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