from two-year college or technical school; or six months to one year related experience and/or training; or equivalent combination of education and experience. Computer literate (WORD/EXCEL). Familiar with lab equipment operation and set-up, experience working with chemicals and chemical reactions helpful. NuSil is an Equal Opportunity Employer and Affirmative Action Employer. M/F/D/V Applicants may apply online at our website at http://www.nusil.com

Bakersfield - Experienced Clinical Research Associates

ICON Clinical Research is dedicated to providing the pharmaceutical and biotechnology industries with exceptional clinical research and biometrics services. Join us in one of our current openings and enjoy highly competitive benefits and exceptional advantages. Experienced Clinical Research Associates Responsibilities will primarily involve management of assigned investigational study sites including: pre-study, initiation, monitoring and study close-out site visits. Approximately 65% travel overall can be expected. In line with our philosophy of providing the highest quality to our clients, CRAs are typically assigned to one to two programs at a time and participate in continuous training. Applicants should possess a B.S. degree in the life sciences or nursing or an equivalent combination of education and work experience. Applicants must have at least 12 months of experience monitoring pharmaceutical clinical trials. Excellent communication and organizational skills are essential. An ICON CRA must be able to travel overnight, primarily in the USA, 3 days per week on average. Note: *Experienced Study Coordinators should apply for “Clinical Research Associate - Entry- Level” positions when such postings are advertised instead of this job posting *We are considering office-based and home-based CRAs. Home Based CRAs must have a minimum of two years of independent, multi-site management experience for the home based program. Come to ICON and be an important part of a well respected and growing company that believes the details of your career are every bit as critical as the work you do. You'll enjoy highly competitive benefits in addition to flexible scheduling, relocation assistance, tuition reimbursement, credit union, health club privileges, and many other exceptional advantages. For more information on our opportunities and locations, please visit us at http://www.iconclinical.com/index.asp?getpage=true&sid=10 .No agencies, please. ICON. A Symbol of Excellence. ICON Clinical Research is an Equal Opportunity Employer committed to strength in diversity. To Apply for this position, please CLICK HERE or send your resume to resume@iconsu.com.

Bakersfield - Adventurous Biologists

Adventurous biologists to observe and sample catches onboard commercial fishing boats off Alaska. Duties include collecting representative samples of the catch, sorting, recording and measuring different species, Requires B.S. in biology or natural sciences, a college level statistics course and a flexible attitude. Strenuous working conditions. Opportunities year around. Training provided. While onboard fishing vessels, biologists identify fish species and collect and record data on the sex, length and quantity for species caught. This fishery data is used by government agencies such as National Marine Fisheries Service (NMFS) and Alaska Department of Fish and Game (ADF&G) to manage commercial fisheries. Requirements: Bachelor's Degree in fisheries science or other biological science, college level statistics course, pass a physical exam, and must have U.S. Citizenship. Please email your current resume to apply to yani@saltwaterinc.com and visit our website at www.saltwaterinc.com. Questions please call Yani at 907-276-3241.

