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