Your role will be responsible for ensuring that process equipment is qualified to meet corporate and regulatory standards.

Within this role you will:

• Generation of Equipment Protocols IQ,OQ & PQ.
• Involvement in Pre Qualification activities - Process Equipment/Utilities walkdowns, Commissioning, Documentation reviews.
• Ensure high standard of cGMP documentation ensuring compliance with regulations and corporate standards.
• Construction Dossier/Equipment Data Book reviews.
• Execution of Qualification Protocols.
• Generation of Final Reports.

To be successful in this role you will require:

Technical qualifications in Engineering Discipline

Min of 3 years of relevant work experience in a pharmaceutical Start Up/ Commissioning/ Validation environment.

Knowledge of GMP, safety and environmental regulatory requirements