Baltimore - Director, Hematology/Oncology

Director, Hematology/Oncology–can be Assoc Dir or Exec Dir-cPharmaceuticalReference #: C-TL-0-4-795 (include reference number when responding) Job Requirements: All our positions require prior work experience at a pharmaceutical, biotech/pharma, or CRO (Clinical Research Organization). A medical degree from an accredited & internationally recognized medical school with a curriculum relevant to general medical education & training, Board Certification in Hematology/Oncology, along with a medical license to practice in the US is required. No clinical research experience required. Ability to establish & meet priorities, deadlines, & objectives. Skills in providing consultation & advice on multiple assignments required, as well as initiative & flexibility. ** Position will be filled at a level appropriate to one’s background – from an Associate Director level up to Executive Director level. MUST have pharmaceutical industry experience (or will also consider CRO experience).Job Description: The Medical Advisor participates in all aspects of Medical & Scientific Services' involvement on assigned trials. Provides medical support to investigative sites & project staff for protocol-related issues including protocol clarifications, inclusion/exclusion determinations, & issues of patient safety and/or eligibility. Performs review & clarification of trial-related Adverse Events (AEs). Performs medical case review of Serious Adverse Events (SAEs), including review of case documentation & patient narrative. Provides medical support for the Analysis of Similar Events (AOSE). Performs medical review of Adverse Event coding. Performs medical review of the protocol, Investigative Drug Brochure (IDB), and/or Case Report Forms (CRFs). Performs review of the Clinical Study Report (CSR) & patient narratives. Available 24 hours per day, 7 days per week to respond to urgent protocol-related issues at the investigative sites. Attends & presents at Investigator Meetings. Provides therapeutic area/indication training for the project clinical team. Attends meetings, as needed or requested. Serves as Scientific Advisor & provides guidance to Project Managers on the medical & scientific aspects of assigned projects.Please Note:We represent only professionals who have prior work experience in the pharmaceutical / biotech industry. All our positions are listed at www.landmarksearch.com. All our positions are permanent, full-time, office-based positions. Most positions have relocation assistance.Please email resume as a Word attachment to melissa@landmarksearch.com for confidential consideration for this and any of our other 141 positions in the pharma/biotech industry.We give you additional details about the company and the position after you submit your resume to us and after we review your career goals with you. To protect your confidentiality, your resume is NOT submitted to any of our client companies without your prior authorization.

Baltimore - Associate Director/Director, Medical Neurology-cPharmaceutical

Associate Director/Director, Medical Neurology-cPharmaceuticalReference #: C-TL-0-625 (include reference number when responding) Job Requirements: All our positions require prior work experience at a pharmaceutical, biotech/pharma, or CRO (Clinical Research Organization). US Board Certification in Neurology, research experience preferred; Doctorate of Medicine and 5 years experience in the medical and scientific fields in addition to 2 years clinical trials experience as an investigator or in the Pharma, CRO, or Biotech industry, or other comparable combination of training, education and experience. Highly effective verbal and written communication skills. Understands the need for effective and accurate communication. Highly effective interpersonal, organizational skills and leadership skills, including the ability to work within a matrix team environment. Demonstrated ability to lead and motivate a clinical team. Ability to handle management/personnel issues of medium to high complexity.Job Description: Management responsibilities including professional development, performance appraisals, and employee counseling for junior staff. Assigns work and reviews workload for all direct reports. Supervises staff by establishing goals that will increase knowledge and skill levels, and by delegating tasks commensurate with skill level. Approves courses of action on all management/human resources’ matters, including salary administration, transfers, hiring, terminations, professional development, performance appraisals, position description preparation, and employee counseling. Serves as Sub-Investigator including reviewing protocol objectives, executing protocol procedures, informing Primary Investigator about clinically relevant findings especially SAEs, etc. Reviews study problems/issues with study directors/team members and assists with facilitating prompt corrective action before, during, and after the study. Serves as departmental liaison to other divisions to promote cross-functional integration and harmonization. Maintains awareness of overall developments in the field through current literature, application of new technology, attendance at professional meeting etc., and ensures that immediate staff remains current on developments. Provides appropriate medical service for volunteer’s/patients participating in clinical studies.Please Note:We represent only professionals who have prior work experience in the pharmaceutical / biotech industry. All our positions are listed at www.landmarksearch.com. All our positions are permanent, full-time, office-based positions. Most positions have relocation assistance.Please email resume as a Word attachment to melissa@landmarksearch.com for confidential consideration for this and any of our other 141 positions in the pharma/biotech industry.We give you additional details about the company and the position after you submit your resume to us and after we review your career goals with you. To protect your confidentiality, your resume is NOT submitted to any of our client companies without your prior authorization.

