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Biotech, R&D, & science in Northern NJ

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  1. Product Engineer

     Top Medical Device company requires Product Engineer     Employee type: Full time permanent   Description participate on cross-functional teams to develop new Foot & Ankle products. •Interface with clinical advisors to gather input for design and evaluate new products. Model and detail implant and instrument designs utilizing Pro/Engineer. • Develop prototypes for design verification and validation. •Develop verification and validation protocols and technical reports Utilize and Manage design ...

  2. Clinical Data Specialist - 104945

    Task Based Trial Data Contractor – 6 month contract The task based contractor is responsible for day-to-day activities.  Some specifics include: The task-based person helps clean specific data (example SAE reconciliation, Local Labs reconciliation, do manual review, and query data from listings and reports).  The task-based worker will assist TDM in cleaning data and is not the lead on the study. Responsible for providing timely and professional ongoing quality management of clinical trial data ...

  3. Regulatory Affairs Specialist

     Our client in Mahwah, NJ is seeking Regulatory Affairs Specialist. This is an immediate need. Kindly respond to this positing if you are interested. Regulatory Affairs Specialist BA/BS in Scientific discipline required. Engineering strongly preferred RAC certification desired Plan, organize and implement strategies and activities required to procure regulatory approval for new and revised product lines. Participate in cross functional team activities from initial stages to securing govenrment ...

  4. Quality Engineer- Medical Device

    Lead Quality Engineering activities for design, development, manufacturing and/or distribution of orthopedic implants and instruments to ensure a high level of process and product quality. • Ensure high level of compliance to FDA QSR/cGMPs and ISO 13485 in all assigned areas. • Work closely with internal departments (Operations, Advanced Operations, R&D, and Distribution) to resolve in-house and supplier quality problems using established problem-solving methodologies (Root Cause Analysis, Mistake ...

  5. Engineering Technician

    Candidates cannot begin an assignment without successful completion of drug and background clearances.   2 Month Contract Assignment   $14.00 Hourly   Qualifications: Proficient in reading and understanding test instructions. Understanding of GMP and ISO, documentation control. Experience with mechanical test equipment (Instron) and digital balances. Knowledge of self-injection devices.   Responsibilities: Product development and feasibility testing of pen self-injection and syringe systems ...

  6. Product Development Technician (7191)

    The Advanced Product Development Services group, which supports all product development and product engineering platforms across MSS, is looking for a talented, meticulous, and passionate individual to help the team by way of expertise and efficiency in a variety of mechanical and leakage testing of products and product packaging.  In addition to testing, this associate may also contribute to the improvement of existing testing methodologies, measurement system development & analysis, data analysis, ...

  7. Biostatistician III - 105029

    Biostatistician III – 6 month contract  Designing clinical studies. Writing and reviewing statistical sections and other relevant parts of study synopses and protocols. Support study start up activities. Develop RAP, program TLFs, preparation for database lock, dry run and CSR activities. Review CRF, DB spec, VAP. Support analyses as required for decision making at project level. Support analyses and activities during submission and response to HA questions. Coordinate study tasks with ...

  8. Clinical Trial Manager I - 105038

    Expert Clinical Manager I – 5 month contract Under the guidance of the Project Operations and Compliance (POCO) assist with organizing a structure in Novartis document and tracking systems (CREDI and clinadmin) for all our compassionate use programs. Requirements BS or MS degree required. At least 3 years’ experience in pharmaceutical industry or CRO. Be able to understand clinical operations and electronic clinical tracking systems. Be a good team player and work with multiple people from ...

  9. Associate Global Correlative Sciences Leader - 105044

    Associate Global Correlative Sciences Leader – 5 month contract Contributes to Afinitor and PI3K programs' biomarker research by supporting the programs' Correlative Science Leaders. Key expertise includes familiarity with cancer genetic (breast cancer in particular), next generation sequencing (NGS), and PI3K/AKT/mTOR pathway. Requirements PhD in cancer genetics, cancer biology and molecular biology. Pharmaceutical industry experience is desirable, but NOT required. Knowledge in ...

  10. Compound Pharmaceutical Sales Representative

      If you have experience selling compound pharmaceuticals and desire a generous & predictable income from stable pharmacies then please read on. We have clients that are looking for ethical, career minded reps that have established relationships with physicians who believe in and are currently prescribing compounded pharmaceuticals to their patients. We would prefer reps that have current relationships but will consider former compounding reps with less than a 12 month time gap out of the business. ...

  11. Genetics and Dairy Reproductives Sr. Marketing Manager

    The Sr. Marketing Manager will lead all Marketing efforts related to our client’s genetics and reproductive brands. The incumbent will lead the development of a rolling operational plan, including marketing objectives and strategies, segmentation brand positioning, pricing, brand life cycle planning, distribution, promotion and competitive action for assigned brand. Qualifications include BS or BA required. MBA or relevant advanced degree preferred. Professional experience: Five to seven years of ...

  12. DESKTOP PUBLISHER

    Our client, a large pharmaceutical company, is currently seeking a DESKTOP PUBLISHER.Responsible for publishing and managing QC for high quality scientific documentation (e.g. study reports) for submission to regulatory authorities in support of marketing applicationsPreparation of high quality scientific documentation and submission documents in accordance with the timelines specified by NIBR and in compliance to internal and external standards Completion of an adequate number of nonclinical or ...

