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: ASAPLength: 12 monthsShifts: 12-hour shifts, 4 on / 4 off (07:00–19:00)