Baltimore - QC Analyst II

Responsibilities: -General microbiology/cell culture, including bio-burden, bacterial & cell culture, LAL/endotoxin, and environmental monitoring -Execute established QC protocols and procedures (as outlined in SOPs) with minimal supervision -Develop and author Standard Operating Procedures (SOP) and associated documentation (material specifications, data sheets, etc) -Support routine QC release assays and other QC activities related to product release -Document, interpret and report assay results in a timely manner -Method development / technology transfer -Qualify, validate and maintain laboratory equipment -Collaborate effectively with internal/external customers

Baltimore - Analytical Scientist

Requirements: B.S. or M.S. in Chemistry, Analytical Chemistry, or related scientific field with minimum of 2 years of experience in separation and characterization of protein and nucleic acids. Experience with Agilent and Waters HPLC system is required. Experience in high performance liquid chromatography (HPLC) method development and validation is preferred. Familiarity with working in a regulated environment GxP and familiarity with current state of the art separation methodology are highly desired. Demonstrated problem solving skills, the ability to contribute to multidisciplinary project teams, excellent interpersonal and communication skills, and flexibility to succeed in a dynamic and changing environment are essential.

Baltimore - Senior Quality Control Specialist

The Senior Quality Control Specialist I is responsible for supporting the Quality Control Department through review and approval of test data, implementation of new assays and procedures and training of QC personnel Primary Role Responsibilities 1. Provide training for QC laboratory employees to perform testing and sampling procedures by following written SOPs. 2. Develops and conducts validation Protocols and prepares final Summary Reports independently to support the qualification and/or validation of test methodology following industry and company standards including, but not limited to ICH, USP or other pertinent regulatory guideline. 3. Develop protocols and summary reports to validate the installation, operation and performance of analytical equipment. 4. Assist entry-level employees in developing a thorough understanding of cGMP principles and ensure work performed by QC laboratory personnel is documented accurately and promptly. 5. Initiate investigations and corrective actions to address departures from written SOPs and write/revise Standard Operating Procedures to ensure accurate and efficient test methods. 6. Implement new procedures and policies. Transfer client methods into the laboratory and participate in client meetings when necessary. 7. Write monthly reports, summary reports and trend analysis reports. Quality Responsibility Maintenance of quality systems and cGMP compliance for the business by ensuring that all team members comply with processes, procedures and instructions for all activities in which the team participates. Safety Responsibility · Is knowledgeable and complies with all pertinent safety policies, rules and regulations. · Ensure that all team members comply with safety rules and regulations.

Baltimore - ENVIRONMENTAL ANALYST/SCIENTIST

ENVIRONMENTAL ANALYST/SCIENTIST - (Full-time direct hire position with benefits) Location: Annapolis, MD One of the area's premier Environmental consulting firms has an immediate opening for a mid-level Environmental Scientist to work in its Annapolis, Maryland, office. The successful candidate must have a Bachelor of Science degree from an accredited 4-year university, at least 2 years relevant professional experience, and the availability to travel at least 6 weeks per year (non-consecutive). Strong knowledge of NEPA is required This position involves overseeing environmental management systems, scheduling and coordinating Phase I ESAs (Environmental Site Assessments) and performing regulatory compliance audits. Secondary functions of this position include natural resource planning (wetland delineation, biological surveys) Company offers an exciting, casual work environment, and a competitive salary and benefit packages. Benefits include health insurance, disability coverage, 401(K) retirement plan, 3-weeks paid leave, and career growth opportunities. For consideration please e-mail resume to Paul Zaruba at pzaruba@theansellgroup.com

Baltimore - Microscopist

Education: B.S. Degree in Chemistry or Mineralogy or related degree and 7-10 years experience in materials analysis. M.S. Degree in Chemistry or Mineralogy or related degree and 5-7 years experience in materials analysis preferred. Responsibilities: Conduct laboratory experiments independently and in consultation with the Principal Scientist and project scientists. Record data, analyze, interpret and present results to project scientists via oral and written reports. Recommend next steps in progressing a project. Plan and prioritize independent research projects. Maintenance and organization of a safe and functional laboratory. Monitor, trouble-shoot and maintain laboratory equipment. Presentation of experimental results in a timely and organized manner. Prepare technical reports summarizing research results. Skills Required: Experience with analytical microscopy techniques such as light microscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM) and atomic force microscopy (AFM) required. Familiarity with sample preparation techniques such as sputter coating, microtoming, and embedding and polishing. Experience with capturing, processing and interpreting digital images. Strong laboratory organizational skills. Strong understanding of chemistry and mineralogy. Excellent oral and written communication skills. Computer skills (MS Office, Lotus Notes, SAP, imaging software.) Some travel (<5%) may be required.

