I am looking for an experienced Analytical Sciences Manager to oversee the QC analytical team responsible for product release and stability testing. This role will ensure that laboratory operations comply with global regulatory standards, drive continuous improvement, and support audit readiness.
Key Responsibilities
* Lead and manage a QC analytical team, ensuring all testing activities comply with GMP regulations.
* Oversee product release and stability testing, ensuring results are accurate and delivered on time.
* Maintain an inspection-ready QC laboratory and ensure compliance with data integrity guidelines.
* Manage the laboratory schedule to optimize resources and meet business deadlines.
* Investigate quality events, deviations, and out-of-specification (OOS) results, ensuring timely resolution.
* Support the development and validation of analytical methods for routine testing.
* Liaise with external testing laboratories and regulatory agencies as required.
* Ensure all team members are appropriately trained and maintain high documentation standards.
* Contribute to continuous improvement initiatives to enhance quality and efficiency.
What You'll Need
* Significant experience in a QC leadership role within a GMP-regulated biopharmaceutical or pharmaceutical environment.
* Strong understanding of analytical techniques, stability programs, and regulatory guidelines.
* Degree in a relevant scientific discipline.
* Excellent leadership, problem-solving, and technical writing skills.
* Proactive, conscientious, and able to work effectively in a flexible environment.
Why Apply?
* Work with an innovative company at the forefront of biopharmaceutical development.
* Lead a high-performing QC team in a laboratory setting.
* Career progression opportunities.
* Be part of a collaborative and forward-thinking organisation.
How to Apply: If you're ready for your next challenge, apply now!
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