Your role will be responsible for ensuring that the commisioning of process equipment and suporting utilites is carried out to site standards.

Within this role you will:

• Assist in the creation and maintenance of equipmet SOPs & Forms
• Generation of commissioning test plans.
• Ensure a high standard of cGMP documentation and that is compliant with regulations
• Supervision of commissioning test teams in the execution of commissioning plans.
• Generation of final reports
• Handover of systems and GMP documentation to Validation department.
• Walk down of systems to ensure system is complete and as per red lined P&ID before formal IQ.

To be successful in this role you will require:

Technical qualification in Electrical, Instrument, Mechanical, Chemical or similar engineering qualification.

Min of 3 years of relevant work experience in a Start up/ Commissioning role in pharmaceutical industry.

Experience of sterile manufacturing within the pharmaceutical industry would be a decided advantage

Knowledge of GMP, safety and environmental regulatory requirements