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Akroncanton - 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!

Akroncanton - I&I Sales Account Manager

I&I Sales Account ManagerDon’t let the title fool you, this position has substantial growth potential!Ropella and Associates, the world’s largest Executive Search Firm exclusively serving the Chemical and Allied Industries, has been retained to fill an I&I Sales Account Manager role with huge growth potential. If you know anyone who might be a possible fit, please let me know. Overview: Opportunity for international “overseas based” assignments Position is with a Global Leader in Personal Care and HI&I chemicals Work with a company on the forefront of the “Green” Movement Develop the road map and guide the company into the future with I&I Chemicals Highly visible position with huge potential to carve out your own place within the company Requirements:A Bachelor’s Degree (Chemistry preferred), MBA a plus Minimum of 3-5 years experience selling specialty chemicals for the Hard Surface cleaning and Clean in Place market Management experience a plus Entrepreneurial and a Pioneer attitude Anyone interested in the position can get a complete Position Description by contacting me.We are also working on several other positions and have identified some of the chemical industries top producers and performers. If there are needs in your organization or you would like to discuss your career, please email Robin Klempa at Klempa@ropella.com. It’s Time To PutROPELLA & ASSOCIATES To Work For You

Akroncanton - Laboratory Supply & 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

Akroncanton - All Science Majors and Recent Grads

Don’t miss the chance to meet and interview with over 150 employers at the WestPACS Job and Internship Fair. Come with your resume and professional attire on November 8, 2007 at the Pittsburgh Expo Mart, Monroeville, PA. There are real opportunities for biology, chemistry, physics and other science majors in full and part time jobs and internships. Visit www.westpacs.org for more information and entrance requirements.

Anchorage - Environmental remediation engineer

Environmental/Remediation engineer for remedial investigation / feasibility study (RI/FS), remedial technology evaluation, pilot and bench testing oversight, remediation system design, remediation system review and evaluation, site investigation, environmental assessment, and permitting projects. Duties include hands on technical project work and support, preparation of planning documents and reports, project / task management. Ideal candidate will have remediation experience to abate petroleum contamination in soil and groundwater at sites located in cold climate environments. Candidate should also possess a solid understanding of arctic engineering principles. Candidate must have good communication skills (verbal & written). Candidate must have first hand knowledge and experience with applicable Federal and state of Alaska environmental regulations. Position requires travel, field work, work in remote Alaska locations (~25% of time), and a valid drivers license. Engineering degree required (BS or MS), with 3 to 5 years experience. We offer a very competitive package of salary and benefits to the right candidate. Learn more about OASIS Environmental and submit your resume through our website at http://www.oasisenviro.com/ .

Anchorage - Biologist / Ecologist

Biologist/Ecologist to oversee and manage projects, conduct field data sampling, conduct literature searches and prepare technical summary reports for various environmental assessment projects. In addition to the technical aspects of the position, duties include project management, proposal development, coordination and communication with client and regulatory personnel. Must be able to work independently or as part of a team in remote Alaska conditions and locations. Candidates should have good work ethics, a willingness to learn and pay attention to details. Position requires 20 - 30% field work at remote sites. We offer a very competitive package of salary and benefits for the right person. Learn more about us and submit your resume through the OASIS Environmental website at http://www.oasisenviro.com/ .

Anchorage - Environmental Technician

Environmental Technician for groundwater monitoring, environmental assessment, and remediation projects within Alaska. Duties include soil, water, air, and waste sampling; groundwater monitoring; remediation system operation and maintenance; logistical support; documentation of field activities; summarize and evaluate data collected in the field; and provide support in preparation of technical reports. Work to be conducted in accordance with approved work plans and site safety and health plans. Position requires field work at remote sites (20% - 40% of time) and a valid drivers license. We offer a very competitive package of salary and benefits for the right person. Learn more about us and submit your resume through the OASIS Environmental website at http://www.oasisenviro.com/ .

Anchorage - Air Monitoring Project Manager

Hoefler Consulting Group is an Anchorage-based, Native-owned consulting firm specializing in comprehensive environmental permitting and compliance services for Alaskan industry. Hoefler provides technical services supporting the construction and operation of facilities in Alaska's unique physical, regulatory, and political environment. The firm is certified as an 8(a) BD firm by the U.S. Small Business Administration. Founded in 1995, the firm currently employs over 55 engineers, scientists, technicians, and support staff. We are seeking a Project Manager for ambient air and remote meteorological monitoring projects. Qualified candidates should have at least 5 years ambient air monitoring experience and a degree in engineering, meteorology, or equivalent background. Extensive knowledge of EPA air monitoring regulations and methods is required. Direct experience with NOX, SO2, CO, and O3 gas analyzers is required. Experience with PM2.5 monitoring, dispersion modeling, air permitting, or source testing would be a plus. Periodic travel and field assignments are required. Applicants should be able to work independently as well as on teams, and should possess good writing and organization skills. This position is based in Anchorage, Alaska. We offer a great work environment, an aggressive compensation package, and a signing bonus for qualified candidates. Resumes to: administrator@hoeflernet.com Hoefler Consulting Group is an equal opportunity employer. www.hoeflernet.com

Anchorage - Environmental Field Technician

oefler Consulting Group is an Anchorage-based, Native-owned consulting firm specializing in comprehensive environmental permitting and compliance services for Alaskan industry. Hoefler provides technical services supporting the construction and operation of facilities in Alaska's unique physical, regulatory, and political environment. The firm is certified as an 8(a) BD firm by the U.S. Small Business Administration. Founded in 1995, the firm currently employs over 55 engineers, scientists, technicians, and support staff. We are seeking an Environmental Field Technician to install, calibrate, and maintain ambient air and meteorological monitoring stations throughout Alaska. The field technician will be responsible for the operation and maintenance of sites with air monitoring equipment and/or meteorological monitoring equipment. A proven ability to test, troubleshoot, and repair electrical and mechanical systems is required. Knowledge of data acquisition systems, remote telemetry communications, and air sampling systems is desired. This position will include analysis of collected data, reporting ambient air quality and meteorological data, as well as developing monitoring quality assurance plans. A degree in environmental science or engineering, or completion of an accredited instrumentation program, plus 1-5 years field experience is desired. Candidates with direct experience in ambient air monitoring systems or CEMS are encouraged to apply. In addition to the above, applicants should be able to work independently as well as on teams, and should possess strong writing and organization skills. For this position, we desire experience in conducting monitoring programs for EPA’s Prevention of Significant Deterioration (PSD) program or other EPA ambient air monitoring networks. This position is based in Anchorage, Alaska, and will require extensive travel throughout the state. We offer a great work environment, an aggressive compensation package, and a signing bonus to qualified candidates. Resumes to: administrator@hoeflernet.com Hoefler Consulting Group is an equal opportunity employer. www.hoeflernet.com

Anchorage - Microscope analyst

PLM analyst position for environmental lab. Experience required. B.S. degree required. May require travel.

