CQV Manager Pharmaceutical Facilities

1 week ago


Columbus, Ohio, United States PSC Biotech Full time

PSC Biotech is seeking a highly skilled CQV Manager Pharmaceutical Facilities to lead our commissioning, qualification, and validation projects. As a key member of our team, you will oversee project planning, CQV execution, and ensure operational readiness of capital projects to support our clients' success.

Responsibilities include driving project success by assessing priorities and project plans, schedule, and budget, ensuring timely and effective resolution of potential risks and issues. You will develop and execute commissioning, qualification, and validation protocols for required equipment and systems, and prepare comprehensive documentation.

This role requires advanced knowledge of regulatory requirements and industry standards, as well as experience with validation lifecycle management and risk-based approaches. You will also serve as liaison between vendors and contractors, coordinating required hand-offs, and ensure compliance with regulatory requirements (FDA, EMA, etc.) and industry standards (GMP, GAMP, etc.).

The estimated salary for this position is $130,000 - $160,000 per year, depending on experience. If you have a Bachelor's degree in engineering or a related field, 10+ years of commissioning, qualification, and validation engineering experience in the pharmaceutical and/or biotech industries, and excellent analytical and technical problem-solving skills, we encourage you to apply.



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