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Associate QA Manager

RBW Consulting
Posted a day ago, valid for a month
Location

Stoke-On-Trent, Staffordshire ST41AA, England

Salary

£30,000 - £36,000 per annum

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Contract type

Full Time

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Sonic Summary

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  • The position is for an Associate QA Manager in the pharmaceutical industry, requiring over 5 years of experience in a GMP environment.
  • The role involves managing a small team while remaining hands-on with quality assurance activities.
  • Candidates should have experience in QMS oversight and auditing, with lead auditor experience being advantageous.
  • The company is expanding its Quality team and offers an opportunity for growth into a management position.
  • The salary for this role is competitive and commensurate with experience.

Associate QA Manager

Are you an experienced Senior QA professional looking to step into a leadership role?

Do you enjoy working in a flat structured setting where remaining hands on is essential?

If the answer is yes to these, then this could be your next career move.

We are partnered with a business that we have supported in building out its Quality team structure over the past 18 months. Given an increased demand on the product and further plans for the business to expand, they are now seeking a brand new QA Manager for one their UK facilities.

This is an outstanding opportunity for someone that has established, broad, quality assurance experience, across both operational and systems focused activities. Given that the team size is only small, there is an opportunity for the right person to step into this management position.

Therefore, if you enjoy coaching and mentoring and want to make a more official step into management, please apply.

Please contact Mark Bux-Ryan for further details.

Key experience:

  • Experienced within a pharmaceutical QA position, working in a GMP environment. Ideally upwards of 5 years.
  • Experience of sterile manufacturing is an advantage, but not essential
  • A desire to manage a small team, ideally supported with some previous supervisory or coaching/mentoring experience
  • Strong hands on experience of a range of quality activities, especially in relation to QMS oversight
  • Auditing experience desirable – if you have been a lead auditor, this would be advantageous
  • Knowledge and experience of validation activities

Quality, assurance, qa, GMP, manufacturing, pharmaceutical, QMS, system, operational, manager, supervisor, team, leader, specialist, compliance, regulatory, audit, lead, complaints

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