Anchorage - Need a seed collection from Healy, Ak - 50 dollars for your trouble

I'm a graduate student who needs a seed collection from the gravel bar directly adjacent to the power plant in Healy. If anyone has an hour and is driving the Parks Highway in the next two weeks, I'd love to send you a fifty dollar check to cover your time and trouble. Please email James at the CL add below.

Anchorage - 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.

Albany - 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

Albany - Senior Laboratory Technician or Assistant Research Scientist

Health Research, Inc., a not-for-profit corp, is seeking a Senior Laboratory Technician or Assistant Research Scientist (1 position) to work within a molecular clinical diagnostics team performing complex, molecular detection of viruses. Duties include accessioning of lab specimens, performance of manual & automated nucleic acid extraction methods, conventional and real-time PCR analysis and data analysis. The candidate will be involved in developing & validating diagnostic assays & research projects that will help in identification of emerging pathogens. These duties will be performed using established molecular protocols & following a unidirectional clinical workflow. Minimum Qualifications: Candidates must possess a Clinical Laboratory Technology Practitioner License & Current Registration or Limited Permit. For the Sr. Lab Tech, must have a BA/BS in Microbiology or a related field; OR an A.A.S. degree in an appropriate field & 2 years of experience performing tests & procedures in a lab or clinical setting. For the Asst Research Scientist, must have a BA/BS in Microbiology or a related field plus 1 yr of experience in that field. 30 graduate hours leading to an advanced degree in an appropriate field may be substituted for the required experience. Preferred Qualifications: Training &/or experience in nucleic acid amplification technology. Familiarity with molecular biology & virology, as well as handling of human clinical specimens at biosafety level 2 containment. Some knowledge or experience with computers, including spreadsheets & databases. Please use code W677CL when responding. Resume can be e-mailed to: HRI-mailin@healthresearch.org with a subject line W677CL or mailed to Health Research, Inc., One University Place, Rensselaer, NY 12144-3447 (applicants must include a return address and the reference code W677CL on the outer envelope). No phone calls or faxes accepted www.healthresearch.org/jobs AA/EOE/M/W/D/V

Albany - Environmental Scientist

Environmental Scientists The Tyree Organization, a leading environmental / construction firm, is seeking an experienced Environmental Scientist for our Latham, NY office. Requirements: At least 2+ year’s experience in site assessment and subsurface investigations required. BS in Environmental Science, Geology or a related field a must. We offer opportunity for growth, a full benefits package, and a competitive salary. For immediate consideration, please fax, mail or email your resume to: Contact Information: E-mail resume to Dvitucci@tyreeorg.com or fax to 631-249-5867 Phone: 631-249-3150 ext.222

Albany - Biometrics Reseller Seeks Experienced Sales/Software Manager

Biometrics reseller start-up is seeking a dedicated, and experienced manager for partnership development and for technological assistance. The successful applicant will have the following qualifications: - Four year college degree; MBA or graduate degree preferred (company is run by law students!) - At least 1+ years of experience in either the sale or programming of biometric related products, preferably experience with access security, payment processing systems or other related consumer biometric products. - Strong communication skills - Willing and excited about working in a fun, flexible and honest environment where ideas, innovation, and incentive are HIGHLY VALUED. - Someone who is truly interested in building a strong reselling entity from to p to bottom. Duties: - Development of reseller relationship - Creation and development of initial sales force - Primary contact point for technical issues during contract and program related negotiations. Much more to this job. Please contact us for more information. Please send resume (cover letter not necessary), along with salary requirements to the above listed e-mail address provided by Craigslist. Thank you.

Albany - 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!

Albany - Project Manager

Our Lower Hudson Valley area office in Patterson, New York has an opening for a Project Manager. Responsibilities and Duties: -Oversees a portfolio of diverse environmental projects and supervises technical staff. -Manages client interaction and financial and resource allocation. -Provides senior project oversight and expert technical input on complex projects. -Reviews and approves project related documents and deliverables. -Evaluates subsurface characteristics for remediation projects, remedial system design, and regulatory negotiations. -Conducts Performance Reviews and project team meetings to review current and future projects, discuss project and/or employee issues, and staff workloads. Requirements: Candidates should possess a Bachelor's degree in geology, hydrogeology, environmental science, biology, or a similar scientific major. 5+ years related experience. Experience should include: investigation, reporting, remediation, and management of retail petroleum work. If the candidate does not possess experience with retail petroleum, they should have experience handling large volumes of a similar type work. Candidates should also have experience with Underground Storage Tanks (UST & LUST) and have working knowledge of New York's environmental regulations. Phase I/Phase II, report writing, client interaction, and supervision experience is a must. Candidates must be able to demonstrate the ability to manage 20-40 environmental projects concurrently. This person should be able to demonstrate that they have been able to maintain an account for an extended period of time as a result of client satisfaction. Must possess excellent communication, teamwork, analytical, organizational, technical writing, and client service skills Professional certification a plus Drug/Alcohol Screening and a Background Check are required. We offer excellent benefits and a competitive compensation program that rewards for performance and results. Our comprehensive benefits program includes: medical, dental, vision, prescription card, 401k, FSA, STD, LTD, New Parent Leave, 529 CollegeBound Fund, Tuition Assistance, Bonus Plan, Credit Union, and more.

Albany - Medication Management Systems Specialist

Aspire to achieve greatness. Greatness starts with an individual dream and is realized through action and determination to be the best. At Hospira, our vision of Advancing Wellness™ through the right people and the right products is achieved each day by more than 14,000. Our sales organization makes a significant contribution to the success of our organization by educating our customers about how our products directly address key issues they face including: providing the very best patient care, enhancing patient and healthcare worker safety, improving productivity, and targeting cost containment and reduction. We seek talented sales pros driven to be part of a team of dedicated, customer-focused individuals who aspire to excel in all that they do. Medication Management Systems Specialist In this role you will supply hospitals with IV medication management infusion device systems. Key clients will include materials management, purchasing, information technology, and nursing. You will also establish strong business relationships, influence decision-makers, monitor and assess the competitive environment, achieve territory sales goals and manage territory expenses. Your territory will be central New York. To be successful in this position, you must possess: BS/BA degree 2-5+ years capital equipment and software sales experience Travel will be required Successful sales background Project management and contract negotiations Information technology/wireless experience Clinical/Nursing is preferred with pain management/infusion pump experience Our people make Hospira an organization of stature, and we’re proud of our accomplishments. We deliver on our commitment to our communities through charitable partnerships, thoughtful giving, product donations, and global relief. We foster a culture of respect, we value integrity above all, and we empower employees to own ideas and be accountable for actions. And we reward performance with diverse avenues for growth, superior education and training, and the types of benefits you’d expect from a market leader. What do you aspire? Look closely at the work you do and consider the impact you can make at Hospira. Learn more and apply online, visit: https://sjobs.brassring.com/1033/ASP/TG/cim_jobdetail.asp?jobId=123291&type=search&JobReqLang=1&recordstart=1&JobSiteId=5100&JobSiteInfo=123291_5100&partnerid=16015&siteid=5100 Req #: 4463BR As an equal opportunity/affirmative action employer, Hospira embraces diversity of thought and cultural perspective and fosters an environment of empowerment, fairness and respect.

