CQV Regional Leader — Life Sciences Projects

IPS-Integrated Project Services; Burlington (MA); On-site; USD 142,000 - 189,000; Full time

Job summary

IPS-Integrated Project Services is seeking a CQV Regional Manager to lead commissioning, qualification, and validation efforts for the life sciences sector in the Burlington, MA area. You will oversee client engagements, budgets, schedules, and staffing for compliance projects across the region.

The role requires 10–15 years of GMP/Validation experience, a Bachelor’s degree in Engineering, and the ability to travel up to 50%.

Qualifications

• Bachelor’s degree in Engineering or related discipline.
• 10–15 years of experience in Pharmaceutical, Biotech, Medical Device Design, Construction, Commissioning, Validation, or QA.
• Experience with GMP/Validation and writing and execution of PFC, FC, IQ, OQ, and PQ forms and protocols for GMP Utilities, Equipment, Systems, and Software.
• Detailed experience in GMP/Validation with knowledge of pharmaceutical Design/Build/Commission/Validate processes and regulatory requirements (FDA, EU and ISPE/ICH).
• Demonstrated expertise by industry (Sterile, OSD, Biotech, Medical Device) or by validation activity (process, cleaning, CSV, methods).

Responsibilities

• Directly responsible for the successful delivery of compliance projects in the designated region.
• Oversee project budgets, schedules, deliverables, quality, and client satisfaction.
• Lead compliance service activities and supervise region-specific compliance projects.
• Support business development strategies and activities, including client engagement.
• Travel up to 50% and manage staff assignments and performance reviews.

Education

Bachelor’s degree in Engineering or related discipline

Job description

IPS-Integrated Project Services is seeking a CQV Regional Manager to lead commissioning, qualification, and validation efforts for the life sciences sector in the Burlington, MA area. You will oversee client engagements, budgets, schedules, and staffing for compliance projects across the region.

The role requires 10–15 years of GMP/Validation experience, a Bachelor’s degree in Engineering, and the ability to travel up to 50%.