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Baltimore - Various Space Department Opportunities

We are excited to announce that we have a volume of openings within our Space Department due to several new awards received in our Civilian Space and National Security Space Business Areas. Positions Available: -Propulsion System Engineer -Senior Structural Analysis and Test Engineer -Mission Operations Analyst, MSX -Senior Orbital Dynamist and Mission Manager -Mission Applications Developer -Spacecraft RF Communications Engineer -Satellite Ground Station Lead Engineer -Senior Packaging Engineer -Mission Design or Navigation Engineer -Guidance and Control Engineer -Radiation Test and Evaluation Engineer -Analog, Digital, RF and Mixed Signal Test Engineer -Senior Material Control Planner -Spacecraft System Engineer -Descent and Landing System Engineer If you are interested in one or more of these opportunities, please send us your updated resume. Include the titles of the positions you would like more detail on. We look forward to working with you!

Baltimore - Environmental Health Aide III

ENVIRONMENTAL HEALTH AIDE Howard County Health Department, Bureau of Environmental Health is recruiting for a full-time contractual Environmental Health Aide III. This position will assist in bureau scanning projects, field locating of drinking water wells utilizing GPS equipment, data entry and assisting with pool and spa inspections. Position requires graduation from a standard high school, or possession of a high school equivalence certificate and four years of experience in sanitation or closely related field. Education at an accredited college or university may be substituted for the required experience at the rate of 30 semester credit hours for each year. Salary is $11.83 - $13.59 per hour based on education and experience. Must have valid Maryland driver’s license. Send MS-100 (State Application) to V. Michie, HCHD, 7178 Columbia Gateway Drive, Columbia, MD 21046. To obtain a state application go to www.howardcountymd.gov. Open until filled. EOE.

Baltimore - Medical Writer/ Manager (Regulatory)

We are currently experiencing clinical success and have a rapidly growing clinical department. We are actively hiring experienced Sr. Medical Writers for a crucial role in our continued success and growth. Job Description: 1. Principle activity will be the organization and formatting of regulatory filings in CTD format 2. Work closely with CROs and internal Pre-Clinical, Clinical, Manufacturing and QA staff in the coordination and preparation of documentation to support regulatory filings 3. Advise teams on the timelines and process for regulatory submissions publishing 4. Write, revise, and format preclinical and clinical documents for submission to global regulatory agencies 5. Prepare and maintain submission tracking documents and monitor status of submission components 6. Maintain up-to-date knowledge of FDA standards and procedures for regulatory submissions, including eCTD; analyze new and revised guidances, advise management of new requirements 7. Drive improvements in corporate document templates and Style Guide 8. Evaluate and implement company regulatory publishing systems/mechanisms, document management system and regulatory software tools and templates 1. Bachelors degree in scientific discipline (Graduate degree desirable) 2. Medical writing experience in established pharmaceutical company or CRO of 8 or more years 3. Experience in the coordination and filing of regulatory documents including CTAs, INDs and NDAs, in the CTD format. Experience with eCTD a plus 4. Expertise in Word and in editorial and publication software programs 5. Highly organized and able to effectively multi-task; strong project management skills 6. Possess excellent communication and negotiation skills

Baltimore - Chemist (microscopist)

We are actively recruitng for a Physical Chemist in our Baltimore Research Facility. This is a full time, permanent opportunity to work for an established and still growing organization with a reputation for success. 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. 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.

Baltimore - Manufacturing Supervisor

We are a growing biotech company with a strong product that has been doubling in production for the past two years. We are looking for an experienced Manufacturing Supervisor or Lead Technician who has the desire to contribute to the success of our organization. • 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 • A minimum of 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

Baltimore - Lab Technician

Responsibilities • Perform bulk manufacturing, filling, labeling and packaging operations • Follow SOP’s and cGMP guidelines to ensure product specifications are met • Perform shipping and receiving activities • Perform quality control activities on raw material and manufactured products, including analyzing and interpreting results • Assist with validation related to manufacturing scale-up and automation • Assist with qualifying alternate vendors for key raw materials, including identifying vendors, determining specifications, performing laboratory experiments and analyzing results • Assist with transfer from product development to manufacturing, including writing related SOP’s • Cross-functional technical responsibilities in product development including processing patient samples and analyzing results Education • BS degree or equivalent laboratory experience Experience • Knowledge of basic laboratory equipment • Prior experience working in a cGMP laboratory • Knowledge of reagent processes, laboratory and production procedures

Baltimore - Chemist

The successful candidate will work in collaboration with a team of analytical scientists in a multidisciplinary analytical problem solving environment for the analysis, review, and documentation of analytical data in compliance with regulatory, GxP, and departmental SOP requirements. The candidate will investigate and evaluate new, innovative approaches within the field of separation sciences to support the new product research and development and product process improvement. Position 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 - Validation Engineer

Description: Three to five years hands-on CSV experience (developing / authoring CSV documents) in an FDA regulated quality control or R&D environment for a major commercial LIMS package (E.g. SampleManager, LabWare, SQL*LIMS, STARLiMS, LabVantage). Global LIMS implementation a plus. Solid understanding of theory and concepts in use of lab informatics system functionality to support laboratory processes in pharmaceutical R&D or QC environments required. ** Strong oral and written communication skills. ** Working knowledge and understanding of concepts and FDA regulations as they apply to use of lab informatics applications and laboratory equipment in regulated environments, in particular 21 CFR Part 11. ** Self motivated, able to work / follow project plan independently, with minimal supervision. Participate in and support the execution of validation activities. Co-ordinate with IT to develop IQ and end users to generate OQ/PQ Lenience for working in dynamic project setting with changing priorities and schedules, aggressive project schedules. Term: approximately 6 months Location: Maryland Start Date: Approximately 1st week of January 2008 Education: Minimum of Bachelor’s Degree

Baltimore - 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!