Albany - Geophysical Data Analyst / Interpreter

Geophysical Data Analyst/Interpreter Underground Imaging Technologies, Inc. (UIT) Underground Imaging Technologies (UIT) was formed in 2002 as a joint venture between Vermeer Manufacturing, Inc. — a leading manufacturer of surface excavation, directional drilling, construction and agricultural equipment — and El Dorado Investment Company, which is engaged in the business of providing venture capital to fund the development of innovative products and services. El Dorado is an affiliate of the Arizona Public Service (APS) Company. UIT develops and integrates hardware and software systems for mapping and investigating shallow underground utilities, features and structures. UIT was created to address two major classes of problems: (a) prevent damage during underground construction activities, and (b) enable effective management of subsurface infrastructure assets. UIT deploys its technology to provide comprehensive 3D imaging and mapping services that significantly improve the safety, accuracy and efficiency of operations related to the design, construction and management of the underground infrastructure. UIT’s integrated technology includes unique, proprietary geophysical hardware and software – including multi-channel GPR arrays; synchronized, multi-sensor TDEM (electromagnetic) devices, and centimeter-accuracy GPS and laser-positioning systems, – as well as highly developed processing, 3D imaging and feature-identification software. These components are used in acquiring, processing and interpreting underground data efficiently to produce accurate 3D images and maps. We are recruiting highly motivated individuals to serve as data analysts in the Latham, NY (Albany area) or Pella, IA (Des Moines area) offices. Candidates must be able to integrate fundamental knowledge about geologic and geophysical data to rapidly produce high quality interpretations of shallow infrastructure and geologic features. The candidate should also be knowledgeable in aspects of geophysical data collection and processing, have a familiarity with general field surveying, and be able to demonstrate a basic understanding of underground utility installation. Duties and responsibilities: The person selected to fill this position is expected to perform one or more of the following activities, depending on the assignment, and to possess specific skills that contribute to UIT’s success: 1.Conducts in-depth analyses of geophysical data to produce results that can be integrated into CAD presentations to form three dimensional maps of subsurface infrastructure. The ability to evaluate large amounts of data rapidly and to develop results tailored to clients’ requirements is essential. 2.Assists in the collection of high quality geophysical data using UIT’s proprietary hardware and acquisition software, along with other commercially available instruments. 3.Ensures that industry best practice and appropriate advanced technology is applied. 4.Prepares reports and oral presentations of study results for review by management. 5.Assists in training less experienced analysts through discussions, work sessions and example. 6.Attends meetings and conferences that contribute significantly to advancing the individual's expertise and value to UIT. Minimum Requirements: A.Bachelor’s degree required in Geophysics or related field (e.g., Geology, Physics, Mathematics, Electrical Engineering or other science or engineering field). Graduate study or additional formal training in specialty field is desirable. B.May have up to 5 years of professional experience, although candidates having recently completing their undergraduate degree are encouraged to respond. C.Possess strong oral and written communication skills and be able to contribute in a team environment. Must be proficient and comfortable in preparation of oral and written reports to clients. Document and present results of technical work to teammates, management, partners and clients, as needed. D.Ability to apply state-of-the-art interpretation and evaluation technologies toward the delivery of integrated subsurface models. E.Must demonstrate self-motivation as well as a strong work ethic: has the initiative to work without direct supervision, showing innovation in selecting and utilizing the proper tools in a fast-paced work environment, in both the field and office. F.Liaise with industry partners and clients on key technical issues as required. G.Ability to collect high quality geophysical data in challenging environments. H.Creative and imaginative. Willingness to investigate new concepts and technologies, and share ideas with team members. I.Results oriented with a commitment to meet the demands of a challenging analysis program.

Albany - Research Analyst

Classification: Full Time Compensation: $90,000 to $150,000 per year Rare opportunity in the Albany area! A prominent financial services company is seeking an Equity Analyst. Responsibilities include: conducting market research and making buy recommendations to the Director of Research and President, various market research projects, helping to manage an extremely large portfolio, maintaining business valuation models, and other duties as assigned. Relocation assistance may be offered for the right candidate. Job Requirements

Albany - 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.

Albany - Research Analyst

Classification: Full Time Compensation: $90,000 to $150,000 per year Rare opportunity in the Albany area! A prominent financial services company is seeking an Equity Analyst. Responsibilities include: conducting market research and making buy recommendations to the Director of Research and President, various market research projects, helping to manage an extremely large portfolio, maintaining business valuation models, and other duties as assigned. Relocation assistance may be offered for the right candidate. Job Requirements

Albany - Experienced in Histology or Immunohistochemistry?

Are you a happy Histotech or experienced Laboratory Researcher? Are you Interested in other opportunities your career path may lead? The field of Histotechnology is in a major growth stage and your talents are in high demand. Most of us are aware of the typical lab job but there are other opportunities out there. We need people skilled in histology and Immunohistochemistry to provide technical support, troubleshooting, and installation services to the clinical lab. How to recognize if this type of opportunity is right for you: *Do you enjoy people interaction and training others? *Would you like some variety to your daily routine, getting the opportunity to travel to different labs. *Do you thrive on the challenge of solving technical problems and helping others? *Are you looking for the opportunity to network with others in your field? *Are you interested in opportunities that have multiple career path options? If you answered yes to any of these questions our positions might be right for you! We have numerous Histo/IHC technical support opportunities come up across the nation, currently we have opportunities in your area! These positions do require 3 to 4 nights per week travel. Company provides 6 weeks training program, great on the job support, competitive salary, company car, cell phone, laptop, and complete medical package. All applicants must have at least 1 year experience in Histology or Immunohistochemistry to be considered. If you are interested in any of the above opportunities or would like to be considered for opportunities that become available in your area, please submit your resume (word format) in response to this posting.

