Pharma QA Officer β€” GMP & CAPA Compliance (On-Site) in Stafford

Pharma QA Officer β€” GMP & CAPA Compliance (On-Site) in Stafford

Stafford Full-Time 29700 - 36300 Β£ / year (est.) No working from home possible
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At a Glance

  • Tasks: Ensure compliance with GMP and quality systems in a pharmaceutical environment.
  • Company: Join a leading pharmaceutical client dedicated to quality and safety.
  • Benefits: Full-time position with competitive salary and career advancement opportunities.
  • Other info: Collaborative team environment with a focus on professional growth.
  • Why this job: Make a difference in the pharmaceutical industry by ensuring product quality and safety.
  • Qualifications: 2-3 years of QA experience in pharma, preferably with sterile manufacturing knowledge.

The predicted salary is between 29700 - 36300 Β£ per year.

ARx Recruitment Services is seeking an experienced QA Officer to join the Quality Team for a pharmaceutical client in the UK.

The role is full-time and on-site, reporting to the Corporate Senior QA Manager and collaborating with UK QA departments to ensure GMP and company procedures are followed.

The candidate should have 2–3 years of QA experience in pharma, ideally with sterile manufacturing exposure, and a solid understanding of GMP and quality systems.

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Pharma QA Officer β€” GMP & CAPA Compliance (On-Site) in Stafford employer: ARx Recruitment Services

As a Quality Control Technician, you will join a dynamic team dedicated to maintaining the highest standards of quality in our products. Our company fosters a collaborative work culture that values employee input and offers ample opportunities for professional growth and development. Located in a vibrant area, we provide competitive benefits and a supportive environment that makes us an excellent employer for those seeking meaningful and rewarding careers.

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Contact Details:

ARx Recruitment Services Recruitment Team

We think you need these skills to ace Pharma QA Officer β€” GMP & CAPA Compliance (On-Site) in Stafford

GMP Compliance
Quality Assurance
Pharmaceutical Industry Knowledge
Sterile Manufacturing Experience
Quality Systems Understanding
Collaboration Skills
Attention to Detail