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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.
Job Responsibility:
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
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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