Quality Control Supervisor

RBW Consulting

Woking

On-site

GBP 35,000 - 50,000

Full time

14 days+

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Job summary

A pharmaceutical consultancy is seeking a hands-on QC Supervisor to manage a laboratory team and oversee daily operations. Candidates should have extensive QC experience within a GMP environment, along with skills in troubleshooting and team management. This role offers significant development opportunities as the company expands. Experience with HPLC and GC is preferred, and the ability to work shifts is required.

Qualifications

  • Proven experience in QC roles within a GMP environment.
  • Strong leadership skills, preferably with team management experience.
  • Ability to work shifts as required.

Responsibilities

  • Lead and manage a team of QC personnel.
  • Oversee daily laboratory operations and troubleshooting.
  • Support the QC documentation process.

Skills

Experienced QC professional within a pharmaceutical GMP capacity
Track record in running a laboratory
Management and workload organization skills
Troubleshooting abilities
HPLC and GC experience
People management experience

Job description

We are delighted to be exclusively supporting a long-standing client with the hire of a brand new QC Supervisor position to support the ongoing expansion and growth of one their key facilities in the South-East of the UK.

This position will be a hands on QC Chemist, taking a lead on running a range of tests and running the laboratory. It will be key to manage staff shift rotas, support technical issues, troubleshoot equipment and support the QC documentation process for the site.

This is an excellent opportunity for an experience QC chemist who has either managed a small team or potential coached and mentored more junior members for some time, performing at a similar level. Given the expansion of the business, the scope for development is significant.

For further information, please contact Mark Bux-Ryan.

The ability to work shifts is necessary.

Key experience
  • Experienced QC professional within a pharmaceutical GMP capacity
  • Track record and experience in day to day running of a laboratory
  • Managing rotas and workload management
  • Troubleshooting and supporting a team with day-to-day issues
  • Experience within HPLC and GC would be strongly preferred
  • People management experience including recruiting and selecting teams
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