Albany - Project Geologist

A B.S. Degree in Geology or a related environmental discipline and 4+ years of related experience or a M.S. Degree and 3+ years related experience Must possess excellent communication, technical writing, and analytical skills Professional Geologist (PG) Certification is preferred. To apply for this position go to http://www.zenjobz.com

Albany - 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.

Albany - Senior Research Specialist

RPI is seeking a Sr. Research Specialist to perform research in material science with a focus on computational and experimental studies of structural, mechanical, thermal and gas barrier properties of polymers and nanocomposites. Candidates must have a PhD in Physics, Polymer Science, or related area, with substantial research accomplishments in aforementioned research area, and demonstrated exceptional potential for outstanding research, including at least 5 years experience in simulation and modeling of nanostructures. Annual Salary is $42,723. To apply, send resume, cover letter and 3 references by November 10th, to Danielle Belser, MRC, RPI, 110 8th Street, Troy, NY 12180. We welcome candidates who will bring diverse intellectual, geographical, gender and ethnic perspectives to Rensselaer’s work and campus communities. Rensselaer Polytechnic Institute is an Affirmative Action/Equal Opportunity Employer.

Albuquerque - Regulatory Affairs Director

POSITION SUMMARY: Responsibilities include but are not limited to regulatory oversight of the company’s compliance with the FDA and international regulations on the Quality System, Safety, Medical Devices, investigational devices, GXP, Labeling, Advertising, Promotion, on-market vigilance, FDA submissions, FDA inspections and enforcements. Review and interpret regulations and ensure they are communicated through company’s policies and procedures. Other responsibilities include leading on-market vigilance investigations, participation in Complaint processing and communications to FDA and customers, preparing and submitting all MDR’s and associated documents to the FDA and other regulatory bodies. Interact with the FDA and regulatory bodies on all MDR matters. It also includes participation in manufacturing activities as well as support to design, validation, and clinical/non-clinical studies and the development of regulatory plans and reports. ESSENTIAL JOB FUNCTIONS: Handle routine regulatory activities including but not limited to the following: •Review and interpret regulations and ensure they are communicated through company’s policies and procedures. •Provide regulatory oversight of the company’s compliance with the FDA and international regulations on the Quality System, Safety, Medical Devices, investigational devices, GXP, Labeling, Advertising, Promotion, FDA submissions, 0n-market vigilance, FDA inspections and enforcements •Develop regulatory strategies, plans, templates and reports and present to management •Manage the FDA and Customer communications process for products put on quality hold. •Track submissions, initiating internal communications to adequately respond to agency inquiries and requests. •For on-market vigilance lead the complaint investigations and assign departmental responsibilities. •Manage the MDR reporting system, to ensure compliance with all aspects of the MDR regulations and ISO, requirements. Interact with the FDA and regulatory bodies on all MDR matters. •Develop and manage the annual regulatory reporting requirements to ensure compliance with all aspects of PMA and Medical Surveillance regulations. •Provide overall regulatory support to management. •Provide regulatory support to final product release. •Provide regulatory support to new product development, clinical trials, and manufacturing. •Provide Marketing and Sales with regulatory support on labeling, advertising and promotion. •Participate in the company’s management review meetings in order to determine effectiveness of the Quality System. •Work as a team member to ensure that department and company goals and objectives are met. Comply with department and company training requirements. AUTHORITIES: Approval authority for regulatory related documentation including, but not limited to FDA filings, EC filings, 0n-market vigilance, MDR, FDA and customer communications, SOPs and labeling, advertising and promotional materials. ACCOUNTABILITIES: This position is accountable for the overall regulatory compliance of the facility. JOB REQUIREMENTS: Minimum 5-year experience in US Regulatory field. Post-market medical vigilance experience is a must. International regulatory experience is a plus. Need to have proven effective communication and reporting skills with internal and regulatory organizations. EDUCATION: Minimum Bachelor’s degree in a biology or chemistry related discipline. R.A.P.S. certification as Regulatory Specialist. Level III, is a plus. EXPERIENCE: Requires experience as a regulatory generalist in all aspects of Regulatory Affairs in an FDA regulated environment (preferably medical device manufacturing) with a minimum of five years experience in a general regulatory position. Knowledgeable of regulatory agency audits (FDA and/or ISO) and the responses required. Skill in communicating recommendations to management and enforcing regulatory policies required. Candidate must have a thorough working knowledge of Quality principles and regulations as they relate to cGMP manufacturing, Quality System, 0n-market vigilance, MDR’s, Labeling, advertising, promotion and customer communications. SKILLS: •Ability to communicate clearly and effectively with internal and external contacts, superiors and peers. •Strong organizational, communication, and leadership skills. •Excellent analytical skills, judgment, and a strong understanding of regulatory techniques. •Proficient in Microsoft Word and Excel (Microsoft PowerPoint, Project and Visio desirable).

Albuquerque - Wildlife Relocation Field Manager

This is a posting for a potential position that may be created by a private firm with the intention of relocating prairie dogs from a high profile government location. The initiation of this position is dependent on the submittal of a winning bid, which is not guaranteed. The company owner has been performing prairie dog relocations for 4 years and has worked extensively in the field across northern New Mexico. This is a full-time active managerial position (40 hours/week), meaning that the manager will work alongside 1 or more employees as well as being responsible for planning, work schedules, etc. This position is for a term no less than 6 months and no more than 8 months, beginning March 2008. Responsibilities: - Plan and supervise prairie dog capture using two methods (training provided) - Submit reports to Project Manager - Manage relocation of prairie dogs into relocation area (training provided) Requirements: - Pass a 10-year FBI background check (required and only viewed by government agency, not this company) - Get appropriate vaccines necessary for working in an FAA regulated area - Attend all training - Have experience in management, demonstrated ability to lead - Ability to work during the summertime outdoors for prolonged periods - Valid driver's license - Comfortable working/handling animals and performing tasks such as cleaning cages - Your own personal vehicle for transpiration to/from work Bonus Considerations: 1. A truck or SUV that you would be willing to use for transporting animals 2. A reliable crew member who can work for you Compensation: $15+/hour, depending on responsibility, eligible for raises by demonstrating ability to stay on schedule. Covered under worker's compensation, general and auto liability; no health benefits. If you are interested in this position, please respond to this posting with your name, contact information, and either a resume or a description of how you are qualified for this position. Eco Solutions, LLC

