Job Descrption
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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