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laboratory in Raleigh

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  1. Quality Control Analyst I- 3921347

    Support organization and start-up of the QC laboratory.   Execute method validation and transfers for assigned assays. Execute assigned testing. Ensure that the samples are tested according to quality requirements defined via registered specifications in accordance with local/international regulations.   Ensure results reported are valid, accurate and documented per applicable regulatory and corporate requirements.   Duties: Laboratory Function Perform assigned testing Participate in ...

  2. Validation Engineer

      Here at ProPharma Group, we work with clients in the pharmaceutical, biotechnology and medical device industries to provide the best solutions for their unique challenges and concerns. We build successful long-term relationships with clients by providing leading industry knowledge, experience, and proven processes. Our goal is to provide the information our clients need to deliver safe, effective and quality products and services every time. Responsibilities: A Validation Engineer at ProPharma ...

  3. Scientist (virology)

      Scientist  Morrisville NC 27560 6 month contract Pay rate: $26-$30/HR   Specific Duties, Activities, and Responsibilities Develop and execute laboratory work plans/schedules independently, using customer milestones and Division/site performance standards and metrics Authors technical documents, such as protocols, test methods, text reports, certificates of analysis, and operating procedures Review technical documents for accuracy, thoroughness and regulatory compliance Trains, coaches ...

  4. Associate Scientist (protein chemistry)

    Associate Scientist Morrisville NC 27560 6 month contract Pay rate: $21 - $24 per hour (based on experience) Specific Duties, Activities, and Responsibilities • Perform activities of moderate complexity involving others. Assist in the implementation of new technologies or approaches. • Occasional contact with customer technical personnel to effectively coordinate laboratory studies. • Writes summary reports with supervisory guidance. Can effectively coach or instruct technicians or lab ...

  5. QC Analyst I

     My name is Erica and I represent The Fountain Group.  We are a national staffing firm and are currently seeking someone for a QC Analyst position with a prominent Fortune 500 client of ours.  The position is located in Holly Springs, NC.  If the position sounds like it may be of interest to you, please respond with an updated resume and acceptable salary range.  I will get in touch with you to further discuss the position.   Job Description: Support organization and start-up of the QC ...

  6. 3919367 – QC Data Reviewer

    This position provides operational Phase Support organization of the QC Analytical, Biochemistry, and Raw Materials laboratory.  The successful candidate will plan and assist with required resources for day to day data review of raw data generated in the QC laboratories. You must have strong scientific and data review background as to provide technical knowledge and quality comments associated with raw data review and documentation.       RESPONSIBILITIES:   Perform timely data review with a ...

  7. Associate Scientist

      My name is Starr and I represent The Fountain Group.  We are a national staffing firm and are currently seeking an Associate Scientist for a prominent client of ours.  This position is located in Research Triangle Park, NC. Details for the positions are as follows:   Job Description:   Perform and document a variety of functions in support of the development of new technologies for cell culture manufacturing processes of human therapeutic biomolecules. Conduct laboratory cell culture ...

  8. Clinical Document Specialist

      ~~SUMMARY: • The CDS will support the Company’s regulatory function and study team in the document management of clinical research trials from the project development stage through to project completion.  Mainly, the CDS will perform a variety of research, database, and administrative duties of a routine and technical nature in support of clinical trials to assist investigators in organizing, gathering, and compiling clinical research data. DUTIES AND RESPONSIBILITIES: • Assist with collecting, ...

  9. Regulatory Affairs Specialist

    ~~SUMMARY: • The Regulatory Affairs Specialist supports the Company’s regulatory function and project teams through the provision of a variety of administrative and technical tasks involving the management of clinical research trials documentation. In addition, the Regulatory Affairs Specialist performs a variety of research, database, and administrative duties of a routine and technical nature in support of corporate initiatives and clinical trials to assist MedSource and/or clients in organizing, ...

  10. Brand Leader---OTC based in Greensboro, NC

      Reporting directly to the Head of Commercial Operations, the Brand Manager will be responsible for all aspects of the development and execution of strategic and operational brand marketing plans for products in the consumer and physician markets including Blue Lizard Sunscreen.  The candidate will manage and be accountable for the overall performance of their brands including demand management and product Profit and Loss.   Knowledge, Skills and Experience required: BS/BA degree in business ...

  11. Brand Leader- Prescription Dermatology based in Greensboro, NC

      Reporting directly to the Head of Commercial Operations, the Rx Brand Leader will be responsible for all aspects of the development and execution of strategic and operational brand marketing plans for products in our branded dermatologic prescription division.  The successful candidate will manage and be accountable for the overall performance of their brands including demand management and product Profit and Loss. Knowledge Skills and Experience Required: BS/BA degree in business/marketing; ...

