QC SAMPLE COORDINATOR l

PCI Pharma ServicesBedford, NH
1d

About The Position

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI. JOB DESCRIPTION: Position Title : QC Sample Coordinator I Location: Bedford, New Hampshire Department: Quality Control / Incoming materials Reporting To: QC Supervisor, Sample Management Responsible For (Staff): No This position will have responsibility for supporting activities in the QC Sample Management group, which includes use of material control procedures and specification documents, raw material sampling & inspection, participation in the coordination of testing with internal and external resources, and collection of data and material certificates for review by QA.

Requirements

  • 1-3 years relevant business experience
  • Proficient in MS Office.
  • Must have strong attention to detail as well as ability to work in a cross-functional team environment
  • Professional interpersonal skills and the ability to communicate well orally and in writing
  • Ability to multi-task in a dynamic environment with changing priorities

Nice To Haves

  • Ability to work independently as well as on a team, with limited supervisory oversight
  • Master Control experience a plus
  • cGMP experience a plus

Responsibilities

  • Ordering, receipt and management of QC Laboratory supplies, including chemicals, reference standards, and consumable materials in accordance with cGMP and procedural requirements
  • Inspection, review and receipt of incoming samples for testing. Verification of information against specifications, protocols, and other documentation to ensure compliance.
  • Maintain sample tracking and chain of custody records in accordance with cGMP and procedural requirements
  • Complete data entry in validated systems and business tools with a high degree of accuracy.
  • Request, assemble, and distribute QC testing data packets for support of in-process, lot release, raw material, and stability testing
  • Assist with coordinating external testing
  • Request and maintain Quality Control logbooks in accordance with cGMP and procedural requirements
  • Perform inspections on packaging components
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