Baltimore - Research Associate

Research Associate Essential Functions: Carry out standard operating procedures involving basic laboratory techniques, calculations, materials measurement, operation of laboratory equipment and record keeping necessary to perform assays. Record keeping includes but is not limited to Batch Data Records, notebooks, customer reports and work order documents. Make detailed observations and analyze data to ensure within operating parameters. Advise manager of factors that may affect quality of product testing. Suggest options / ideas for corrective actions. Complete, distribute and file records. Perform routine environmental monitoring of clean room areas during testing. Maintain accurate, up to date documentation (forms, logs, various records, etc.) related to supported systems. Material handling duties will include some receiving of materials from internal and external sources. Shipping materials between facilities. Distribution and transfers of internal materials. Maintain adequate inventory controls and documentation. Update inventory database as needed. May perform other related duties as required and/or assigned. Nature and Scope: This position largely interacts with equivalent levels of personnel in the biologics testing area. Good oral and written communication skills are required to identify problems and implement solutions in a team environment. Effectiveness in this role requires a functional knowledge of Invitrogen’s testing process and Standard Operating Procedures and the ability to see opportunities for improved effectiveness. The job encounters work situations of moderate scope and complexity and identifiable factors. Works on problems where analysis of situation or data requires a review of identifiable factors. Incumbent exercises judgment within defined procedures and practices to determine action. The incumbent normally receives general instructions on routine work and detailed instruction on new assignments. This is an entry-level position. Under limited supervision, this position is responsible for one or more of the following activities in BT-Microbiology including analytical testing, characterization, method development, and sample and data management. Specific responsibilities include planning and performing routine, and some non-routine, laboratory procedures, such as sample testing, standards preparation and testing procedures, compendial and non-compendial test methods, method development, and characterization, environmental monitoring and sampling during test sessions. Employees will also be responsible for reporting and evaluating backup/archive and trend analytical data. Additional responsibilities include providing and communicating results, troubleshooting equipment problems, and initiating and/or implementing changes in controlled documents. Employees will attend, participate, contribute, and present at departmental meetings. Employees must learn and comply with safety guidelines, GLP, and cGMPs/CFRs which includes, but is not limited to, the maintenance of training records, laboratory notebooks, written procedures, building monitoring systems and laboratory log books. The candidate will be working under clean room conditions within the areas of sterility and bacteriology Education: High school diploma, AA degree or Bachelor's Degree in Life Sciences or a related field or the equivalent combination of education and experience required. Experience: Requires 1- 5 years experience in the application of Microbiology laboratory techniques in a manufacturing environment or research laboratory. Demonstrated proficiency in the use of basic laboratory techniques, equipment and materials required. Demonstrated ability to carry out written scientific production instructions required. This position will require excellent aseptic technique, attention to detail, and good written and verbal communication skills. Timely and accurate completion of documentation is a must. Basic computer data entry skills are required. The candidate for this position should be flexible to handle a routine schedule with sometimes dynamic changes. Contacts: Has contact with equivalent levels of company employees Working Conditions: Works in a lab environment with specialized equipment. Employees will be required to operate automated and semi-automated equipment. The noise level in the work environment is usually moderate. Must be flexible to work varying schedules and hours as needed. The physical demands described above are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Education: High school diploma, AA degree or Bachelor's Degree in Life Sciences or a related field or the equivalent combination of education and experience required. Please send resumes in word format to christopher.wilkins@adeccona.com Adecco is an EOE

