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QA & QC Operations Lead – GMP Compliance & Lab Oversight

Moderna, Inc.

Milton Keynes

On-site

GBP 55,000 - 75,000

Full time

Yesterday
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Job summary

A leading biotechnology company in Milton Keynes seeks an experienced QA professional to provide strategic quality oversight in QC laboratories. You will play a crucial role in ensuring compliance with regulatory standards while fostering a culture of innovation and continuous improvement. The ideal candidate has over eight years of experience in the Biopharmaceutical industry, excellent leadership skills, and a solid understanding of cGMP regulations. This position offers a competitive salary, comprehensive benefits, and the opportunity to contribute to groundbreaking mRNA technology.

Benefits

Quality healthcare and insurance benefits
Generous paid time off
Free access to fitness and mindfulness classes

Qualifications

  • 8 – 10+ years of experience in the Biopharmaceutical or Pharmaceutical Industry within Quality.
  • Experience with regulatory inspections as a Subject Matter Expert.
  • Strong working knowledge of relevant regulatory guidance documents.

Responsibilities

  • Provide strategic and operational quality oversight to QC laboratories.
  • Lead QA review and approval of laboratory-related documentation.
  • Support continuous GMP compliance and conduct risk-based QA decision-making.

Skills

cGMP regulations
Project management
Leadership
Risk management
Communication

Education

Bachelor's Degree in a scientific field
Job description
A leading biotechnology company in Milton Keynes seeks an experienced QA professional to provide strategic quality oversight in QC laboratories. You will play a crucial role in ensuring compliance with regulatory standards while fostering a culture of innovation and continuous improvement. The ideal candidate has over eight years of experience in the Biopharmaceutical industry, excellent leadership skills, and a solid understanding of cGMP regulations. This position offers a competitive salary, comprehensive benefits, and the opportunity to contribute to groundbreaking mRNA technology.
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