Senior QC Project Manager

2 weeks ago


Skipton, North Yorkshire, United Kingdom Dechra Pharmaceuticals PLC Full time
Job Overview

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 Benefits

We 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.
Key Responsibilities

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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