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QA Manager

Michael Page Engineering & Manufacturing
Job LocationStaffordshire
EducationNot Mentioned
SalarySalary negotiable
IndustryNot Mentioned
Functional AreaNot Mentioned
Job TypePermanent , full-time

Job Description

Youll be QA Manager for a solid-dose pharmaceuticals manufacturing SME, leading a team responsible for general QMS activity. Your team will have eight QA specialists, and youll be tasked with coaching and developing them to ensure they become future starsin the industry, as well as growing your own career by taking on more responsibility.Client DetailsAn SME manufacturer of solid-dose products based in Staffordshire sold in human and veterinary channels. There is a GMP manufacturing & packaging facility on-site, in addition to a GLP accredited laboratory specialising in analytical chemistry to ensurecompliance and high quality products.DescriptionAs the QA Manager, youll be leading a team of QA specialists focusing mostly on core QMS activity and guiding the business through external MHRA and GMP audits.Day to day activities include:

  • External audit management - customers / 3rd parties & regulatory bodies
  • Drive CI culture and best-practice by demonstrating effective RCA processes and know-how
  • Supplier mapping
  • API declarations
  • Continuous development of the QA team - lead by example, coach and develop individuals where required and appropriate
  • Ensure adherence to Health & Safety & GMP
  • Act as subject matter expert in the Quality field, and be a go-to person for troubleshooting and problem solving
ProfileYou dont necessarily have to be working as a QA Manager right now - were happy to consider people who are looking for that next step, but youll need to have experience leading a team, delegating tasks and strong interpersonal skills.Youll have a sound grasp of whats necessary in a GMP manufacturing facility, and have specific pharmaceuticals knowledge. Product knowledge isnt important, its more about understanding what it takes to ensure compliance in this type of manufacturingoperation.Most importantly, we need a people person. Somebody who is able to interact with the team effectively - coaching and developing them along the way whilst ensuring the highest standards of quality are upheld.Depending on your experience, there is an option for somebody to take on a more senior QA Manager role, encompassing elements of non-predictable quality such as NCRs, complaints, deviations and CAPAs.Essentially, were able to tailor this position to ensure you succeed.Job Offer
  • Salary negotiable depending on experience.
  • Monday to Friday - 37.5 Hours worked between 7am and 5pm. Hours can be flexible and discussed.
  • Private Healthcare.
  • Pension.
For further information please contact Natalie Hudson at Michael Page Birmingham.

Keyskills :
GMPcompliancepharmaceuticalquality assurancevalidation

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