Baltimore - marketing Manager

PAREXEL International Corporation is a leading global bio/pharmaceutical services organization, providing a broad range of knowledge-based contract research, medical marketing and consulting services to the worldwide pharmaceutical, biotechnology and medical device industries. Committed to providing solutions that expedite time-to-market and peak-market penetration, PAREXEL has developed significant expertise across the development and commercialization continuum, from drug development and regulatory consulting to clinical pharmacology, clinical trials management, medical education and reimbursement. Headquartered near Boston, Massachusetts, PAREXEL operates in 55 locations throughout 43 countries around the world, and has over 6,315 employees. For more information about PAREXEL International visit www.PAREXEL.com. Barnett International, a division of PAREXEL, is widely recognized for its superior consulting services and its targeted education and training programs. Barnett helps clients get the most out of their research and development dollars by managing change effectively, improving organizational performance, and enhancing staff knowledge. We help pharmaceutical, biotechnology and medical device companies maximize the speed and quality of their product development efforts. With an international presence and with many staff members working from the client site for increased benefits, Barnett is able to apply a global expertise to its projects. Description: Barnett is looking for a Marketing Manager to manage all communication efforts that support the marketing planning and business development activities for all service lines of Barnett Educational Services. The responsibilities will include but are not limited to leading Barnett’s marketing efforts through the development and implementation of marketing plans for all of Barnett’s products and services, managing marketing vendors, interfacing with product development teams and developing and implementing strategies for growing Barnett’s marketing database and resources. Experience: Education: BS/BA in Marketing or business degree Minimum Work Requirements: 5+ years marketing experience, preferably in a business-to-business role Skills: Excellent oral and written communication skills; excellent project management and leadership skills; strong background marketing campaign planning and collateral development and creation; knowledge of pharmaceutical industry; excellent oral and written communication skills; strong interpersonal skills; strong MS Office skills; self motivated and ability to work independently and with a decentralized team. We have a casual, friendly, atmosphere promoting individual development and career growth. In addition, we offer a competitive salary, an excellent benefits package including tuition reimbursement, 401(k) and health insurance plans. PAREXEL is an Equal Opportunity Employer that develops strength through diversity. Please visit our web site at www.parexel.com. Please email resume to gladys.sistrunk@parexel.com

Baltimore - Manufacturing Supervisor

Responsibilities •Supervise the manufacturing group activities including bulk manufacturing, filling, labeling, and packaging operations, •Responsible for the creation and review of Quality documentation (ie. SOP’s, Batch Records, Testing Procedures, Deviations, etc.) and changes as well as technical reports. •Identification and implementation of improvement activities including but not limited to cost savings, efficiency gains, product quality, and documentation •Responsible for the review of completed Batch Records, equipment logs and production records prior to submission to QA •Follow SOP’s and cGMP guidelines to ensure product specifications are met. •Oversight of the maintenance of the manufacturing area to ensure GMP Audit Readiness •Responsible for Great Plains transactions including closing of shop orders, critical data entry, period ending activities •Ensure that manufacturing processes and procedures are up to date and effective. •Review and train technicians to perform validations related to quality initiatives, manufacturing scale-up and automation integration •Assist with qualifying alternate vendors for key raw materials, including identifying vendors, determining specifications, performing laboratory experiments and analyzing results •Participate in the transfer of new product and process improvements from product development to manufacturing, including writing/revising related SOP’s •Develop and maintain process databases and schedules for manufacturing operations •Responsible for training new personnel on proper production practices/procedures •Responsible for the completion of manufacturing employee reviews •Other related duties as assigned Education •BS degree in a biological field Experience •Strong knowledge of basic laboratory procedures, equipment, processes •2+ years prior experience working in a cGMP manufacturing laboratory •Must possess strong motivational skills and the ability to develop a strong team environment •Must posses effective written and oral communication skills •Knowledge of reagent processes, laboratory and production procedures •An understanding of and proficiency in the use of PC applications such as Microsoft Word, Excel Supervisory Responsibilities •Direct oversight of all manufacturing technicians Work Environment: Open office environment