Albuquerque - Systems Engineer

InLight Solutions, Inc. is a dynamic biomedical device company whose mission is to revolutionize the field of medicine with the introduction of noninvasive, optical technologies for blood measurements. We have an immediate opening for a Systems Engineer. The systems engineer will report directly to the Glucose Program Manager and work closely with scientists and optical engineers to: ·Design, develop and integrate high performance electronic, optical and embedded software subsystems ·Coordinate and oversee technical efforts to ensure that subsystems are designed to meet performance, cost and schedule ·Define and validate subsystem design requirements ·Direct, identify and perform system design tradeoffs ·Validate subsystem and integrated system performance ·Monitor and report on status of design/implementation progress ·Troubleshoot system issues, propose and implement solutions The qualified candidate will have: ·PhD or MS in an engineering discipline with 3 to 5 years directly related experience ·Demonstrated experience with spectroscopic measurement systems ·Demonstrated team leadership and project management skills ·Experience with embedded systems, C, Linux, Matlab and Visual Basic The preferred candidate will also have: ·Outstanding interpersonal communication skills ·Demonstrated ability to work effectively in a multidisciplinary environment ·Ability to gather and integrate technical information and inputs from multiple sources including in-house experts, scientific literature and vendors

Albuquerque - Geologist for Exploration Drilling

Immediate opening for exploration geologist to supervise long-term drilling program and conduct core logging onsite. Responsibilities include: •Participate with geology team in planning exploration protocols •Oversee and direct drill site crew according to established protocols •Complete core logs using proprietary software via iPAQ Pocket PC •Prepare and update geologic maps for potential future drill sites •Work as part of a team under general supervision •Communicate effectively, orally and in writing, across geology, drilling and management teams •Prepare management reports as needed REQUIREMENTS: •Education: 4-yr degree in geology, Masters preferred •Experience: 2 – 5 years as exploration geologist •Competency: GIS, spreadsheets, word processing, ACCESS database •Physical: Work outdoors in 12-hr shifts in various weather conditions; prefer 20 days on/10 days off; regularly lift more than 35 lbs. •Relocation preferred COMPANY OVERVIEW: Liberty Star Uranium and Metals Corp. is a publicly held exploration stage company focused on uranium and other valuable metals and minerals in northwest Arizona and Alaska. Previous production near the company’s North Pipes Super Project in northwestern Arizona yielded some of the highest grade uranium deposits in the world. Exploratory drilling should commence on the company’s North Pipes claims in December 2007, and is expected to continue for several years. Liberty Star has positioned itself well to take advantage of the rising price of uranium. The world price of uranium has increased nearly 1,000% in the last five years, primarily because of the dwindling world supply and increasing demand. Senior management has over 100 years of combined relevant experience to capitalize on this opportunity. http://www.libertystaruranium.com

Albuquerque - 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.

Albuquerque - Director of Molecular Diagnostics

POSITION SUMMARY: The Director of Molecular Diagnostics is responsible for the development and validation of molecular diagnostic assays, including tests to quantitate mRNA and tests to detect genetic variation via DNA hybridization. The Director will closely collaborate with the cytogenetics laboratory which is developing a variety of fluorescent in situ hybridization assays. ESSENTIAL JOB FUNCTIONS: •Lead a group of scientists conducting studies in the broad field of molecular diagnostics •Work closely with computational sciences in translating markers into commercially viable diagnostic assays •Develop a variety of molecular diagnostics assays •Thoroughly validate the performance characteristics of developed assays •Support clinical studies verifying and validating the developed assays •Work with product development and the Design Control Team to transfer assays to manufacturing •Contribute scientific and technical leadership to the strategy for obtaining FDA clearance for assays •Assure compliance with the quality control/quality assurance program during all stages of development •Interact with outside laboratories and medical organizations to facilitate the development and validation of molecular diagnostic assays •Assist in the education of sales and marketing personnel who represent developed assays to external clients •Work as a team member to ensure that department and company goals and objectives are met •Comply with department and company training requirements AUTHORITIES: •Review laboratory documents associated with product development and regulatory compliance •Initial and date laboratory associated documents, e.g. clinical and non-clinical validation/verification trials, equipment calibration and validation •Create and approve laboratory and departmental SOPs, plans and policies •Manage reagent, supplies, and capital purchase equipment requests •Conduct hiring and performance appraisals •Recommend promotions, positions transfers, salary requests for departmental personnel ACCOUNTABILITIES: •Laboratory associated documents, e.g. clinical and non-clinical validation/verification trials, equipment calibration and validation •Comply with company, regulatory, and quality policies •Manage laboratory operations within budget JOB REQUIREMENTS: EDUCATION: PhD or MD degree in relevant field, with an emphasis on molecular genetics, oncology and/or infectious disease and at least 10 years research experience in relevant areas. EXPERIENCE: •Minimum of five years experience laboratory management including personnel, purchasing, and creation and execution of laboratory and corporate policies •Minimum of ten years in FDA regulated environment •Successful history of interactions with computational science, clinical affairs, business development, intellectual property protection, and marketing departments •Solid background in molecular biology and genomics •Molecular techniques for genomic data collection and data mining approaches •Operational understanding of GLP and QSR SKILLS: •Ability to communicate clearly and effectively with management, peers and staff •Strong organizational, leadership, and management skills •Excellent judgment and analytical skills required for data interpretation •Technical writing skills required for creation of study reports, summaries, and manuscripts for submission to peer review journals •Strong understanding of molecular biology: oMolecular Biology: genomic and cDNA library construction and screening, sub-cloning, restriction mapping, DNA sequencing, Southern, Northern, and Western blotting, Polymerase chain reaction, Radioisotope and fluorescent probe labeling •Gene expression microarray hybridization and data collection •Data Mining and Computational Analysis SUPERVISORY RESPONSIBILITIES: •Supervise Molecular Biology Scientists and other department staff as company grows EQUIPMENT TO BE USED: •Personal computer including typical word processing and spreadsheet software •Online database searching including genomics data and scientific publications •Laboratory equipment: oAnalytical balance, opH meter, oautomatic pipettors othermocyclers ocentrifuges owater baths oshaking incubators oincubating ovens ogel electrophoresis and power supplies ophotographic gel documentation owater purification apparatus oautoclave olaboratory refrigerators and freezers (-20°C and -80°C) ophotocopiers ocomputers and software TYPICAL PHYSICAL DEMANDS: Requires sitting, standing, bending and reaching. Must be able to lift up to 25 lbs. Requires manual dexterity sufficient to operating standard office machines such as computers, fax, calculator, telephone and other office equipment. Requires normal range of hearing and vision. Must be able to stand and sit for prolonged periods of time. Must be willing to work with potentially hazardous chemicals TYPICAL MENTAL DEMANDS: •Must be able to process and interpret experimental data to arrive at sound conclusion •Must be able to interpret statistical information •Must be able to perform simple and complex math equations •Must be able to work in a noisy environment •Must be able to accomplish multiple tasks on tight deadlines WORKING CONDITIONS: Works in both a laboratory and office environment. Must be available to work evenings and weekends under tight deadlines