Baltimore - THE MARYLAND SCIENCE CENTER- SEEKING APPLICANTS

A great downtown location right on the water. Easy access from major roadways and mass transit. A place to showcase your talents. A place where guests learn and have fun. These are just some of the reasons why employment at the Maryland Science Center can be one of the most rewarding, challenging, and interesting opportunities available to you. The Maryland Science Center is currently seeking qualified candidates for a number of seasonal positions, as well as full and part time year-round positions. For more information and to apply, please visit our website at www.marylandsciencecenter.org AVAILABLE JOBS FULL TIME POSITIONS Assistant Producer/Education Coordinator Housekeepers Maintenance Technician Outreach Specialist SpaceLink Manager PART TIME POSITIONS BodyLink Staff Kids Room Staff Observatory Presenter Planetarium Console Operator Public Programmers SpaceLink/TerraLink Presenter School Programs Instructor Ticket Agents

Baltimore - Research Associate

We are a biopharmaceutical company that is developing products that are delivered directly to the site of tissue injury, preemptively inhibiting inflammation, pain and other problems associated with medical and surgical procedures. Our products are designed to act on distinct molecular targets at the site of delivery, providing improved therapeutic benefit while minimizing the risk of side effects. We are working on a pipeline of products for use in orthopedics, urology, cardiovascular medicine, general surgery and pain management. Benefits of working for us include pre-IPO stock options and competitive salary. Responsibilities: • Perform routine site visits, including pre-study, initiation, interim and closeout visits. Performs responsibilities with minimal support from management. Visits to include monitoring of proper informed consent procedures, compliance with protocol, GCP/ICH Guidelines and other applicable regulatory requirements, and assurance of good site performance. This is accomplished by detailed review of subject records, essential documents, investigational product disposition and accountability, site personnel and procedures. • Manage assigned sites by regular contacts to ensure site compliance, adequate enrollment, and understanding of study requirements. • Report to project team and site personnel any findings noted at monitoring visits. This is accomplished by completion of monitoring reports and follow-up letters within the project-specific timelines. Significant issues noted must be reported to appropriate personnel immediately. • Maintain project tracking system of subject and site information. • Participate in company-required training programs. • Perform necessary administrative functions (e.g., tracking of expense reports, time and attendance). Qualifications • Bachelor's level degree in life sciences, pharmacy, nursing or RN preferred • 2+ years clinical monitoring experience, including field monitoring, site and study start up and management, experience in drug/device development • In-depth Knowledge of Good Clinical Practices (GCP's), ICH Guidelines, FDA regulations and other applicable regulatory requirements • Strong leadership skills • Ability to work independently in a fast-paced environment • Strong communication, interpersonal, and organizational skills • Must demonstrate good computer skills • Position requires approximately 60% travel (may be up to 80% during peak times) Required Skills -------------------------------------------------------------------------------- Clinical Research Associate, Biopharmaceutical, GCP Good Clinical Practices, ICH, Monitoring If you are a good fit for the Midwest Regional Clinical Research Associate - Biopharma position, and have a background that includes: Clinical Research Associate, Biopharmaceutical, GCP Good Clinical Practices, ICH, Monitoring and you are interested in working the following job types: Biotech, Pharmaceutical, Healthcare Within the following industries: Pharmaceutical, Biotechnology, Real Estate - Property Mgt Our privacy policy: Your resume and information will be kept completely confidential. Looking forward to receiving your resume through our website and going over the job in more detail with you! Apply online by reviewing the job listing at: http://www.bioemployment.com

Baltimore - Lab Glassware Washer

Position:Lab Glassware Washer Location:Reisterstown, MD Salary:$14.00 Per Hour Terms:Fulltime, Long-Term Contract Position Hours:Monday-Friday, 8:00am-4:00pm (possibility of overtime) Great entry level opportunity for those interested in lab work or the scientific field Responsibilities: •Keep glassware and lab materials clean by hand washing as well as operating glassware cleaning machines Necessary Skills: •Basic computer skills Qualifications: •Must be able to lift up to 50lbs •Solid work history •Past lab or scientific background is required •Criminal background check and Pre-employment drug testing required for this position

Baltimore - Clinical Project Manager

.. Function as primary liaison between sponsor and staff and as primary contact for project issues, including the planning and execution of protocol-specific deliverables and managing of budgets. b.. Establish objectives and strategies to direct activities, evaluate capabilities, plus track, measure, and report the status of project milestones. c.. Oversee day-to-day activities of team members; work closely with sponsor team members to ensure timely and accurate reporting of critical information. d.. Identify critical project tasks/issues and recommend/implement courses of action to expedite project objectives. e.. Review and update revenue projections based upon project plan and proposal fees; trigger invoicing processes; initiate change-in-scope amendments. f.. Conduct regular Project Team Meetings including distributing action items with assignments and due dates. g.. Review business development proposals. h.. Travel locally and nationwide as needed. Qualifications: a.. B.S. degree in nursing, pharmacy, or the life sciences; advanced degree preferred. b.. Minimum of 3-5 years related experience in the pharmaceutical industry or a CRO including project management and staff supervisory expertise. c.. Thorough knowledge of the pharmaceutical clinical drug development process and team-based matrix management. d.. Thorough knowledge of Good Clinical Practices (GCPs). e.. Ability to effectively manage client relationships and client expectations. f.. Ability to effectively guide and lead teams to achieve desired results within timelines and budget commitments. g.. Ability to manage multiple tasks concurrently.

Baltimore - Human Subject Protection Scientists

AMDEX Corporation is seeking professionals with a minimum of a Bachelor's Degree in the Health Sciences and a clinical research background in Frederick, MD. Please review the following description of the program: Provide support to the Army Medical Research and Materiel Command, Office of Research Protections (ORP) for Army and DOD funded research. Responsible for ensuring research is conducted in compliance with Federal (Department of Defense, Army, HHS, FDA) laws, regulations, policies and guidelines, and that the rights and safety of human subjects involved in the research are protected. Review and evaluate exempt, minimal risk and greater than minimal risk human research protocols, consent forms, supporting documents, study amendments, adverse event reports, and continuing review reports and advise the ORP. Protocols include investigational drugs (pharmaceuticals and biologics) and medical devices in Phase I, II and III clinical trials, multi-site, international studies and a wide variety of human research submitted by military research facilities, academia and industry. Will also provide guidance for developing protocols. Assist Institutional Review Boards (IRBs) and investigators with obtaining DoD Assurance Agreements. Participate in planning, execution, and preparation of reports for staff assistance visits designed to educate personnel, observe operations, and audit IRB and investigator study records. Develop policies and procedures relating to the protection of human subjects. Candidates selected will be subject to government security investigation. Positions are available for both mid level professionals and senior level Subject Matter Experts. DESIRED EXPERIENCE: •Minimum Bachelor's Degree in the Health Sciences •Clinical research background •Excellent oral and written communication skills •Working knowledge of MS Office •Experience with application and interpretation of regulations •U.S. Citizenship •Experience working with FDA, OHRP, or university IRB administrative office How to apply: Qualified candidates should submit resumes to bginyard@amdexcorp.com. Please indicate Job #CC002/CL on all correspondence. EOE. M/F/D/V

Baltimore - Director, Intellectual Property

Amplimmune, Inc., a start-up biotechnology company, has an opening for a Director, Intellectual Property at its facility in Baltimore, MD. The Director, Intellectual Property will be responsible for managing the company's intellectual property activities and developing patent strategies to achieve the company's business goals. Responsibilities include (i) managing the company's intellectual property estate (including overall strategic portfolio planning); (ii) developing and implementing patent filing and freedom-to-operate strategies; (iii) supporting business development initiatives and interacting with strategic partners; (iv) directing outside counsel; (v) advising senior management and the board of directors, and (vi) overseeing departmental employees and the legal budget. The position will also include negotiating, maintaining, and ensuring compliance of contracts related to business and IP matters. Must have excellent understanding of immunology, strong analytical skills, and the capability to build and maintain well organized systems. Applicants must meet the following requirements: Ph.D. in the biological sciences with a strong emphasis on immunology; 7-10 or more years of experience in managing intellectual property in the biotechnology industry; strong knowledge of U.S. and European patent law including filing and prosecuting new applications; and capable of conducting competitive analyses. The Director, Intellectual Property should maintain excellent verbal and written communication skills; be able to learn quickly; work independently; maintain computer proficiency; and interact with a proactive and result-oriented R&D team. Send resume and salary requirements to HResources@Amplimmune.com. Amplimmune, Inc. is an Equal Opportunity Employer.

