Quality Assurance

Connecticut  ‐ Onsite
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Description

Role Description:
  • This Quality position is considered a global role reporting into the supplier management team within PharmSci QA who is responsible for supporting the Pharmaceutical Sciences R&D organization.
  • The colleague will assist staff in managing supply chain security and performance of external parties who provide materials for GMP manufacturing.
Responsibilities:
  • Perform a range of duties within the PharmSci 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 network.
Specific Activities May Include:
  • 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 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
  • Provides support to External Party Quality Assurance (EPQA) supplier management program.
  • Meet GMP requirements for oversight of suppliers and material supply channels and provide support of program enhancements
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
  • Supplier Management
  • Supplier Quality
  • Ability to Follow-up
  • Ability to meet deadlines
  • Ability to Work Independently
  • Advanced Communication Skills
  • Detail oriented
  • Oral and Written Communication Skills
  • Project Management
Start date
n.a
From
Synectics
Published at
04.05.2016
Project ID:
1123106
Contract type
Freelance
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