Albuquerque - Resource Efficiency Manager

engineering-environmental Management Inc.(e2M) has the following career opportunity available: POSITION NO: NM012 POSITION DESCRIPTION: RESOURCE EFFICIENCY MANAGER POSITION LOCATION: IMMEDIATE OPENING IN CLOVIS, NM Immediate opening in Clovis, New Mexico, for a Resource Efficiency Manager to manage the energy program for a federal client. The Resource Efficiency Manager will be responsible for compiling data, investigating energy usage and concerns, and discussing and reporting the use of energy and its’ efficiency throughout the facility. This position’s responsibilities include coordinating and building a rapport with on-site teams to educate, monitor, create economic energy goals and policies, publicize, and fully implement energy saving techniques. Successful candidates will have at minimum, a Bachelor’s Degree in a science, engineering or related field, as well as have experience in energy management, to include heating, ventilating and air conditioning (HVAC) systems. Strong experience in technical writing, data analysis, researching, communicating, and presentation abilities are required. Computer experience with the Microsoft Office Package, as well as the ability to generate presentation materials within it, are required. Experience in training and marketing are also desired. Past military or facility operations experience is a plus. If you are interested in joining the e2M team, please submit your resume and salary requirements to careersuccess@e2m.net. Please reference Position Number NM012 in the “subject” line of your email or letter. EOE

Albuquerque - 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

Albuquerque - Senior Staff Scientist, Pattern Recognition and Image Analysis

Responsibilities: Develop, implement, and optimize new image processing and pattern recognition algorithms for verification, identification, and spoof-detection based on multispectral fingerprint images. Key player in the planning of tests performed on sizeable volunteer populations. Responsible for the analysis and interpretation of data generated in such studies. Use the findings from such studies and other experimental work to improve and/or verify algorithmic performance. Works with: * Software engineering to implement computationally efficient algorithms * Marketing to develop solutions meeting customer needs & product constraints * Human testing to setup studies to evaluate and optimize performance characteristics Professional experience Minimum 8 years of relevant, post-degree industry and/or academic experience. Demonstrated capability of implementing a variety of image processing and pattern recognition algorithms. Familiar with data-driven modeling and statistical classification methods (e.g. discriminant analysis, Bayesian methods, support vector machines, neural networks, etc). Knowledge of linear and nonlinear image processing techniques. Ability to program in Matlab, C++, and/or other modern languages required. Familiarity with multispectral imaging desired. Familiarity with biometrics, particularly fingerprints, desired. Professional qualities * Creative and innovative * Goal-oriented problem solver * Data-driven and detail oriented * Able to efficiently understand, test and optimize complex algorithms as part of a larger system Education PhD with 7-10 years of industry experience.

Albuquerque - 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.

Albuquerque - Natural Resources Planner

Natural Resources Planner Albuquerque, New Mexico Description: SWCA Environmental Consultants is a growing employee-owned consulting firm specializing in environmental regulatory compliance, natural resource management, cultural resource management and related research. We are a Top 500 Design Firm and Top 200 Environmental Firm according to the latest Engineering News-Record rankings. SWCA is a company of biologists, geologists, archaeologists, paleontologists and planners with more than 25 years of experience and 350 employees located in 20 offices throughout the U.S. and the Pacific Islands. We offer an informal, team-oriented work environment, competitive salaries, and a competitive benefits package, including a stock ownership plan. SWCA is actively seeking to fill the position of Natural Resources Planner to work in the Natural Resources Program of the Albuquerque office. The position is a regular, full-time hourly position working on a variety of projects including riparian habitat restoration planning, wildfire planning, watershed planning, and NEPA compliance; the position may also require the ability to complete data collection, coordination of field efforts, report writing, and other biological and environmental planning tasks as needed. Salary and benefits will be based on individual qualifications. Responsibilities: Responsibilities for the Natural Resources Planner position include: •Assist in the writing and development of complex natural resources planning and management documents, including riparian habitat restoration, wildfire, and watershed monitoring; •Lead and complete tasks required for the completion of environmental compliance documents, including NEPA Environmental Impact Statements (EIS) and Environmental Assessments (EA), Endangered Species Act (ESA) Biological Assessments (BA), and Clean Water Act Section 404 and 401 permit applications; •Record data on field site forms or other forms and prepare reports for Natural Resource studies; •Assist project managers in data organization, interpretation, and report preparation; •Locate and use existing reports, scientific studies, data, and other relevant documents for preparation of scientific background reviews; •Work closely with SWCA Program Directors and project managers to promote SWCA’s business interests in adherence to its mission, vision, and values. Qualifications: Minimum of a Bachelor’s degree in biology, ecology, natural resource management, or related field, with two years experience in natural resource planning, including NEPA, watershed management, habitat restoration or wildfire planning. Candidates must have experience in writing environmental reports. Flexibility and willingness to learn company procedures, and ability to try new, innovative techniques, and to make independent decisions when appropriate to the situation or make adjustments as a member of a team in order to complete tasks in the most efficient and accurate manner. How to Apply: Applicants will be accepted until the position has been filled. Please send a cover letter defining your objectives, your resume and at least three (3) professional references to: Jason Gerster Recruiter SWCA Environmental Consultants 3033 N. Central Ave., Suite 145 Phoenix, AZ 85012 602-274-3958 Fax recruiting@swca.com Visit SWCA’s web site, www.swca.com, and discover why SWCA is a great place to work for environmental professionals interested in sound science and creative solutions. SWCA is proud to be an Equal Opportunity Employer and encourages women and minorities to apply.