Baltimore - Clinical, Regulatory and Research Jobs

Click here to apply online The specific duties of the Associate Director, Nonclinical Drug Safety Evaluation are as follows: • Responsible for reviewing, evaluating, interpreting, integrating, reporting and compiling of nonclinical toxicology, pharmacology and ADME, toxicokinetics, drug metabolism and bioanalytical data from Pharmacology, Toxicology, ADME and metabolism studies. These reviews involve review of study design and evaluation of data from safety pharmacology and pharmacology studies. . The specific duties of the Senior Manager, Clinical Drug Safety include: • Serve as medical/technical resource for Scientists, Associates and Assistants • Participate in providing training to CS&PV team members and other Otsuka staff as appropriate, on the medical aspects of programs. The specific duties assigned to the Manager Labeling & Promotion Compliance, Regulatory Affairs are as follows: • Represents regulatory affairs at review meetings. • Provides critical regulatory review and determines whether advertising, sales training materials, drug labels and labeling comply with regulations and guidelines Apply Online

Baltimore - EMT Positions

Headway Corporate Resources is currently seeking several Industrial/Construction Site EMTs for our client, a diverse engineering, construction, technology, fabrication, environmental and industrial services organization with 25,000 employees in strategic locations around the world. The Industrial/Construction Site EMT will assists with implementation of Environmental Health & Safety plans and maintains records and logs as required by EHS Department. Inspects work areas, machinery, equipment and working conditions to ensure compliance with company, state, and federal safety policies and regulations. The incumbent will also provide medical services in accordance with site specific requirements. Assists with the establishment of the medical response program and assessment of its effectiveness, and will determines the nature and extent of illness or injury and establishes priority for required emergency care. Based on assessment findings, renders emergency medical care. Works under direct supervision of EHS Manager or Site Manager Requirements for this position include: Current State/National registration as EMT-Basic Industrial experience, construction is ideal. Basic understanding of physical and biological science Specialized training and certification to meet regulatory requirements (OSHA 1910.120, 40 hour HAZWOPER, applicable 8 hour OSHA training) Must possess a current driver’s license in the State where employed except where exempt by State regulation. Current adult and child CPR certification with AED. Certification to collect drug screens is preferred This is a contract or contract-to-hire opportunity There are 3 positions currently available. One in each of the following locations. Dickerson, MD Aquasco, MD Newburg, MD For immediate and confidential consideration, please forward a current copy of your resume to dcoley@headwaycorp.com

Baltimore - QA Specialist II

Good Afternoon please read the below job description and if you are interested please contact Chris Wilkins via e-mail or phone 410-290-3262 or christopher.wilkins@adeccona.com Thanks for your time. QA Specialist II Rockville, MD Position Objective The QA Specialist is responsible for oversight of Quality System compliance issues. Essential Functions Review assay data, protocols, reports, technical specifications, RIRs Review batch records and other documents for auditing requirements Conducts facility and in-process inspections Trains other QA auditors as a Qualified Trainer Audits custom assays Reviews SOPs/other documents for compliance requirements Reviews validation protocols and reports Works with Operations Groups to implement procedures to improve data accuracy Demonstrates verifiable turnaround times Other GLP/GMP duties as assigned Nature and Scope: Takes independent ownership of specific quality system aspects. Is capable of making decisions and representing quality in cross functional settings. Is capable of cross training others in the area. May be relied upon to provide regulatory guidance in specific areas. Has regulatory knowledge in defined areas. Education: BS degree in a life science Experience: A minimum of 2 years experience in Quality Assurance in a GMP or GLP environment in a toxicology-related background. Contacts: Has contact with all levels of company employees as well as interaction company subcontractors/vendors and with customers. Working Conditions: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing this job, specifically during audits/inspections, the employee will be exposed to moving mechanical equipment, harsh and/or toxic chemicals and biologicals, low levels of radiation and extreme cold (-70C). Noise level in some areas can exceed 100 decibels. Overtime may be required. Adecco is a EOE

Baltimore - Laboratory Technician

Responsibilities •Perform bulk manufacturing, filling, labeling and packaging operations •Follow SOP’s and cGMP guidelines to ensure product specifications are met •Perform shipping and receiving activities •Perform quality control activities on raw material and manufactured products, including analyzing and interpreting results •Assist with validation related to manufacturing scale-up and automation •Assist with qualifying alternate vendors for key raw materials, including identifying vendors, determining specifications, performing laboratory experiments and analyzing results •Assist with transfer from product development to manufacturing, including writing related SOP’s •Cross-functional technical responsibilities in product development including processing patient samples and analyzing results Education •BS degree or equivalent laboratory experience Experience •Knowledge of basic laboratory equipment •Prior experience working in a cGMP laboratory •Knowledge of reagent processes, laboratory and production procedures Supervisory Responsibilities •None Work Environment: Open office environment

Baltimore - SAS Developers

Multiple openings for SAS Developers in the following areas: Clinical Data Management - experience to program edit checks and adhoc listings for data management. Create SAS data structures, upload data transfers to and from CROs. CDM System Support - Prior experiencing supporting Oracle- or SAS-based applications for the collection and management of Clinical Research data (particularly "CRF" or Case Report Form data) is a plus. Examples of such systems would include ClinTrial, Oracle-Clinical, PhaseForward's INFORM, Medidata's RAVE, etc. Clinical SAS Programming - Provide assistance and programming for the development, validation and implementation of study and project level specific SAS programs that are created within Clinical Information Science. e.g. Produce SAS reporting programs to deliver the tables, listings and graphical reports and reporting datasets required to support final clinical study reports, submission high level documents, publications, and commercial support work.Produce SAS components that will contribute to an electronic submission, including data sets, programs and content documentation to meet the demands of regulatory authorities. Marketing/Sales - Must have experience with data manipulation, IMS experience a plus, but not required, some mainframe experience, able to respond to requests, and be able to deal with data sets. SAS Programmer to maintain databases/warehouses in SAS, Oracle, DB2 and MS/Access. Will be maintaining the data libraries that support Resource Allocation Group and Promotion Response Insight. Epidemiology/Public Health - Statistical programming and data analysis requirements of the Epidemiology and Health Economics. Typical assignments include: data manipulation, data modeling, logistic regression, sampling optimization, matched analysis, propensity scores, and other statistical procedures associated with Epidemiology, Outcomes Research, and Health Economics. Must have experience with one or more of these databases: MedStat, MarketScan, Pharmetrics, Ingenix, Premier, Medicare, or Medicaid. NO THIRD PARTY CANDIDATES - Must be US citizen or US permanent resident

