Key Responsibilities:

• Support commissioning, qualification, and validation (CQV) activities for equipment, utilities, and facilities within a GMP-regulated environment.
• Generate, review, and execute CQV lifecycle documents, including Commissioning Protocols, IQ, OQ, and related qualification reports.
• Perform field execution activities, protocol testing, documentation review, and discrepancy resolution.
• Coordinate with engineering, operations, quality, and project teams to ensure timely project delivery.
• Ensure all qualification activities comply with GMP, safety, and company procedures.
• Support project commissioning, start-up, and validation activities during critical project phases.

Requirements:

• Degree in Engineering or related discipline.
• 2–3 years of CQV, Validation, or Commissioning experience within pharmaceutical, biotech, or life sciences industries.
• Strong experience in CQV lifecycle document generation and execution.
• Familiar with GMP documentation practices, IQ/OQ protocols, deviations, and qualification reports.
• Able to work overtime and weekends, including short-notice support during project execution and commissioning phases.
• Good communication skills and ability to work in a fast-paced project environment.