Albuquerque - 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

Albuquerque - Research Scientist

Research Scientist Position based in White Sands, NM JOB DESCRIPTIONAdvanced formal training in remote sensing and/or earth science, engineering, math or a physical science. Familiarity with the overall mission community and experience in applicable sensor discipline.Demonstrated experience and knowledge in the use if applicable COTS processing software and technologies.practical experience with ERDAS, ENVI, Remote View, Matrix, CASE Exec, IMX, REX, or equivalent Applicants selected will be subject to a government security investigation and must meet eligibility requirements for access to classified information. QUALIFICATIONSFamiliarity with the overall mission community and experience in applicable sensor discipline.BENEFITSA Total Value package.There is much to be said about the Lockheed Martin Total Value package. Part of the package involves a commitment to develop top talent from within as well as provide access to a wide range of training programs and services. There is also the opportunity to work in exceptional environments marked by: Project Significance * Quality People * Recognition * Learning and Development * Internal Career Mobility * Competitive Pay * and Excellent Benefits.A commitment to your work/life balance.Part of the Lockheed Martin experience includes a focus on work/life satisfaction. We offer programs and policies that include: Flexible/Alternative Work Schedules and Casual Dress at many locations * Telecommuting * Tuition Assistance * Employee Assistance Program * Fitness Centers * Birth/Adoption Leave * Domestic Partner Benefits * and Adoption Assistance.COMPANY PROFILEAt Lockheed Martin, we are driven by innovation and integrity. We believe that by applying the highest business ethics and visionary thinking - everything is within our reach, and yours.We invite you to explore the possibilities with one of the foremost systems engineering, software and systems integration companies in the world.Exceptional choices in careers, challenges, and locations across the nation.Lockheed Martin Aeronautics CompanyJoin in designing, building and supporting the world's most sophisticated military aircraft. Your involvement may include: The multiservice F-35 Joint Strike Fighter (JSF) * The proven multirole fighter, the F-16 *Lockheed Martin Space SystemsLay the foundation for future space systems. A sampling of programs includes: The world's most powerful and advanced telecommunications satellites for government, civil and commercial interests *Lockheed Martin Electronic SystemsPioneer, integrate and deliver cutting-edge technologies across three key areas: maritime systems and sensors, missiles and fire control programs and platforms, training and transportation solutions *Lockheed Martin Information Systems & Global ServicesDelivers world-class solutions and advanced technology globally across a broad spectrum of domains.Diversity and inclusionWhat we believe...what we live. You will find that we are both a uniquely diverse and unified team; reflecting many cultures and points of view.An Equal Opportunity Employer.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=R6989116906055

Altoona - 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!

Altoona - Assistant Scientist

POSITION SUMMARY: Assistant Scientist works in collaboration with others on procedures, methods, data analysis and documentation of that work. Basic understanding of techniques is required. Position should accept supervision well and work effectively with other personnel to accomplish tasks and experiments. Problems are of moderate scope, with analysis of situations or data requiring a review of routine identifiable factors. Judgment is exercised within defined procedures and practices to determine appropriate actions. Position assists in the preparation of technical reports, summaries, protocols, procedures and quantitative analysis. Maintains proper training identified for position, performance is consistent with GMP and established facility requirements. The ability to record results accurately and perform analysis of data, to exercise independence and present ideas for modifying existing procedures is essential. Skills/Requirements EDUCATION AND RELATED EXPERIENCE: A B.S. or equivalent in an appropriate scientific discipline with 0-2 years of related laboratory, manufacturing or research experience. ESSENTIAL FUNCTIONS: Basic understanding of simple laboratory techniques following GMP practice is required. They should accept supervision well and work effectively independently or as a member of a team toward established timelines for completion of tasks and experiments. Consistent, timely and accurate documentation of duties performed as well as analysis of data and making routine determinations. TECHNICAL SKILLS: GMP performance and documentation. Skills specific to identified work area. 6 month assignment IF QUALIFIED, PLEASE SUBMIT RESUME AND SALARY REQUIREMENTS

Altoona - QA Associate

Job Description Responsible for the administration of product quality complaints and related investigation activities for Biotech products in compliance with 21 CFR 211.198 and in support of the Quality organization. Maintains processes for effective receipt of complaints from Medical Information, Customer Contact Center, business partners, outside contractors, and other sources as applicable. Performs reporting activities to summarize complaints for all levels of management. ESSENTIAL FUNCTIONS: • Receives, evaluates and processes complaints. • Initiates contact with complaint source to obtain all relevant data. • Enters data in database, performs trending analysis and requests batch record review. • Ensures through complainant, return of product to QA. Inspects, confirms, documents/photographs and catalogs samples returned. • Coordinates investigation process with Process Science and/or contractors, sending vial samples and other relevant documentation and information to appropriate parties. • Tracks progress of complaints/investigations and communicates with all involved parties regarding status. • Organizes meetings with vendors, contractors and management to review issues (e.g., overdue, incorrect investigation, etc.) • Prepares management communication of all complaint, manufacturing or investigation issues including overdue and update information. • Analyzes all components of completed complaints to determine root cause and corrective action. Summarizes complaint components for closure and database information. Sends letter/corrective action to complainant. • Advises Sales Administration of product replacement needs once product samples are received in QA. *This is not an exhaustive or comprehensive listing of job functions. May perform other duties as assigned. *ADDITIONAL RESPONSIBILITIES/DUTIES: • Keeps manager informed on any complaint, manufacturing and investigation issues. • Reviews departmental SOP’s • Creates reports and summaries as needed, through database extraction/queries. • Supports tracking/database system upgrades. *This is not an exhaustive or comprehensive listing of job functions. May perform other duties as assigned AUTONOMY and COMPLEXITY Works independently on routine tasks. Needs supervision/support to resolve some complex issues. Is technically competent within job function. Has departmental focus with awareness of all Quality functions and business areas. Thinks analytically and acts decisively. NATURE OF TASKS: Mid-level position. Independently performs activities. Identifies issues and implements resolutions. Assesses data. Prepares and reviews documentation independently. Authors and/or revises SOPs. Applies complex mathematical analysis and skills. Provides input to Biological Product Deviation Reports, Annual Reports, Annual Product Reviews, and safety reports. Provides training for Sales Representatives on complaint reporting processes Skills/Requirements EDUCATION AND EXPERIENCE: Bachelor’s Degree in Biology, Chemistry or other Science discipline or equivalent work experience. 3 - 5 years experience a regulated manufacturing environment, preferably in biotechnology or pharmaceutical industries. 2+ years of Quality Assurance and/or Control experience. Strong communication, organizational and project management skills. Prior demonstrated success at QA Associate I Level, or equivalent. LANGUAGE SKILLS: • Ability to read, analyze and interpret any combination of simple, business, professional, technical or governmental documentation. • Ability to write, business reports, correspondence, or procedure manuals using original, prescribed, or innovative techniques or styles. • Ability to effectively present information and respond to questions from groups of managers, clients, customers and the general public. • Ability to respond to common or complex inquires or complaints from customers, regulatory agencies or members of the business community. REASONING ABILITY: • Ability to interpret and carry out a variety of instructions from standardized situations to varying degrees of technical complexity furnished in written, oral, diagram or schedule form. • Ability to define and deal with problems, collect data, establish facts and draw valid conclusions from standardized situations COMPUTER ABILITY: • Ability to utilize software and customized programs to meet business needs. • Ability to utilize and customize software and troubleshoot to resolve minor software and hardware problems MATHEMATICAL SKILLS: • Ability to add, subtract, multiply and divide in all units of measurement, using whole numbers, common fractions and decimals, as well as compute rate, ratio and percent and to draw and/or interpret bar graphs. • Ability to calculate figures and amounts such as proportions, percentages, area, circumference and/or volume OTHER SKILLS, ABILITIES OR QUALIFICATIONS: • Advanced computer skills, including data entry and database management • Advanced skills in Microsoft Office (Word, Excel, Access) • Excellent written and oral communications skills *PHYSICAL DEMANDS: While performing the duties of this job, the employee: • Needs to be mobile and able to independently transport themselves between various sites/locations, as dictated by the essential functions and responsibilities of the position. • Is frequently required to talk and hear. • Must be able to identify and distinguish colors. 6 month assignment

