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