Quality Assurance Specialist

1 week ago


London, UK, United Kingdom RBW Consulting Full time

Quality Assurance Specialist – East London


Are you passionate about ensuring the highest standards in pharmaceutical quality? Join this growing team as a Quality Assurance Specialist, where you’ll play a crucial role in administering, monitoring, and completing the Pharmaceutical Quality System. Your expertise will help this pharmaceutical business maintain compliance and excellence in all their procedures.


Key Responsibilities and Accountabilities:

  • Technical Quality Support: Provide support for Analytical Services, including the review and approval of:
  • Analytical Method Development/Verification Protocols and Reports
  • Client Supplied Methods and Specifications
  • Test Data, Calculations, Results, and Certificates of Analysis
  • Equipment Maintenance and Qualification
  • Temperature Data
  • Approved Supplier List
  • Compliance and Investigations: Support investigations, review and approve Deviations, Out of Specifications results, and Requests for Change, ensuring GMP conformance and regulatory compliance.
  • Audits and Reviews: Conduct self-inspection audits, maintain site metrics, and present Quality Management Reviews. Assist in external inspections and support the QA Director.
  • Quality Improvements: Review non-compliance issues, use professional judgment to make quality decisions, and initiate improvements to prevent recurrence.


Person Specification


Personal Attributes:

  • Team Player: Able to manage different stakeholders and policy processes.
  • Flexible: Capable of juggling demands and managing competing priorities.
  • Self-Motivated: Work independently on key responsibilities under the supervision of the Quality Director.
  • Consistent: Uphold high standards in Pharmaceutical Quality Assurance and strive for excellence and efficiency.
  • Problem Solver: Assist team members in identifying and eliminating problems, and train others in quality system procedures.
  • Respected Leader: Command respect from peers and co-workers, uphold company values, and influence others to support quality initiatives.

Safety:

  • Adhere to Company SOPs, Health & Safety, GMP, and other regulatory guidelines.
  • Report near misses and contribute to improving the safety culture.

Knowledge and Skills:

  • Education: Degree level or relevant industry experience in Pharmaceutical Science.
  • Experience: Regulatory audits, working in a regulated environment, and project management.
  • Professional Development: Evidence of continued professional development.


Join our client’s team in Barking and be a part of a company that values quality, safety, and continuous improvement. Apply now to make a significant impact in the pharmaceutical industry



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