Altoona - BioPharma Clinical 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

Altoona - Clinical Production Supervisor, Global BioPharma Co.

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

Amarillo - Lead Clinical Research Associate(TX)

Urgent requirement for one of the our top client located in 'TX '. Please contact me at your earliest convenience, along with job No. to glenn.davis@vernascientific.com. Job Description: Responsible for the initiation, monitoring, completion and reporting of clinical studies. May supervise the activities of other monitors as a Lead CRA. · Initiates, monitors and closes-out study sites with moderate to large size and complexity, promoting high quality performance as measured by protocol adherence, accurate study documentation, achievement of enrollment milestones and a high level of evaluable data. Contributes to and implements quality clinical monitoring plans that meet protocol objectives. · Maintains high quality and timely sponsor records. Ensures that the information in databases allows for rapid database locks; works effectively with clinical data management and other groups to resolve database issues; contributes to the data evaluability process. · Provide advanced level of monitoring; provides progress reports, handles complex field problems with study sites, internal support groups and clinical project managers. identifies trends in data and process improvement opportunities. · May contribute to the writing and design of protocols, case report forms and other study materials with supervision. · Communicates effectively with key opinion leaders, clinical investigators and their staff, IRBs, clinical contractors and other vendors in order to meet protocol objectives and enhance relationships; communicates clearly and provides accurate instruction and guidance. Requirements: Either 1.R.N. certification with 12 years of clinical research experience, including 9 years of direct CRA experience may be considered. 2.Bachelor's degree in an appropriate discipline and upto 9 years related experience, including 6 years as a CRA 3.Master's degree in an appropriate discipline with 6 years related experience, including 2 years experience as a CRA 4.Ph.D. with 3 years related experience, including 2 years experience as a CRA Contact: The most effective way of communication is via email please forward us your updated WORD FORMAT resume (Address, Contact number and email is must) Please mention your best hourly rate, availability and visa status. Any questions, do feel free to email us to glenn.davis@vernascientific.com. About Verna Scientific: Verna is a multidisciplinary Life Sciences firm, Verna specialize in Consulting and Staffing services for Fortune 1000 as well as start-up companies in Biotech, Pharmaceutical and Healthcare industries with major focus on clinical research and data management. Verna is growing rapidly and we are always looking for individuals with outstanding capabilities in clinical arena. We offer careers in both technology and research disciplines. Verna's expertise has earned us an esteemed reputation within the industry and with our clients such as Schering-Plough, Astra Zeneca, Purdue, Abbott Labs, Merck, Wyeth, Allergan and Amgen. Please visit us on the web at www.vernascientific.com Key words: Clinical research associate, clinical research assistant, clinical data manager, clinical research scientist, clinical research coordinator,clinical data analyst, clinical trail manager, clinical project manager, biostatistician, statistical analyst, sas programmer,regulatory affair specialist, regulatory affairs associate, quality analyst, associate director, medical director, senior clinical trail specialist,validation. Compliance, clinical data specialist,statistical programmer, principal,Director

Ames - Product Development Scientist

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 Telephone and face to face interviews to be scheduled immediately with company.

Ames - Bioprocess Asst

Position assists in efficient fractionation of bovine plasma into high purity scientific products for diagnostic, pharmaceutical, and research markets in compliance with FDA, USDA, and OSHA. 2-4 year degree in chemistry or other science preferred. High aptitude and interest in math, chemistry, computer usage. Ability to operate forklift, maintain valid driver license. Frequent lifting up to 60 pounds, frequent testing in lab, data recording, cleaning. Must have solid oral/written communication skills and ability to comprehend instructions. Entry level position w/room for growth. EOE.

Ames - Validation Engineer

Compliance Team, Inc. has exciting opportunities for Validation Engineers in various locations. We seek top-notch professionals who have a diverse validation experience with process equipment qualification and control system qualification in the biotech, pharmaceutical and/or medical device industry experience. Responsibilities: The responsibilities include preparing/executing installation/operational/performance qualifications for plant equipment, facilities, utilities, process control systems, computer systems, cleaning validation, and process validation activities in support of GMP / FDA requirements. Requirements/Qualifications •Bachelors degree in Engineering, Science, or Computer Science. •2-5 years experience in FDA related manufacturing or laboratory operations. •Familiarity with validation concepts, procedures, protocols and requirements. •Knowledge of FDA regulations, pharmaceutical GMPs (21 CFR 210 and 211). •Familiar with pharmaceutical manufacturing process, facilities and equipment, calibration, IQ, OQ, PQ, development of SOPs. •Experience with process control applications is desirable. •Excellent organizational and time management skills. •Excellent decision making and creative problem solving skills. •Ability to develop, organize, and manage multiple tasks. •Computer proficiency in MS Office software In addition to the above technical competencies, ideal candidates will have a commitment to quality service excellence along with outstanding interpersonal, oral, and written communication skills. Candidates must be results-oriented, able to make decisions, and able to prioritize work per business needs. Strong communication, organization, and time management skills are necessary. Desired skills include: teamwork, leadership, ability to maintain constructive relationships with personnel from various disciplines at all levels in the organization. The successful candidate should demonstrate integrity, reliability, dedication, adaptability, innovation, and self-motivation. For more company information see: http://www.complianceteaminc.com/

Annarbor - SAS consultant needed for Proc mixed, using clinical data

Short-term (with possibility of more work)biostat consultant needed. Must know timeseries, repeated measure analyisis methods and issues. Must have familiarity with SAS Proc mixed. Also familiarity with sample size estimation based on power analysis. Maybe 10-20 hours work at this time. Need is immediate, with goal of rapid peer-reviewed article production. Hourly rate negotiated based on experience. Send resume and contact info to bmbrock@umich.edu, ASAP.