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manufacturing in Raleigh

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  1. Purification Bulk Support

      My name is Paige, and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a candidate for a Purification Bulk Support position for a prominent client of ours.  This position is located in Holly Springs, NC.  Details for the positions are as follows: Will provide technical support for the downstream (purification) portion of the process to the bulk manufacturing team.  Manufacturing on-floor technical support and troubleshooting (off hours as necessary) ...

  2. 3916032-Purification Bulk Support Contractor

    Job Description & Responsibilities The Manufacturing Science and Technology (MS&T) group currently has a position open for manufacturing support of the flu cell culture (FCC) process.  The candidate will provide technical support for the downstream (purification) portion of the process to the bulk manufacturing team.  The successful candidate will perform activities including: Manufacturing on-floor technical support and troubleshooting (off hours as necessary) Deviation investigation and ...

  3. 3838420 – Shop Floor QA Associate

      Responsibilities: ·         Perform batch record review concurrent to completion of manufacturing operations in real time. ·         Perform routine quality audits in Manufacturing. ·         Support quality systems related to QA for in-process sampling and controls, and all aspects of shop floor QA. ·         Act as quality representative on the floor during manufacturing areas. ·         Support the development of SOPs and batch records.   Requirements: ·         Experience in QA ...

  4. EHS Manager-paid relo to Wichita, KS-bza5692RA

    The purpose of the job is to manage and administer the health, safety and environmental programs at the fiber glass manufacturing plant. This position provides operational leadership in areas of injury reduction, hazard mitigation, injury case management, pollution prevention, spill response, emergency preparedness, waste minimization, and overall implementation and management of health, safety and environmental programs. Relationship building with local, state, and federal regulatory agencies and ...

  5. 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 ...

  6. 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 ...

  7. Manager Supplier Quality

    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 a Manager Supplier Quality for our client in the ...

  8. 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 ...

  9. 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 ...

  10. Specialist Mechanical Design Engineer - Medical Devices

    As part of an R&D project team, the specialist engineer owns the design of a complete module or sub-assembly, from conception to design and verification. He/She works at a senior position and ensures that the project progresses in the defined manner. With his/her expert knowledge, the specialist engineer also provides guidance to other engineers on their technical issues, engages in design reviews and help resolves the most complex problems. Essential Duties and Responsibilities: - Acts as an ...

  11. 3879400 – Deviations Investigator

      Responsibilities:   The deviation owner will lead the investigation of deviations that occur in operations and are responsible for authoring the investigation. Partners with quality assurance, quality control, operations, engineering, maintenance, calibration, safety and supplier quality management to ensure appropriate and timely determination of scope, product impact, root cause and corrective actions. Interacts will all levels of staff and provides status updates as well as present the ...

  12. 3877598 - Tech Transfer Scientist/Engineer

    The Manufacturing Science and Technology (MS&T) group currently has a position open for leading of an internal technical transfer/line extension of a flu cell culture (FCC) drug product. The candidate will provide serve as a technical lead for the development of the new drug product process. Responsibilities • Determining critical process parameters and design for the product • Leading the process validation of the product • Writing, executing, reviewing and/or approving technical documents, ...

  13. 3877598 - Tech Transfer Scientist/Engineer

    The Manufacturing Science and Technology (MS&T) group currently has a position open for leading of an internal technical transfer/line extension of a flu cell culture (FCC) drug product.   The candidate will provide serve as a technical lead for the development of the new drug product process.   Responsibilities   Determining critical process parameters and design for the product Leading the process validation of the product Writing, executing, reviewing and/or approving technical documents ...

  14. Quality Assurance - High Level Manager Consultant - Multiple Locations

    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 Quality Assurance or Compliance Engineer ...