Baltimore - Geologist

Engineering Job Classification: Direct Hire Description:Our team of consultants deliver services internationally through our management and technical specialists and our network of associates. We provide value-added service offerings that will enhance your company's environmental program initiatives. Columbia based firm is currently looking for motivated individuals with 2 to 5 years of experience in the petroleum remediation field. Company requires:- Minimum of a Bachelors degree in Geology, Engineering or related science. - Remediation experience in Maryland, District of Columbia, Virginia and/or Delaware is a plus. - Professional registrations in Geology or Engineering are preferred. - Experience in groundwater and soil sampling, design, installation and operation and maintenance of remediation systems, geoprobe/drilling activities, monitoring/assessment reporting- Candidate should have experience with sub-contractor oversight, technical data evaluation, work plan generation and project management. - Strong organizational and communication skills This role will report to a Baltimore Area, Maryland project manager and will provide the selected candidate with opportunities for growth in their technical field of interest.CompetenciesDesired:GEOTECHNICAL, ENVIRONMENTAL ANALYSIS, ENVIRONMENTAL REMEDIATION SYSTEMS, GROUNDWATER SAMPLING Contact Information Contact: Teeters,Matthew B

Batonrouge - 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!

Batonrouge - Environmental Consultant

Natural Resource Group LLC is seeking an Environmental Consultant to join our recently established and evolving staff base in Baton Rouge as part of our Gulf Coast region operations. The specialist would assist mainly with energy-related capital development and compliance initiatives, with an emphasis on FERC-regulated pipeline and underground storage facility construction projects. However, this regulatory focus may expand beyond the immediate arena of energy-related projects to tangential industries such as chemical processing and manufacturing. The ideal candidate will possess the skills and experience necessary to work in a technical and managerial capacity on multiple concurrent projects. He/she will have the opportunity to serve as a task manager on large multi-disciplinary projects or as the overall manager on smaller projects, with the necessary oversight and support from senior regional staff. The primary responsibilities of this position include execution and management of permitting and regulatory compliance projects associated with the siting, construction, and modification of oil and gas transmission, storage, and distribution facilities, as well as a variety of industrial and chemical plants. The individual will assist with regulatory research, data collection and analysis, and the preparation and review of various technical documents or document sections (resource reports, EAs, EISs, and permit applications). A secondary focus would be assisting with the development of proposals and budget estimates for regional and national projects. The candidate would be responsible for information gathering, technical review, regulatory assessments, application development, and agency communications; attend agency/public meetings as required; prepare scope of work documents for subcontractors; review project proposals; and manage the work of subconsultants and field survey crews. This position will require client interactions and some assistance with business development and proposal preparation. Project work may involve some travel for agency meetings, project team meetings, and/or fieldwork but typically each trip would be of limited duration (one to three days) and total travel time would likely be less than 10 percent of work time. REQUIRED QUALIFICATIONS (SKILLS, EXPERIENCE, AND EDUCATION): Suitable candidates would possess a minimum of a 4-year related science or engineering degree with an emphasis on environmental coursework and four to eight years of relevant work experience. Top consideration will be given to candidates with environmental consulting experience. Ideal candidates would have a minimum of four years of permitting and regulatory compliance project experience and extensive knowledge of state and federal environmental regulations. Other assets include air permitting experience; a working knowledge of endangered species and wetland policy; natural resources management agencies; soil science; GPS technology; and map interpretation (e.g., NWI, USGS, aerial photography). A thorough working knowledge of MS Office Suite software programs is necessary. Ideal candidates would possess strong oral and written communication skills, keen orientation to detail, and recognized organizational abilities. Self-motivated, quick learning, flexible individuals who have a common-sense approach to conducting business and workload management will be most successful. Company Overview: Time and time again our clients tell us that the talent, expertise and professionalism of our consultants and support staff are second to none. We agree. That’s why the culture at Natural Resource Group LLC (NRG) prioritizes the people who make us an industry leader. NRG specializes in providing environmental and public affairs consulting services to energy clients. Since its inception in 1992, NRG has grown to become the largest group of environmental professionals solely focused on energy projects. Our 100+ person firm is headquartered in Minneapolis, with offices in Houston, Providence, Denver, Portland, Baton Rouge, and Charlotte. At NRG, we provide employees with challenging, dynamic and rewarding work in an environment that emphasizes high standards, quality deliverables, strong collaboration, opportunity for career growth, and a “no red tape” organizational structure. Our benefits package is designed to recognize and reward employees’ contributions to our company’s success. Whether it’s our state-of-the-art offices, company-paid parking or bus passes, monthly employee incentive program, flexible work schedules, top-notch yet affordable healthcare plan, or ice cream on a hot summer day (compliments of the CEO), NRG’s employees are recognized for their hard work. If you have a reputation for delivering high-caliber, strategic results in a client-focused, fast-paced consulting environment, please visit www.NRG-LLC.com for further information on our company. Relevant Dates Pertaining to this Posting: We are actively recruiting to fill this position as soon as possible. This posting is valid for 45 days from the date of posting. Company Web Site Address: www.NRG-LLC.com Preferred Method of Application: Please submit cover letter and resume electronically to careers@NRG-LLC.com, or via the employment opportunities page on our company’s web site at www.NRG-LLC.com. Additional Methods of Application: U.S. Mail: Attn: Careers@NRG Natural Resource Group, Inc. 1000 IDS Center 80 S. Eighth Street Minneapolis, MN 55402 Facsimile: Attn: Careers@NRG (612) 347-6780

Batonrouge - Laboratory Assistant

Part-time dependable person for Laboratory Assistant. Some weekends and one holiday a year required. Hours:9am - 1pm. No experiance required, all training provided. Smoke free workplace. Culturing, cleaning, and lab analysis. Send resume' or letter of interest or stop by: A & E Testing 1602 Fountain Baton Rouge, LA 70810 Fax 767-0533

