Quality Assurance

Integrated Resources, Inc
  • Groton, Connecticut
  • Contractor
  • Quick Apply
30 days ago

Job Description

Quality Assurance

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Description

Job Responsibilities:

  • Perform a range of duties within the Pharm Sci QA group, associated with oversight and support of the supplier program (and may also support the external vendor inventory management function)
  • Support efforts to introduce enhancements to the supplier program
  • Responsible for regular communication of quality status and escalation of supplier-related quality issues, maintaining a close working relationship with Inventory Management, PharmSci QA and other sites across the Clients network.
  • Review supplier documentation to support the creation of material supply channels and ensure supply chain security
  • Interface with Inventory Management Personnel to obtain supply chain documentation
  • Collect data to support completion of risk-based supplier assessments
  • Interface with Clients MSQA group to provide updated supplier information
  • Update supplier tracking spreadsheets
  • Research existing supplier audit reports and audit notices
  • Execute QA review and release of routine and high priority transfer/shipment requests and packaging and ancillary components
  • Execute extension of expiry dating
  • Point of Contact for assessment of shipment damage
  • Responsibilities may include occasional special project work and other duties as assigned by the department lead or site leadership.

Qualifications

Qualifications:

  • Minimum BS Degree or equivalent in a scientific discipline.
  • Knowledge of cGMP, including regulations related to supplier management programs is desirable
  • Prior quality assurance experience supporting supplier management is desirable.
  • Experience using SMS, M3, QTS, PDOCS and GDMS is desirable.
  • Solid understanding of cGMPs as they relate to assigned tasks
  • Professional demeanor exhibited through the proficient use of email and phone etiquette
  • Ability to shift priorities and tasks throughout the workday to meet business requirements

Kind Regards

Nishit Malakar

Technical Recruiter

Integrated Resources, Inc.

Numbers & Facts

LocationGroton, Connecticut
Job TypeContractor

Skills

  • Biotech and Pharmaceuticalunmatched
  • Clinical Researchunmatched
  • Current Good Manufacturing Practice (cGMP)unmatched
  • Customer Relationsunmatched
  • Data Collectionunmatched
  • Documentationunmatched
  • Information Technology & Information Systemsunmatched
  • Inventory Managementunmatched
  • Leadershipunmatched
  • Order Picking/Packingunmatched
  • Purchasing/Procurementunmatched
  • Quality Assuranceunmatched
  • Regulationsunmatched
  • Rehabilitation Nursingunmatched
  • Riskunmatched
  • Short Messaging Service (SMS)unmatched
  • Spreadsheetsunmatched
  • Supply Chainunmatched
  • Support Documentationunmatched
  • Technical Recruitingunmatched
  • Vendor/Supplier Evaluationunmatched
  • Vendor/Supplier Managementunmatched

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