Formulation Technician – GMP Lab Production

Manpower UK

East Grinstead

On-site

GBP 18,000 - 23,000

Full time

13 days ago

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Benefits offered by this job

20% shift allowance

Job summary

Manpower UK in East Grinstead is seeking a temporary Formulation Tech to support production in the laboratory and aseptic dispensing room, producing Sensititre antimicrobial plates. The role is 38 hours per week on a three-week daytime rota, including one weekend in three, with potential to become permanent after six months.

You will prepare media and reagents, uphold GLP/GMP, SOPs, and maintain accurate documentation while collaborating with the production team to ensure quality output.

Qualifications

  • Ideally educated to A-level standard in a scientific subject.
  • Capable of following SOPs and H&S guidelines.
  • Good teamwork and communication skills.
  • Able to organise and prioritise tasks under own initiative.
  • Attention to detail when following procedures and keeping records.

Responsibilities

  • Preparation of antimicrobic solutions per SOPs and production paperwork.
  • Set-up and monitoring of production dispensing pumps for on-time output.
  • Manufacture of ancillary solutions – ID media, buffers and excipients.
  • Compliance checks of laboratory equipment and instrumentation.
  • Maintain and monitor raw material stock levels.
  • Support the laboratory by washing and autoclaving equipment.
  • Utilise SAP ERP, Microsoft Office and bespoke programs for data processing.
  • Additional duties as required by the business.

Skills

GMP environment
Lab experience
Quality minded

Education

A-level science

Tools

SAP ERP
Microsoft Office

Job description

Manpower UK in East Grinstead is seeking a temporary Formulation Tech to support production in the laboratory and aseptic dispensing room, producing Sensititre antimicrobial plates. The role is 38 hours per week on a three-week daytime rota, including one weekend in three, with potential to become permanent after six months.

You will prepare media and reagents, uphold GLP/GMP, SOPs, and maintain accurate documentation while collaborating with the production team to ensure quality output.

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