Batonrouge - Wildlife Biologist

JOB DESCRIPTION: Coastal Environments, Inc. is searching for a self-motivated person to conduct field investigations in various areas of the southeastern US. Job requirements would include wetland delineations, wetland restoration and management; mitigation; environmental monitoring; wildlife habitat evaluations; wildlife and land management advisory services. QUALIFICATIONS: B.S. in wildlife biology, biology, ecology, forestry or related fields. An additional 1-2 years experience preferred, but not required. Applicants should be knowledgeable in biological sciences with emphasis on wetland delineations; wetlands habitat resource restoration and management; biological evaluations and assessments; proposal and report writing. RECOMMENDED SKILLS: Wetland management techniques; knowledge of fauna and flora of Gulf Coast Region; study design / sampling methodology / statistical analysis / report preparation; assessment of wetlands, habitat values, and functions; strong oral and written communication skills; computer skills; ability to use boats, airboats, ATV; ability to work well with clients and colleagues; NEPA compliance documents and permitting, complete tasks on time and within budget. SUBMIT RESUME TO:Coastal Environments, Inc. Human Resources 1260 Main Street Baton Rouge, LA 70802 (225) 383-7455 (Fax) rgreig@coastalenv.com

Bellingham - Resource Management Specialist

COMPANY: Stimson Lumber Co JOB TITLE: Resource Management Specialist REPORTS TO: Inventory & GIS Manager DIVISION: Inland Operations LOCATIION: Newport, WA CONTACT: Sean McLain - HR - 503-357-2131 xt 4285 (please also submit a resume before you call) General Summary: Assist in all aspects of the Inventory & GIS Manager’s responsibilities and duties, coordinate the analysis of Stimson’s interest in external issues and groups, where inventory & GIS skills are used. Coordinate the Inland Region contract nursery and tree planting efforts. Essential Duties and Responsibilities: 1. Assists in the forest inventory and GIS update efforts; overseeing forest inventory contracts approximately 60% of time 2. Assist State Managers in representing Stimson Lumber Company where special silvicultural, inventory & GIS analysis is needed in interactions with selected external groups and organizations in dealing with evolving science and regulatory issues affecting forest management activities such as wildlife, fisheries, air and water quality, special habitat management plans, and land use planning; approximately 10% of time. 3. Assist State Fee Land Managers with coordination of Inland Region reforestation efforts which involves maintaining seed inventory, nursery contracts, tree planting program; pre-commercial thinning and stand maintenance contract activities; approximately 25% of time. 4. Coordinate Newport office safety committee and program, liaison with other Resources safety efforts; approximately 5% of time. Required Knowledge, Skills, and Abilities: 1. Knowledge of Inland forest silvicultural practices, operational costs, log markets, pesticide use and application, and ability to operate within stringent and complex forest practices regulation arena. 2. Skills in oral and written communications, use of forest inventory data bases, spread sheets, geographic information systems, and ability to work effectively with external contacts and contractors. 3. Ability to operate with minimal supervision. 4. Some limited travel within Inland Region required. Education and Experience: This position requires a degree in resource management, preferably a four year degree with a major in one of the forestry disciplines; and, at least 5 years of field experience in forestland management, including supervisory and operational responsibilities.

Bellingham - Field Project Implementation Manager - Municipal Wastewater & Water

****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 & 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 -Principals only. Recruiters, please don't contact this job poster. -Please, no phone calls about this job. -Please do not contact job poster about other services, products or commercial interests. Location: Seattle Compensation: $50k - $75+k/year, DOE - Outstanding Benefits! Beautiful Waterfront Offices! Principals only. Recruiters, please don't contact this job poster. Please, no phone calls about this job! Please do not contact job poster about other services, products or commercial interests.

Bellingham - Biodiesel/veg person needed

We are a growing business in need of a good veg oil or biodiesel person. Handsome pay and stock options available if you fit the mold. 5094994508---Doug

Bellingham - 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.

Bend - GIS Analyst

Are you passionate about earth science and technology? Are you driven by a strong desire to work on exciting projects and provide world-class service to clients? Does joining the team of a true industry leader sound like the professional challenge you are seeking? If so, GeoEngineers, Inc. is looking for you! GeoEngineers, a leading national earth science and technology consulting firm recently voted Eastside Business of the Year by the Bellevue, WA Chamber of Commerce, is seeking a talented GIS Analyst. This position can be located at any of our 16 office locations. The GIS Analyst will perform professional work involved in the production, distribution, data collection and application support of GeoEngineers' GIS system. Responsibilities will include providing technical support in the creation and maintenance of GIS data and cartographic products and the completion of map requests in a timely manner. Some travel may be required. With hundreds of experts working from 16 locations nationwide on domestic as well as international projects, GeoEngineers provides global service with a local presence. We offer the resources of a large firm with the feel of a small one. We are known for applying fresh, creative thinking to meeting our clients' objectives. Our strength lies not just in our expertise, but in the way we are able to apply this deep knowledge to discover innovative solutions to the challenges at hand. GeoEngineers offers a unique environment that fosters individual growth and development, promotes teamwork and rewards performance. You'll be working in a dynamic, high-energy setting as part of an award-winning team with a strong, successful track record. Our employees are our most valuable asset. Our competitive salary and benefits package exceeds industry standards and includes: Medical/Dental/Vision/Life insurance 401(k) with matching contribution Profit sharing and merit-based bonus plans Paid holidays, vacation and sick leave Wellness programs Relocation assistance Professional development This is an exciting opportunity to work in a challenging and dynamic environment for a growing company! For immediate consideration, apply online at http://www.cytiva.com/cejobs/templateGeoen.asp. To learn more about life at GeoEngineers, visit http://www.geoengineers.com/ EOE Requirements: Preferred Qualifications: BA/BS in Earth Science, Geography or related field. One year of experience with GIS mapping or applied use of GIS technology. Proficiency with ArcGIS Desktop applications and preferred experience with ArcInfo, Spatial Analyst and MS Access and/or MS SQL databases. Broad skill set in geospatial manipulation, geospatial data processing and mapping. Experience with cartography and map production in a professional environment. Proven orientation for detail and quality. Ability to prioritize multiple tasks and solve problems in a dynamic work environment. Ability to work independently as well as within a team environment. Professional level language skills in verbal communication and written correspondence and ability to effectively convey technical information to non-technical personnel. Ability to travel as needed.

