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Job Description

Cpl Life Sciences are partnered with pharmaceutical manufacturer based in Liverpool, recruiting a Process Technician for a 6-month contract position. This is a hands-on role supporting critical manufacturing operations, utilities, and materials handling within a highly regulated GMP environment.

The role operates on a 2 days / 2 nights / 4 off shift pattern and is Inside IR35.

Key Responsibilities

Monitor plant equipment and systems to ensure compliance with environmental, GMP, and safety regulations Complete GMP documentation accurately and in line with regulatory and legislative requirements Maintain high standards of safety, quality, and housekeeping in accordance with site procedures and cGMP expectations Report safety, quality, and compliance issues via incident, near-miss, and deviation reporting systems Work collaboratively within a multi-functional team and liaise cross-functionally to support operational objectives Complete all mandatory training and contribute to continuous improvement activities, including Lean, 5S, and waste reduction initiatives

Role Requirements

Experience working in a chemical, pharmaceutical, or biotechnology manufacturing environment Background in a process or engineering support role Ability to work in a cGMP- and HSE-regulated environment with an understanding of FDA, MHRA, HSE, and Environment Agency requirements Strong written and verbal communication skills Mechanical aptitude with knowledge of electrical and mechanical equipment Ability to follow complex procedures and work effectively under pressure

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