CQV Project Manager – GMP Validation & Facility Expansions

PSC Biotech® Corporation; Oceanside (CA); On-site; USD 115,000 - 140,000; Full time

Benefits offered by this job

Medical, Dental, Vision

401(k) and matching

Paid time off & holidays

Education Assistance

Pet Insurance

Wellness discounts

Job summary

PSC Biotech® is seeking a highly skilled CQV Project Manager to lead and support validation strategies across the CQV lifecycle for pharmaceutical facilities. You will guide cross-functional teams in planning, execution, and regulatory compliance to ensure quality and timely project delivery.

This role requires a Bachelor's in engineering and 5+ years of end-to-end CQV project experience, with strong budgeting, risk, and vendor coordination skills to drive successful facility expansions and

Qualifications

• Bachelor's degree in related engineering discipline required.
• 5+ years of experience managing end-to-end CQV activities for capital projects.
• Strong in project planning, scheduling, budget management, risk mitigation, and stakeholder communication.

Responsibilities

• Lead and coordinate CQV lifecycle activities for GMP pharmaceutical production environments.
• Provide expert leadership in planning, development, and execution of facility build-outs and expansions.

Job description

PSC Biotech® is seeking a highly skilled CQV Project Manager to lead and support validation strategies across the CQV lifecycle for pharmaceutical facilities. You will guide cross-functional teams in planning, execution, and regulatory compliance to ensure quality and timely project delivery.

This role requires a Bachelor's in engineering and 5+ years of end-to-end CQV project experience, with strong budgeting, risk, and vendor coordination skills to drive successful facility expansions and