Senior Process Quality Excellence Specialist
Posted 2 weeks ago by Warman O'Brien
Negotiable
Undetermined
Undetermined
Slough, England, United Kingdom
Summary: The Senior Process Quality Excellence Specialist will play a crucial role in supporting the Head of Process Quality Excellence by developing and maintaining clinical quality systems and ensuring compliance with relevant regulations. The position requires extensive experience in Good Clinical Practice, Good Laboratory Practices, and Pharmacovigilance. The specialist will collaborate with various stakeholders to ensure inspection readiness and lead activities related to quality and compliance. This role is based in Slough, England, and is offered as a 12-month contract.
Key Responsibilities:
- Support the Head of Process Quality Excellence in quality and compliance infrastructure development.
- Assist with creation/revision of quality and compliance policies, Standard Operating Procedures, and best practices.
- Collaborate with Global Quality, Patient Safety, Regulatory Affairs, and other stakeholders to ensure compliance with ICH GCP, GLP, PV, and relevant regulations.
- Lead and drive Inspection Readiness Activities across all functions.
- Participate in Audit and Inspection planning with Global Quality.
- Represent or ensure representation during audits/inspections and support staff with audit/inspection responses.
Key Skills:
- 8+ years of pharmaceutical experience, preferably in Quality Assurance or Clinical Development.
- In-depth experience of GCP and GVP, including hands-on experience in global GCP audits and/or inspections.
- 2+ years of experience in SOP writing.
Salary (Rate): undetermined
City: Slough
Country: United Kingdom
Working Arrangements: undetermined
IR35 Status: undetermined
Seniority Level: undetermined
Industry: Other
Senior Process Quality Excellence Specialist 12 month contract Global Pharma The Senior Process Quality Excellence Specialist will support the Head of Process Quality Excellence in developing and maintaining its clinical quality systems/procedures and ensuring quality and compliance risks are appropriately identified and mitigated. Applicants must have comprehensive experience in Good Clinical Practice, Good Laboratory Practices and Pharmacovigilance regulations and guidance.
Responsibilities: Support the Head of Process Quality Excellence in quality and compliance infrastructure development; assist with creation/revision of appropriate quality and compliance policies, Standard Operating Procedures, processes, and best practices as needed. Work in collaboration with Global Quality, Patient Safety, Regulatory Affairs, strategic partners, and other stakeholders to ensure compliance with International Council for Harmonization of Technical Requirements for Pharmaceutical for Human Use (ICH) GCP, GLP, PV and relevant local and international regulations and to ensure inspection readiness. Lead and drive Inspection Readiness Activities across all functions working closely with the relevant inspection teams. Participate in Audit and Inspection planning with Global Quality. Represent or ensure representation including preparation during audits/inspections. Support staff with audit/inspection responses, where required.
Requirements: 8+ years of pharmaceutical experience, preferably in a global Quality Assurance or a Clinical Development setting. In depth experience of GCP and GVP, including hands on experience in global GCP audits and/or inspections. 2+ years of experience in SOP writing essential. For additional information, and a confidential discussion, please apply now with an updated CV.