CQV Project Manager: GMP Validation & Facility Expansion

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

Benefits offered by this job

Medical, Dental, and Vision insurance

401(k) and matching

PTO, Sick Time, Holidays

Education Assistance

Pet Insurance

Anytime Fitness discounts

Financial perks and discounts

Job summary

PSC Biotech® Corporation is seeking a highly skilled CQV Project Manager to lead validation strategies for GMP pharmaceutical environments. You will oversee facilities expansion, budgeting, and cross-functional collaboration to ensure compliant, on-time delivery of capital projects.

Requirements include a Bachelor's in a related engineering discipline and 5+ years of CQV lifecycle experience. Must be authorized to work in the United States; C2C is not allowed.

Qualifications

• 5+ years of experience managing end-to-end CQV activities for capital projects.
• URS development, FAT/SAT execution, and validation documentation for GMP environments.
• Experience supporting facility expansions and upgrades.
• Full CQV lifecycle project management with planning, scheduling, and budgeting.

Responsibilities

• Lead CQV projects across all lifecycle phases for manufacturing facilities.
• Develop robust validation strategies ensuring regulatory compliance.
• Coordinate cross-functional teams, vendors, and contractors.
• Ensure quality, safety, and project milestones are met.

Skills

CQV project management

Regulatory compliance

Project planning

Budget management

Stakeholder communication

Risk mitigation

Vendor coordination

Leadership

Analytical skills

Problem solving

Education

Bachelor's degree in related engineering discipline

Job description

PSC Biotech® Corporation is seeking a highly skilled CQV Project Manager to lead validation strategies for GMP pharmaceutical environments. You will oversee facilities expansion, budgeting, and cross-functional collaboration to ensure compliant, on-time delivery of capital projects.

Requirements include a Bachelor's in a related engineering discipline and 5+ years of CQV lifecycle experience. Must be authorized to work in the United States; C2C is not allowed.