At a Glance
- Tasks: Ensure quality oversight in a regulated GMP environment and review batch documentation.
- Company: Join Moderna's innovative team in Harwell, a leader in biotechnology.
- Benefits: Night shift premium, competitive salary, and opportunities for professional growth.
- Other info: Collaborative environment with a focus on continuous improvement and innovation.
- Why this job: Play a crucial role in ensuring product quality and safety in a dynamic industry.
- Qualifications: Experience in QA and knowledge of GMP regulations are essential.
The predicted salary is between 35000 - 45000 £ per year.
Moderna's INT manufacturing team in Harwell seeks a QA professional to provide independent quality oversight in a highly regulated GMP environment.
You will review batch documentation, guide on-the-floor activities, and collaborate across Manufacturing, Quality Control, and Facilities to resolve issues, ensuring deviations and CAPAs are handled promptly.
The role includes authoring SOPs and supporting audits.
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GMP Quality Specialist – On-Floor QA (Night Shift) employer: Initial Therapeutics, Inc.
Initial Therapeutics, Inc. is an exceptional employer located in Harwell, offering a dynamic work environment that fosters collaboration and innovation in the field of immunoassays. With a strong commitment to employee growth, competitive benefits including healthcare and family support, and a culture that values diversity and equal opportunity, this role provides a meaningful opportunity for those looking to make a significant impact in clinical trials.
Contact Details:
Initial Therapeutics, Inc. Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land GMP Quality Specialist – On-Floor QA (Night Shift)
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We think you need these skills to ace GMP Quality Specialist – On-Floor QA (Night Shift)
Some tips for your application 🫡
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Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Initial Therapeutics, Inc. that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
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