Role
Contract Length: 12 Months. Location: Primarily on-site. Working Hours: Standard business hours, with flexibility required to support project activities and key milestones.
Desirable Experience
Laboratory systems qualification
Autoclave qualification an advantage
Clean utilities commissioning and qualification (e.g., PW, WFI, Clean Steam, Process Gases)
Experience working on CAPEX projects within GMP-regulated environments
Required Experience & Qualifications
Degree or equivalent qualification in Engineering, Life Sciences, or a related technical discipline
Experience in a C&Q, Validation, or Engineering role within the pharmaceutical, biotechnology, or regulated manufacturing industry
Strong knowledge of GMP and qualification lifecycle activities
Experience with manufacturing equipment, utilities, facilities, or laboratory systems qualification
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