Senior CQV Engineer

Job Title:
Senior CQV Engineer

Duration: 6 months

Join our dynamic team as a Senior CQV Engineer, where you will have the opportunity to make a significant impact in the pharmaceutical manufacturing sector. We are looking for a dedicated professional with 3-10+ years of experience in Commissioning, Qualification, and Validation (CQV) to support our projects.

Your responsibilities will include:

• Developing, executing, and documenting commissioning, qualification, and validation protocols (IQ/OQ/PQ) for new and modified equipment, utilities, and facilities.
• Authoring and reviewing qualification documents, test scripts, deviation reports, and summary reports to ensure compliance and quality.
• Performing risk-based commissioning and qualification activities in alignment with FDA, EMA, and internal quality standards.
• Coordinating closely with engineering, quality assurance, validation, and operations teams throughout the CQV lifecycle for seamless integration.
• Supporting technology transfer, process validation, and the handover to manufacturing to ensure efficient operations.
• Participating in deviation investigations, implementing CAPA, and contributing to the continuous improvement of CQV processes.

If you are passionate about ensuring quality and compliance in pharmaceutical manufacturing, we encourage you to apply and become a vital part of our team.