At a Glance
- Tasks: Lead QA interactions and prepare for regulatory inspections in a dynamic environment.
- Company: Join a leading organisation focused on governance and regulatory compliance.
- Benefits: Competitive salary, professional development, and a supportive team culture.
- Other info: 12-month fixed-term contract with opportunities for career advancement.
- Why this job: Make a real impact in ensuring quality and compliance in clinical projects.
- Qualifications: 5–10 years of clinical QA experience with strong governance knowledge.
The predicted salary is between 37800 - 46200 £ per year.
Jas Gujral is seeking a QA Specialist - Project Support for a 12-month fixed-term contract in Stevenage.
The role requires 5–10 years of clinical QA experience, with focus on governance, regulatory readiness, and expansion projects.
You will collaborate with regulatory authorities, clients, and contractors to keep QA processes aligned with GMP expectations.
Key duties include leading QA interactions, regulatory inspections preparation, and maintaining PQS for a multi-client facility while
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QA Specialist – GMP & Regulatory Compliance (12-month FTC) in Stevenage employer: Jas Gujral
Join a forward-thinking technology company that values innovation and collaboration, offering a dynamic work culture where your contributions truly matter. With flexible working arrangements and opportunities for professional growth, particularly in cutting-edge areas like Azure and DevOps, this role in Victoria London provides a unique chance to work on impactful projects alongside talented professionals. Embrace the opportunity to advance your career in a supportive environment that prioritises employee development and well-being.
