Type: Contract (12 months) | Shift-based
Responsibilities:
* Operate high-speed manufacturing and packaging equipment in compliance with GMP, safety, and quality standards.
* Perform equipment setup, calibration, cleaning, and routine maintenance to ensure optimal performance.
* Complete batch documentation, SAP process orders, and support change control and deviation processes.
* Conduct in-process testing, sampling, inspections, and contribute to quality investigations (CAPAs).
* Collaborate with cross-functional teams including QA, Engineering, Planning, and Warehouse to meet production targets.
* Participate in equipment qualification (IQ/OQ/PQ), validation, and continuous improvement projects.
Qualifications:
* Previous experience working in a GMP-regulated manufacturing or packaging environment.
* Familiarity with equipment operation and documentation standards.
* Strong attention to detail and the ability to follow procedures accurately.
Full time role working on shifts which alternate every week.
* Shift 1: 6am-14:00 Mon to Fri
* Shift 2: 14:00-20:00 Mon to Fri
Seniority level
* Seniority level
Associate
Employment type
* Employment type
Contract
Job function
* Job function
Manufacturing and Production
* Industries
Pharmaceutical Manufacturing and Biotechnology Research
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