Quality Assurance Specialist
1 month ago
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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