  12. Head Of Analytics based in Greensboro, NC

      Crown Laboratories,  Inc. is seeking a qualified business analyst who possesses high business acumen, understands pharmaceutical sales & marketing business processes and commercial data and has the ability to adapt to rapid growth and prosper in an entrepreneurial environment. Reporting directly to the Head of Commercial Operations, the Head of Analytics will be responsible for the development, preparation, quality assurance, distribution and maintenance of standard ad-hoc reports, including but ...

  13. 3910335 - GMP/GLP Analyst

      Job Purpose: Provide assistance to support the current effort of establishing a GMP testing laboratory within Analytical Development, which includes the initial setup, GMP certification and operational readiness.       Responsibilities:   Provides general administrative assistance to support change control records opened for the GMP lab Organize and maintain a list of current quality procedures for analytical laboratory operation, testing, method development, qualification and validation, ...

  14. Quality Control Associate

      My name is Starr and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Quality Control Associate for a prominent client of ours.  This position is located in RTP, NC. Details for the positions are as follows:   Job Description:   The primary responsibility for a Quality Control Associate I is the execution of QC environmental monitoring, routine testing and all activities associated with executing this testing in a cGMP manner. Additional ...

  15. Bioengineer

     The Bioengineer will be responsible for the calibration, installation and maintenance of instrumentation in support of Sequenom Laboratories products and is the key interface between instrument vendors and the clinical laboratory. Specializing in Systems, Software, Clinical Regulatory or Technical Documentation, this position is responsible for all aspects of product serviceability and technical product documentation throughout product lifecycle.   Responsibilities: Prioritize, evaluate, and ...

  16. 3897743 - Validation Analyst II/III - Biochemistry

    Job Purpose   This position will support the organization of the QC Biochemistry laboratory at the Flu Cell Culture facility in Holly Springs, NC.   Primary responsibilities for this position include method development and validation for biochemistry assays (protein content determination by BCA, SDS-PAGE, ELISA, and UV/Vis spectrometry).     Essential Functions:   Perform and assist in the method development and validation Author SOPs, protocols and technical reports Perform laboratory ...

  17. Quality Assurance Manager GCP/GMP Operations

    Brio Resource Group is seeking a Quality Assurance Manager GCP/GMP Operations for an emerging pharmaceutical company located in the Raleigh/Durham, NC area. The QA Manager will be responsible for Clinical Trial Development projects and additional Quality Assurance Manufacturing activities.  Job Requirements: -Responsible for Clinical Supplies batch record review providing final release for use in clinical trials -Quality Assurance contact for deviations and failures -Clinical vendor selection ...

  18. Investigations Specialist

    Description PSC Biotech Corporation is a global, employee owned, life sciences consultancy that performs projects and staff augmentation in the following disciplines: Engineering, Information Technology, Technical Services, Validation, Compliance, Regulatory Submissions, Clinical, Project Management and Quality Assurance. PSC Biotech, incorporated in 1996, has been performing projects globally for over 15 years. PSC Biotech is currently looking for an Investigations Specialist for our client in ...

  19. 3888627 – QC Data Reviewer

    This position provides operational Phase Support organization of the QC Analytical, Biochemistry, and Raw Materials laboratory.  The successful candidate will plan and assist with required resources for day to day data review of raw data generated in the QC laboratories. You must have strong scientific and data review background as to provide technical knowledge and quality comments associated with raw data review and documentation.       RESPONSIBILITIES:   Perform timely data review with a ...

  20. 3881470 – QA Specialist

    Responsibilities:   Supports the development and maintenance of quality procedures, and systems related to Primary Manufacturing Quality Assurance oversight. Provides technical support for the US FCC site in all cGMP compliance related matters, including assurance that all aspects comply with cGMPs, legal, regulatory requirements, and the company Quality Manual requirements. Ensures that all aspects of USFCC operations comply with the requirements of the Quality manual and meets all relevant ...

  21. 3881470 – QA Specialist

    Responsibilities: • Supports the development and maintenance of quality procedures, and systems related to Primary Manufacturing Quality Assurance oversight. • Provides technical support for the US FCC site in all cGMP compliance related matters, including assurance that all aspects comply with cGMPs, legal, regulatory requirements, and the company Quality Manual requirements. • Ensures that all aspects of USFCC operations comply with the requirements of the Quality manual and meets all relevant ...