Manager, Manufacturing Compliance - Pharmaceutical

Paragon Bioservices   •  

Harmans, MD

Industry: Pharmaceuticals & Biotech

  •  

8 - 10 years

Posted 171 days ago

This job is no longer available.

Paragon Bioservices, Inc. (PBI) is a growing Biotech Contract Development and Manufacturing Organization (CDMO) with an internationally recognized tradition of quality and service. Paragon Bioservices provides process development and GMP manufacturing services for Phase I/II clinical trials to industry leaders as well as innovative start-ups utilizing novel technologies to produce state-of-the-art vaccines and therapies for people when they are most in need. As a PBI employee, you will actively contribute to the delivery of our services and products to our customers and their patients.

The Manufacturing Compliance Manager manage the compliance function within Manufacturing and is responsible for the batch records lifecycle throughout the manufacturing plant. Once documents have been created and approved, the incumbent will be responsible for tracking the lifecycle of batch records and documents to support manufacturing activities. This position also writes and reviews standard operating procedures (SOPs).

Key Responsibilities:

  • Management of the compliance function and team for GMP manufacturing compliance
  • Responsible for ensuring documentation including batch records, SOPs, logbooks, etc. that will be used throughout the manufacturing facility
  • Adheres to internal/external guidelines, specifications, and regulatory requirements while creating and maintaining documentation
  • Ensures that SOPs relevant to documentation (batch records, logbooks, etc.) are generated, maintained and available
  • Tracks GMP review and production close out of batch record documentation
  • Key contact with Quality Assurance to ensure robust and stable document flow from issuance to archiving
  • Positively interacts with internal associates to quickly and effectively resolve issues
  • Addresses deficiencies and ensures completion of all follow-up actions, specifically those that target process fixes to maintain consistent resolutions to all batch review issues according to GMP standards and company objectives
  • Supports implementation of CAPAs, SOP revisions, quality improvement initiatives, operational excellence projects, etc.
  • Develops processes for batch records including for issuing, tracking and reviewing batch records
  • Develops and maintains metrics to track batch record turnaround time, errors and document related deviations

Education / Experience:

  • Bachelor’s degree in Chemistry, Life Science or Engineering field
  • 8+ years of broad cGMP production experience, with knowledge and understanding of process, documentation requirements and activities, preferably in an biologics manufacturing environment
  • 3 years in a leadership role
  • Extensive experience with GMP documentation management

 Requisition ID : 1124