Bend - District Fish Biologist

District Fish Biologist Oregon Department of Fish and Wildlife Bend, OR Searching for a skilled individual to contribute valuable biological work as the District Fish Biologist in Bend. Plan, direct and coordinate management of specific aspects of fish resources and supervise employees in the day-to-day field activities of gathering data pertaining to specific aspects of fish resources. Responsible for collecting and summarizing data on harvest, spawning, escapement and distribution of various fish species within the district; protecting aquatic and riparian habitat within the district by frequent field investigations of land and resource use operations and recommending to various regulating agencies and private landowners actions to avoid, minimize, or mitigate damage to the fish resource; identifying and developing habitat improvement and public access projects; providing information to civic groups recreational organizations, governmental groups, and the general public regarding the department’s total fish and wildlife programs, activities and related topics. For more information, see recruiting announcement at www.dfw.state.or.us/hr Qualifications: Requires three years of biological experience in a fisheries or wildlife program. At least one year of the experience must be at the professional level, performing research activities such as planning and conducting investigations, analyzing data, applying pertinent laws and regulations, and coordinating and monitoring project activities; AND a Bachelor’s degree in Fisheries or Wildlife Science or a closely-related Bachelor’s degree with at least 45 quarter (30 semester) hours of biological/ecological coursework; or three years of biological experience performing studies or research in a fisheries or wildlife program. One year of experience must have included lead work or supervisory duties. A Master’s degree in Fisheries or Wildlife Science, or a closely-related Master’s degree in biological/ecological sciences will substitute for up to one year of required experience and a Doctorate in Fisheries or Wildlife Science, or a closely-related Doctorate in biological/ecological sciences will substitute for up to two years of required experience. Preference will be given to applicants with salmon, steelhead, trout and warm water fish experience, as well as public involvement and conservation planning. Closing Date: November 15, 2007 Contact: For application materials visit ODFW’s Web site at: www.dfw.state.or.us/hr or call ODFW’s jobline at (503) 947-6052.

Bend - 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.

Binghamton - 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!

Binghamton - Chemistry Lab Assistant Needed

Novomer is an Ithaca, New York based specialty chemicals and materials company. We have an immediate need to add a part time Lab Assistant to our team. The Lab Assistant will help Novomer's team of scientists and engineers in scaling up the production of an innovative class of renewable polymers. The work will entail preparing, monitoring and cleaning laboratory equipment; shipping and receiving of lab supplies and chemicals; storage and inventory of equipment, chemicals and supplies; and general support tasks as required. A successful candidate will be reliable, self-motivated, willing to follow procedures effectively and able to work as part of a team in a dynamic fast growing company. Must be able to lift 40 pounds. Opportunity is for 20 hours / week to be scheduled during work hours (weekdays 8am - 5pm). Competitive hourly pay. Experience working in a lab environment preferred but not required. Current college students (especially in Chemistry and Chemical Engineering) encouraged to apply. To apply, forward your resume and references to jobs@novomer.com For mor information about Novomer, visit us on the web at www.novomer.com

Binghamton - Chemistry Research Technician Needed

Novomer is an Ithaca, New York based specialty chemicals and materials company currently scaling up the production of an innovative new class of renewable polymers. We are currently are seeking a part time/full time Research Technician. The Research Technician will be responsible for researching new materials for applications in a number of industries. The Research Technician will also help develop new materials, determine new markets and support business, quality and technical service strategies. The candidate must have a degree in chemistry and preferably a higher degree in Polymer Science or Materials Science. A minimum of 5 years experience in materials science is required and experience with applications or product development is highly desired. A successful candidate will be creative, self-motivated, able to work as part of a team in a dynamic fast growing company and have strong written and verbal communication skills. To apply, forward a CV with three references to jobs@novomer.com. For more information about Novomer, visit us on the web at www.novomer.com

Binghamton - 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.

Bham - Environmental Scientist/Engineer

Anchor Environmental, a national environmental and engineering consulting firm is seeking a full-time ENVIRONMENTAL SCIENTIST or ENGINEER for its Gulf Coast office, located in Ocean Springs, MS. The primary focus of this position involves providing technical support in the assessment and remedial planning of contaminated sediment sites along the Gulf Coast and other areas of the United States. Responsibilities may include, but are not limited to, supporting the development and implementation of work plans, environmental data analysis and management, site investigations, report preparation, administrative support and equipment maintenance and organization. Some travel will be required. This position is well suited for a recent Masters-level graduate in Environmental Sciences or Engineering with 1-3 years experience working in an environmental consulting firm. A winning candidate will have a strong background in biology, geology, hydrology, risk assessment and/or environmental engineering as well as database and GIS experience. The position requires excellent written and verbal communication skills and the ability to work independently in a team context. Anchor Environmental offers excellent benefits including employer-sponsored health care, 401(k) + match, and an Incentive Pay Program. Qualified applicants please email your resume and salary requirements to careers@anchorenv.com with Gulf Coast Environmental Scientist in the subject heading. We are an Equal Employment Opportunity Employer

Bham - 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.

Bham - Production Supervisor

JOB TITLE:Clinical Production Supervisor 2nd shift FLSA STATUS:Exempt REPORTS TO:Shift Production Manager PRIMARY FUNCTION: Responsible for training, monitoring and supervising clinical production staff. Responsible for employee assignments, safety, quality, production rates, material reconciliation, production reports, timelines and union policies. Department assignments cover blister card packaging, over-encapsulation, bottle filling, pouching operations, clinical labeling, kit assembly, collating and distribution. Responsible for maintaining Class 100,000 clean rooms and controlled substances II through V. SPECIFIC DUTIES, ACTIVITIES, AND RESPONSIBILITIES: •Monitors, organizes and performs all functions associated with packaging of clinical trial supplies and assures compliance to GMPs, SOPs, FDA, DEA and OSHA rules and regulations. •Implements procedures to increase productivity and decrease downtime. •Works closely with Clinical Coordinators to establish production needs and requirements for ongoing and future studies. •Oversees both primary and secondary areas equipped with various pharmaceutical packaging equipment including automated bottle line, form, fill and seal, card sealing, labeling and patient kit assembly. •Employee performance evaluations, new employee hiring, disciplinary notices, employee termination, according to company guidelines and performance requirements as established in the union contact. •Develops, reviews and edits related production SOP’s (operational, maintenance, cleaning). •Responsible for maintaining and ordering personnel, safety, disposable and support packaging supplies. •Review and approval of production staff vacation and personal days, along with leave of absence requests. •Responsible for completing batch records in a timely manner. •Investigate and prepare out of specification reports related to production. •Security, accountability and reconciliation of controlled substance in clinical production. •Staging, reconciliation and inventory label generation in JD Edwards. POSITION REQUIREMENTS: •Clinical Trials Supplies experience preferred •Computer literate (Microsoft Word) •Pharmaceutical Packaging and Manufacturing experience •JD Edwards experience or similar ERP systems •Working knowledge of cGMPs, DEA and OSHA rules and regulations •Leadership and team building skills •Demonstrate ability to train, motivate, direct and supervise production personnel •Knowledge of packaging equipment in a Just-in-Time environment •Proven ability to develop Standard Operating Procedures REPORTS TO: Manager of Clinical Operations & Production Manager SUPERVISES: •Hourly Production Personnel EDUCATION: •Bachelor of Science Degree in Health/Chemistry/Pharmacy related field EXPERIENCE OR EQUIVALENT: •5+ years Clinical, contract or production experience

Bham - Regional Clinical Research Associate I/II:

This is a home based regional Clinical Research Associate position. For this position you must have been with a pharmaceutical/Clinical Research Organization for at least six months. This must have clinical research associate experience. You must have independent monitoring experience. I will consider any therapeutic area. You must be within an hour of a major airport.

