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biotechnology in Raleigh

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    1. Biomanufacturing Associates Needed! RTP, NC

      Needed: Biomanufacturing Associates - RTP, NC Kelly Services is currently recruiting Manufacturing Associates to work within a well-established biotechnology company in the RTP area. We have several long term contract opportunities available. Successful candidates will possess a strong work ethic, ability to work independently, and a desire to grow in their career. All positions require the ...

    2. Director, Nonclinical Development

        Duties and Responsibilities: Primary responsibilities include but are not limited to the following: Operational and scientific responsibility for all nonclinical development activities, including in vivo non-GLP safety and tolerability, pharmacokinetic, pharmacodynamics, and GLP toxicological studies (encompassing both the in vivo and bioanalytical components), and support of clinical ...

    3. Technical Writer

      Sigma Bullhorn ID: 7584 Location: Sanford Area, NC Position/Role: Technical Writer Client Industry: Biotechnology/Pharmaceuticals Classification: 6 Months Contract (Extensions Likely Into 2016 or Conversion to FTP Status)   PLEASE NOTE: Remote Work is NOT allowed. On-Site Only. If you have any questions, I’ll be happy to answer them, but I’ll need to see a copy of your most ‘up-to-date’ ...

    4. Research Program Analyst

      FOR IMMEDIATE HIRE: Bennett Aerospace, Inc. (www.BennettAerospace.com) is seeking a highly motivated Research Program Analyst to provide the scientific and technical support to the Technical/budgetary Support Staff for University Affiliated Research Centers (UARCs) program at the US Army Research Office (ARO) in Durham, North Carolina (the Research Triangle). The Army’s UARC Program consists ...

    5. Laboratory Remediation - Computer System Validation Consultant

      ProPharma Group is an industry leader providing validation, compliance and technical services to the pharmaceutical, biotechnology, medical device and related industries.  We offer the excitement of a consistently evolving career.  Our team is continually learning and working on new and exciting projects in a variety of regions.  We look for people who excel in their technical area of ...

    6. Scientist III, Analytical Development

      Hello,   My name is Sarah and I represent The Fountain Group.  We are a national staffing firm and are currently seeking Scientist III, Analytical Development for a prominent pharmaceutical client of ours.  This position is located in RTP, NC. Details for the position are as follows:   Job Description: Seeking an Associate Scientist III with a strong technical background in analytical ...

    7. Project Cost Manager

      Project cost professionals with a passion for excellence. We are seeking skillful, experienced Project Cost Managers. Ideal candidates must have excellent working experience in the biotechnology/pharmaceutical industry. If you are interested in being considered for this position within the Taurus consulting team, we encourage you to apply. As a Project Cost Manager, you are responsible for ...

    8. Project Cost Controls Engineer

      Project cost professionals focused on success. We are seeking skillful, experienced Project Cost Engineers. Ideal candidates must have excellent working experience in the biotechnology/pharmaceutical industry. If you are interested in being considered for this position within the Taurus consulting team, we encourage you to apply. As a Project Cost Engineer, you are responsible for ensuring ...

    9. QC Scientist  - 12 months - (97616 KD)

        WORK EXPERIENCE/SKILLS:   MINIMUM: 4-7 yrs of intermediate Good Manufacturing Practices (GMP) experience 4 years of manufacturing, quality or engineering experience in the biotech or pharmaceutical industry.   EDUCATIONAL BACKGROUND: MINIMUM: BS/BA Degree in Science/related field or other appropriate education/experience in biotech or pharmaceutical industry. No Travel/No ...

    10. QC Associate Scientist  - 12 months - (97615 KD)

        Responsibilities may include: • Providing Quality Review/Oversight of site GMP documentation related to the operation of a vaccine manufacturing facility to ensure compliance with global regulatory agencies and COMPANY quality standards. • Performs testing including, but not limited to clinical and/or commercial product, raw materials and validation samples. • Analyzes and interprets ...

    11. Senior Clinical SAS Programmer

      OVERVIEW   Principal statistical programmer will work closely with clients and provide high level consulting services and oversight for specific projects that may include project management, assessing new technologies, process improvements, system validation, SOP development, complex statistical programming, clinical software implementations and integrations.  Principal statistical ...