Quality Assurance Specialist

​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!