Bham - Mortgage Consultant

A successful business is dependent on the quality of the individuals that collectively contribute to serve its clients - our company embraces that fact to the fullest extent. Our expansion plans call for expanding into new markets and expanding in markets we already serve, based on finding individuals who embrace our philosophies. A significant part of the rewards of succeeding with our firm is that we offer one of the industries most lucrative benefit plans. We continuously ensure that the benefits we offer remains competitive with leaders in our industry. This results in programs that deliver the best combination of quality, choice, and value to our employees. Come be a leader. We have one goal and that’s to be the best mortgage company in our area. In order to achieve that goal, we have established commitments to our clients, employees and the communities in which we do business. In order to achieve this goal, our employees are committed to creating an open, entrepreneurial and dynamic workplace that is built on a meritocracy and allows each employee to contribute to the best of his or her ability. If you want a career with a company where employees can be Leaders, work in an environment that encourages openness and honesty, cares about the local community and sets high standards, we are the place for you. We offer a wide range of programs and services to help our employees improve their skills, grow in their career, and meet their commitments to both their personal lives and their careers. We support the inclusion of all employees and we embrace those characteristics that make each of us who we are. Our reasoning is simple: we believe we can be a workplace considered by all colleagues as an excellent career choice and a great place to work. Email us your cover letter and resume. Our employees must possess: • Full understanding of the retail mortgage industry. • Mastery of the English language. • Minimum of two years college education. • Minimum of one year loan origination experience. • The ability to solve problems with extraordinary time management skills.

Bham - Laboratory Supplies & Chemical Sales

Laboratory Sales Representative Expand your professional options. Build your own client base. We are looking for experienced scientific and chemical sales professionals who know the meaning of relationship sales and believe in taking care of customers. Do you call on labs, research, QC/QA, manufacturing or clinical labs? Are you limited to what you can sell and make? This is a well paying commission opportunity allowing the right person a part time or a full time option. No cap on the income you can earn. We are distributor of laboratory supplies, consumables and chemicals providing reps the flexibility of managing their business. If you understand this market and know how to convert competitive products, this can be a great opportunity for you. Requirements: BS Degree: chemistry, bio-related or equivalent Understanding market and customer needs Maintain updated knowledge of the industry and competitor’s products Prepare sales contract, contracts, quotes, prices and terms Four plus years sales experience Computer skills: Web, excel & word Independent Organized Responsible Dependable Demonstrate growth and profitability Simple formula for success: Build the business profitably and ethically Do not waste selling time with management reports, weekly plans or useless busy-reports The customer is number one! This is a commission only opportunity. Email: labrep@yahoo.com

Bham - Sr. Food Scientist - Product Development

POSITION:Product Development Scientist DEPARTMENT:Research & Development POSITION SUMMARY: This position is to conceptualize, develop, drive and implement product & process innovations that deliver new and exciting opportunities. Specifically, this role will be responsible for identifying and executing novel food products and technologies that meet consumers’ needs. JOB RESPONSIBILITIES: Responsibilities include: 1)Hands on new product and process development including laboratory, kitchen and pilot plant investigations. 2)Identify evolving food technologies through publications, conferences and networking. 3)Apply engineering and scientific methodologies to the development processes. 4)Working within a multi-disciplinary team to create breakthrough innovations. Work with the franchise groups to understand consumer needs and champion product innovations that can meet these. 5)Optimize existing platform technologies, identify and develop novel technologies to provide future competitive advantage. 6)Actively participate on the project technical team meetings representing the interests of product/process development. Additionally, share pertinent information from these meetings through presentations to R&D. 7)Develop new product/process ideas, champion and communicate these ideas through prototype development, PowerPoint presentations and/or posters. 8)Delivery of IP for technical insulation of new technology QUALIFICATIONS/EDUCATION AND EXPERIENCE: •B.S. degree in Food/Chemical Engineering, Food Science/Technology or related discipline and minimum 3 years of relevant experience required. Additional post graduate qualifications preferred. •Experience in new product/process development would be advantageous. •Knowledge of ‘state of the art’ food science and technologies required. •Experience in extrusion, thermal processing and/or shelf stable preservation technologies preferred. •Good experimental skills and a familiarity with experimental design and statistical data analysis. •Creative with excellent problem solving skills •Ability to communicate scientific principles clearly and precisely. •Good communication skills and ability to work in cross-functional teams required. •Self-starter with assertive project ownership qualities is essential •Preferred knowledge of food and raw materials safety and quality assurance techniques. •Willing to travel up to 30% of time

Bham - Researcher

The individual will join a multi-disciplinary team of scientists, focused on the development of novel therapies and biomarkers relevant to Alzheimer’s disease (AD). The position is within a new research group that is studying synaptic physiology and pathology in AD. The individual will contribute to the project goals using electrophysiology of primary neurons, molecular biology techniques and/or microscopic imaging. Qualifications Requirements include a bachelors or masters degree in a relevant biological field. Experience in brain slice physiology is desireable.. Additional experience with protein biochemistry and cell culture is desirable. A high level of competency in data analysis and presentation is required. Good verbal and written communication skills and the ability to work effectively in a matrix organization are essential. For more information, review the job at: http://www.bioemployment.com

Bham - Associate Scientist

We are a growing company in a fast-paced environment and currently seek an Associate Scientist, Analytical Development to join our team. Duties and responsibilities will include assisting in the introduction and transfer in-house of new analytical methods to support process development, quality control and manufacturing operations through routine testing. Assists with writing procedures and test methods and their transfer to quality control. Additionally, assists with maintenance of analytical and production equipment. Requirements . Qualifications: The qualified candidate requires a Bachelors/Master’s degree in chemistry, biochemistry, biology, or related engineering discipline or equivalent with a minimum of 0 to 2 years relevant experience. For more details on this job and others visit: http://www.bioemployment.com

Blacksburg - 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!

