Back to searchAssociate Principal QA Specialist
Hyper Recruitment Solutions LTD
Posted 2 days ago, valid for a month
Windsor, Berkshire SL4, England
£35 - £43 per hour
Full Time
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Sonic Summary
- An esteemed pharmaceutical company is seeking an Associate Principal QA Specialist in the Berkshire area.
- The role requires extensive industry experience in quality assurance within a GMP environment, along with a relevant degree in a scientific discipline.
- Key responsibilities include managing GMP issues, supporting quality records, and mentoring business partners in cGMP practices.
- The position offers a salary of £50,000 to £60,000 and allows for fully onsite work initially, with potential for remote work afterward.
- This is a 12-month contract with the possibility of extension.
This is an initial 12 months, with possible extension.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Associate Principal QA Specialist will be varied; however, the key duties and responsibilities are as follows:
1.As the Associate Principal QA Specialist, you will provide shoulder-to-shoulder review, approval, and support to key business partners for managing quality records such as Deviations, CAPA, Change Controls, and Investigations.
2. As the Associate Principal QA Specialist, you willutilize knowledge of GMP and quality processes to manage and escalate major and critical compliance issues through site QMS processes.
3. As the Associate Principal QA Specialist, you willactively identify, suggest, and participate in continuous improvement activities.
4. As the Associate Principal QA Specialist, you willmentor and coach business partners in cGMP practices to maintain and develop a cGMP environment and quality culture.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Associate Principal QA Specialist, we are looking to identify the following on your profile and past history:
1. Relevant degree in a scientific discipline.
2. Extensive industry experience in quality assurance within a GMP environment.
3. A working knowledge and practical experience with managing quality records, including Deviations, CAPA, Change Controls, and Investigations.
Key Words: Associate Principal QA Specialist / GMP Compliance / Quality Assurance / QMS Processes / Continuous Improvement / cGMP Practices / Quality Records / Deviations / CAPA / Change Controls / Investigations
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.
