Principal QA Specialist
Posted 2 weeks ago by Hyper Recruitment Solutions
Negotiable
Undetermined
Hybrid
England, United Kingdom
Summary: A leading pharmaceutical company is seeking a Principal Quality Assurance Specialist for their West London team. This role involves ensuring compliance with Good Manufacturing Practices (GMP) and supporting operations through quality management processes. The position is initially fully onsite with potential for hybrid work arrangements. The ideal candidate will have a relevant scientific degree and proven experience in Quality Assurance or Quality Control.
Key Responsibilities:
- Provide review, approval, and support for managing quality records such as Deviations, CAPA, Change Controls, and Investigations.
- Manage and escalate major and critical compliance issues through site Quality Management System (QMS) processes.
- Actively identify, suggest, and participate in continuous improvement activities.
- Mentor and coach business partners in current Good Manufacturing Practices (cGMP) to maintain and develop a quality culture.
Key Skills:
- Relevant degree in a scientific field.
- Proven industry experience in Quality Assurance (QA) or Quality Control (QC).
- A working knowledge and practical experience with managing Deviations, CAPA, Change Controls, and Investigations.
Salary (Rate): undetermined
City: undetermined
Country: United Kingdom
Working Arrangements: hybrid
IR35 Status: undetermined
Seniority Level: undetermined
Industry: Other
Role Overview A leading company in the pharmaceutical industry is seeking a dedicated Principal Quality Assurance Specialist to join their team based in the West London area. This role is initially fully onsite with the possibility of 1-2 days work from home thereafter. As the Quality Assurance Specialist, you will play a crucial role in supporting operations to ensure compliance with Good Manufacturing Practices (GMP).
Key Duties And Responsibilities Your duties as the Quality Assurance Specialist will be varied however the key duties and responsibilities are as follows:
- Provide review, approval, and support to key business partners for managing quality records such as Deviations, CAPA, Change Controls, and Investigations.
- Manage and escalate major and critical compliance issues through site Quality Management System (QMS) processes.
- Actively identify, suggest, and participate in continuous improvement activities.
- Mentor and coach business partners in current Good Manufacturing Practices (cGMP) to maintain and develop a quality culture.
Role Requirements To be successful in your application to this exciting role as the Quality Assurance Specialist, we are looking to identify the following on your profile and past history:
- Relevant degree in a scientific field.
- Proven industry experience in Quality Assurance (QA) or Quality Control (QC).
- A working knowledge and practical experience with managing Deviations, CAPA, Change Controls, and Investigations.
Key Words: Quality Assurance / GMP / Quality Management System / CAPA / Deviations / Change Controls / Continuous Improvement / cGMP / Pharmaceutical / Compliance / Quality Culture
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.