Blacksburg - Human Subject Protection Scientists

AMDEX Corporation is seeking professionals with a minimum of a Bachelor's Degree in the Health Sciences and a clinical research background in Frederick, MD. Please review the following description of the program: Provide support to the Army Medical Research and Materiel Command, Office of Research Protections (ORP) for Army and DOD funded research. Responsible for ensuring research is conducted in compliance with Federal (Department of Defense, Army, HHS, FDA) laws, regulations, policies and guidelines, and that the rights and safety of human subjects involved in the research are protected. Review and evaluate exempt, minimal risk and greater than minimal risk human research protocols, consent forms, supporting documents, study amendments, adverse event reports, and continuing review reports and advise the ORP. Protocols include investigational drugs (pharmaceuticals and biologics) and medical devices in Phase I, II and III clinical trials, multi-site, international studies and a wide variety of human research submitted by military research facilities, academia and industry. Will also provide guidance for developing protocols. Assist Institutional Review Boards (IRBs) and investigators with obtaining DoD Assurance Agreements. Participate in planning, execution, and preparation of reports for staff assistance visits designed to educate personnel, observe operations, and audit IRB and investigator study records. Develop policies and procedures relating to the protection of human subjects. Candidates selected will be subject to government security investigation. Positions are available for both mid level professionals and senior level Subject Matter Experts. DESIRED EXPERIENCE: •Minimum Bachelor's Degree in the Health Sciences •Clinical research background •Excellent oral and written communication skills •Working knowledge of MS Office •Experience with application and interpretation of regulations •U.S. Citizenship •Experience working with FDA, OHRP, or university IRB administrative office How to apply: Qualified candidates should submit resumes to bginyard@amdexcorp.com. Please indicate Job #CC002/CL on all correspondence. EOE. M/F/D/V

Blacksburg - Program Manager, Reimbursement

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. Job Description - External: The primary day-to-day client contact for existing projects. Oversee staff activities and performance. Provide management, administration and leadership to ensure that projects proceed on time and within designated budget. Responsibilities: ' Supervise Staff ' Provide leadership, coaching, mentoring, feedback and role modeling to team members to assure quality, accuracy and completeness of deliverables ' Communicate to team members the scope of work, timelines and program/project goals, technical information, deliverables, and input from client throughout the duration of the program/project ' Inform team members of any new information or modification of program/project related issues that may affect specific responsibilities of team members ' Schedule activities and deliverables, including timelines, for staff ' Facilitate communication within the team through team meetings, e-mails and monitor engagement/morale of team members. ' Provide or arrange for program/project-related training as needed for team members ' Resource planning and management. Track resources and actual time spent for project tasks for all team members ' Adhere to program SOPs and metrics ' Serve as primary client contact for day-to-day program activity ' Respond to day-to-day client inquiries associated with specific programs/projects ' Manage client expectations ' Prepare and provide activity reports for the client ' Coordinate operational activities of program/project from initiation to completion ' Write program SOPs, guidelines, client deliverables (e.g. reports, memos, etc.) ' Ensure that appropriate review and approval of project-related documents and correspondence occurs ' Understand billing and coding procedures for program products ' Assure appropriate monthly revenue is recognized for all assigned projects ' Submit monthly resource/activity reports to Associate Director/Director ' Calculate monthly revenues recognized for the program/project and submit monthly updated forecasts for revenue recognition and invoicing to the Associate Director ' Assume responsibility for all tasks which are not otherwise delegated ' Conduct performance reviews ' Understand reimbursement and patient assistance strategy and program design for pharmaceutical products ' Identify new opportunities within client account and collaborates with Associate Directors ' Support organization vision and values and ensures team activities are aligned accordingly ' Prepare and conduct client presentations/trainings as necessary ' Travel as required ' Perform other tasks as assigned by management Experience - External: Education: Bachelor's degree Minimum Work Experience Requirements: Minimum of 3 - 5 years in health-related field with minimum 2 years of managing people and projects. Special Skills/Knowledge: Moderate level consulting skills. Thorough working knowledge of organization's service offerings and processes. Keeps current on body of knowledge within area of responsibility. Understanding of the pharmaceutical, biotechnology, medical device or other healthcare industries. Demonstrated leadership skills that include the ability to gain trust and confidence with a variety of personnel and clients. Strong interpersonal and negotiation skills; excellent decision-making skills and strong analytical skills; must be well organized and show attention to detail; must understand complex organizational relationships; take a proactive approach in dealing with project problems/issues; strong oral and written communication skills; strong computer skills. excellent customer service skills; travel as necessary; presentation skills, motivated to work consistently in a fast-paced and rapidly changing environment. Please Contact: Dorothy Hughes Dorothy.Hughes@kenexa.com

Bn - Clinical Trial Manager

Primary Objective of Position: Plans and manages clinical development trials. Oversees internal and external staff for the timely and quality implementation of trials. Oversees the activities of CROs. Coordinates the training of clinical and other staff. Prepares reports on clinical trials. Performs performance appraisals on direct reports. Major Duties and Responsibilities: - Prepares clinical protocols and amendments. - Oversees or performs feasibility assessment for new clinical protocols. - Identifies, recruits and approves clinical investigators. - Ensures compliance with policies and procedures. - Approves sample, investigator-prepared and IRB-approved informed consents. - Approves or write monitoring plans. - Approves the design, format and content of CRFs, study guides and subject instructions. - Oversees activities associated with clinical site start-up and ensure the collection and maintenance of essential documents. - Ensures appropriateness of forecast for investigational product. - Coordinates the preparation of study budgets. - Manages Investigator Meetings. - Manages the overall Investigational product accountability and reconciliation process. - Ensures that that CRF data queries are resolved. - Oversees and monitors work done by CROs, central labs and other vendors chosen for clinical development activities ensuring delivery against contract. - Provides study-specific outsourcing specifications for RFPs. - Ensures training of clinical staff. - Develops and administer study and project budgets. - Resolves patient eligibility and protocol deviation issues. - Assists in preparation Clinical Study Reports, Annual IND safety reports and clinical. - May monitor clinical sites for adherence to protocol and GCP. Minimum Job Qualification: BA/BS in biological sciences or related fields or BSN. Typically 7-8 years related experience in life sciences or medically related field, including 6 years of clinical development experience and previous 1-2 years of management experience. Skills and Abilities: - Knowledge of relevant therapeutic or product area - Ability to use scientific and clinical knowledge to conceptualize study designs. - Ability to evaluate scientific and clinical strategies for clinical development in a specified product area. - Detailed knowledge of regulations and guidelines ' - Ability to anticipate and resolve problems. - Ability to write and present clearly especially on scientific and clinical issues ' - Ability to work effectively in a team/matrix environment. - Excellent interpersonal, organizational, supervisory and project planning skills. - Proficiency in the preparation and review of clinical sections of study reports and BLA/NDA. - Demonstrated professional collaboration skills. - Experience in all phases of drug development, including international trials. *** Please state hourly wage requirements***

Boise - GPS SURVEYING TECHNICIAN

We pay a fixed rate per approved location and routes with bonuses and additional income oppourtunities. GPS knowledge very helpful, as well as an economical vehicle and good communications skills a must.