Quality Assurance Manager, BIO/GLP

Quality Assurance Manager, BIO/GLP
  • $90,000 - $120,000 per Hour
  • Permanent
  • Exton PA, US Exton CHESTER US 19341
Job Ref: JO000124175
Sector: Clinical
Sub-sector: Quality
Date Added: 12 October 2021

Quality Assurance Manager, BIO/GLP

At SRG, we create meaningful connections that empower individuals and businesses to shape tomorrow’s world.

Working as part of the SRG team, you will work with our client which are Pharmaceutical or Bio-Pharmaceutical companies to ensure work quality and accuracy for our client in the Bio Pharmaceutical Industry. The Quality Assurance Manager, BIO/GLP will implement, maintain and enhance quality procedures and systems to ensure compliance with US FDA, OECD, and ICH regulatory requirements including 21 CFR Part 58, 21 CFR Part 11, 21 CFR Part 320, and other relevant guidances and publications.

Role & Responsibilities

  • Assist the Sr. Director with client audits / regulatory inspections and as back-up in their absence
  • Assist with client RFIs and requests
  • Assist the Sr. Director with audit schedules
  • Conduct QA audits of bioanalytical laboratories and functions including but not limited to: ongoing process, data review audits, technical report, and study independent facility / process.
  • Provide input to method, equipment, computer validation programs.
  • Maintain GLP Master Schedule.
  • Maintain appropriately detailed notes, audit reports, and records
  • Provide input to documentation and data storage systems.
  • Ensure that requirements and documentation for all GLP systems are kept current according to ever-changing guidelines and industry standards.
  • Provide GLP training to staff as necessary.
  • Effectively report quality issues to supervisor, Study Director, and Frontage management, as appropriate.
  • Provide oversight and input to analytical and process investigations, CAPA and calibration programs, specifications, and supplier selection processes.
  • Conduct outside vendor audits as may be required, including contract laboratories and raw material suppliers; resolve and follow-through on any quality issues.
  • Review and maintain up-to-date Standard Operating Procedures (SOP).


  • BS in Chemistry, or other related discipline
  • Five (5) years of relevant experience in the pharma industry

SRG is an Equal Opportunity Employer - All qualified applicants will receive consideration without regard to race, color, religion, gender, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law.

27/11/2021 12:00:00
USD 90000.00 120000.00 Hour
Contact Consultant:
Shari Hulitt

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