  13. Biochemist

    We have a Contract opportunity with a prominent client for a Biochemist in Franklin Lakes, NJ.   Qualifications: A Ph.D. in cell biology, molecular biology, or related field with a minimum of 5 years of laboratory experience is required. A focus in the area of immunology and/or cell therapy is desired. Cell analysis skill sets such as flow cytometry and microscopy are required. Experience with metabolomics is preferred. General molecular biology and laboratory skills such as ELISA, immuno ...

  14. Clinical Research Scientist

     **BA/BS or advanced degree required! 3 years of experience required!** Duties:  -The Clinical Research Scientist (CRS) will support US efforts in the planning, execution and reporting of US CD&MA clinical trials in Oncology/Hematology/Rare Disease/Early Therapeutics.  -Responsible for the implementation of designated clinical trials including investigator selection, patient recruitment, preparation of trial related documentation (protocols, Case report forms, consent documents, letters of agreement ...

  15. Medical Writer needed for fast-growing pharmaceutical co - Northern NJ

    EXCELLENT OPPORTUNITY FOR EXPERIENCED MEDICAL WRITER! FLEXIBLE ON-SITE / OFF-SITE! LONG-TERM CONTRACT OPPORTUNITY! EXCELLENT WORK ENVIRONMENT!     The Medical Writer will work directly with clinical study teams, the Oncology medical writing teams, regulatory affairs personnel, and the publishing group in the preparation of scientifically valid regulatory documents. Responsibilities include prepare regulatory documents on behalf of the Company in accordance with the ICH guidelines, international ...

  16. Process Engineer

    POSITION TITLE: Process Engineer   SPECIFICATION NUMBER:  68804CRI   LOCATION: Morristown, New Jersey   COMPENSATION:    Hourly Consultant - 9 months contract  - then possibility to cross over to a permanent position paying up to $90,000 +  16% Bonus   COMPANY:    Our client is a leader in the Medical Device industry.   POSITION SUMMARY   This is an opportunity to play a key-role in an aggressive, growth-oriented Company that provides an entrepreneurial work environment in an emerging ...

  17. Researcher

    QPharma is growing.   We currently have an opening for a Researcher, to work in our corporate headquarters located in Morristown, NJ. Duties and Responsibilities: The Researcher’s duties will involve researching all 50 state laws and rules and regulations around prescriptive authority for controlled substances. The Researcher would need to be well informed of the current regulations as they exist within the 50 states, and continually track any updates/changes to the laws.  The information to be ...

  18. Registered Pharmacist ( Per Diem)

    Registered Pharmacists ( Per Diem) QPharma is expanding its pharmacy operations and services.  We are looking for  NJ licensed and Registered Pharmacists to work per diem in support of our closed door specialty/mail order facility.  Our facility  has a high volume prescription intake, and the Pharmacists will also provide trouble shooting of insurance related issues, and QA of prescriptions to get dispensed. Required Must be a Registered Pharmacist and licensed in the state of NJ Be able to ...

  19. Senior Account Executives

    QPharma, Inc., is growing!  We have openings for Senior Account Executives within our Commercial Services division.  In this role, the Senior Account Executive will report to the Client Services Manager and provide leadership to other team members. The Senior Account Executive will be a strategic, smart communicator who develops, builds and maintains strong relationships with clients. Duties and Responsibilities: Responsible for overall client satisfaction as it relates to the services provided. ...

  20. Nonwovens Scientist – NONWOVEN, Consumer Research - Ramsey, NJ

    STI-ECD-561-(A) Nonwovens Scientist – NONWOVEN, Consumer Research - Ramsey, NJ Location: Ramsey, NJ Domain: Textile Job Type: Direct                           Job Description: Nonwovens Scientist will assist the Manager in the development and implementation of unique and advantaged technologies to support the product roadmap.   Job Responsibilities: The Staff Scientist will be exposed to technical intellectual property on a frequent basis. Expected to initiate/establish Confidentiality ...

  21. Clinical Research Manager II- 94440

    Minimum Requirements: Prior experience with Implementation of clinical trials in the United States safety, data consistency, trial timelines, budget, resources, eligibility and enrollment.   Education: Bachelor Degree required   Job Description: Support US efforts in the planning, execution and reporting of USCDMA clinical trials in Oncology. Implementation of clinical trials in the United States (safety, data consistency, trial timelines, budget, resources, eligibility and enrollment), ...

  22. SENIOR DEVELOPMENT ENGINEER: ROOFING SYSTEMS

    You are a pro at materials selection and product development for membrane roofing and waterproofing systems; that’s why we need you to help keep us at the top of outgame! You will work with the R&D team as well as cross-functional groups to develop new products from inception through commercialization. Help us to identify new product, process and raw materials developmental opportunities for waterproofing, components and accessories. Use design of materials to plan and perform testing and ...

  23. Pharmacovigilance Submission Specialist -Contract

    Our institution is currently seeking a US Pharmacovigilance Submission Specialist Consultant. The Submissions Specialist, US Pharmacovigilance (PV) role is accountable for the final step in the single case handling process for Pharmaceuticals products. The Submissions Specialist determines whether or not any marketed or clinical development case should be submitted to the FDA. This process involves analyzing case information for report ability based on US labeling, causality, drug code and regulatory ...

  24. Product Manager

    Position: Product Manager Company:  Manufacturer of Scientific Products for use in laboratory environments End Users: Laboratories in College/University, Biotech, Research, Pharmaceutical and Government accounts Requirements: BS degree in Marketing or one of the Sciences (Chemistry, Biology, etc.) 2-5 years past experience in a Marketing role - prefer Product Manager Base salary: up to $75,000 based on experience Full Benefits package