We are looking for a Flexi Cleaning Validation Analyst to join a fast-paced pharmaceutical manufacturing environment. This is a 12-month contract, fully onsite, with a rotating 12-hour shift pattern (4 on / 4 off, 07:00–19:00).
Key Responsibilities:
* Swab production equipment and analyze samples in line with GMP and GLP procedures.
* Support cleaning validation activities alongside a trained scientist.
* Use laboratory techniques including balances, pH meters, and HPLC.
* Maintain high-quality documentation and compliance with controlled procedures.
* Keep laboratory areas organized according to 5S principles and follow safety standards (EH&S, COSHH).
* Complete allocated tasks accurately and on time, maintaining a high Right First Time standard.
What We’re Looking For:
* Willingness to work onsite in both lab and manufacturing environments.
* Ability to follow written instructions and protocols precisely.
* Basic knowledge of corporate standards, site policies, and safety procedures.
* Attention to detail and strong commitment to quality and compliance.
* No prior experience required – full training will be provided.
Contract Details:
* Start: ASAP
* Length: 12 months
* Shifts: 12-hour shifts, 4 on / 4 off (07:00–19:00)