Senior QC Project Manager
2 weeks ago
Dechra Pharmaceuticals PLC is seeking a highly skilled Senior QC Project Manager to lead our Quality Control project team. The successful candidate will be responsible for optimizing test regimes on products, working in a 24-month fixed-term contract.
About the Role- Lead a team to deliver project objectives to expected timelines.
- Coach and mentor team members to develop relevant skill sets.
- Review specifications to ensure non-value adding tests are removed from the finished product specification.
The ideal candidate will have a strong background in method development in a pharmaceutical GMP environment, with a minimum of 3 years' experience. A HNC/D level in a relevant scientific subject or significant job-specific experience is required.
Salary and BenefitsWe offer a competitive salary of £60,000 per annum, plus benefits including:
- Average 36-hour working week (with a day off every other Friday).
- 5 days annual leave + Bank holidays.
- Option to buy a week's holiday each year.
- 8% Employer Pension Contribution.
- Free access to the Headspace App.
- Employee Assistance Programme.
- On-site parking.
- Volunteering days.
- Company events.
The Senior QC Project Manager will be responsible for:
- Redesigning tests to run more efficiently, better supporting the testing of high numbers of samples at one time.
- Writing development protocols and reports.
- Performing validation and verification, including producing protocols and reports.
- Submitting updated test regimes to regulatory authorities including justification of specification.
- Managing updates to methods, specifications, and test records in Quality Control.
- Utilizing technical knowledge to train and coach project analysts to enable them to support the project goals.
- Liaising with MS&T, QC Support, Regulatory, and QA.
- Acting as subject matter expert in QC for Method Development in HPLC, UPLC, UV, Dissolution, Disintegration, Friability, Hardness, Loss on Drying, FTIR, Karl Fisher, and pH.
- Authoring Risk Assessments for processes, procedures, and systems to ensure risks are identified and appropriately managed.
- Enhancing practices and promoting a culture which is consistent with cGMP, cGLP, and Health & Safety within a pharmaceutical laboratory environment.
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