CQV Lead - CIP/COP Systems

Biopharma-Consulting-Jad-Group

Carolina (PR)

On-site

USD 140,000 - 180,000

Full time

3 days ago
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Job summary

Biopharma-Consulting-Jad-Group seeks a senior CQV lead to direct CIP/COP activities for a multi-year pharmaceutical program in Carolina, Puerto Rico. You will set technical direction, guide the team, and drive CQV from startup through qualification.

The role requires 13+ years of CQV experience, subject matter expertise in CIP/COP, and a proven ability to lead the CQV area independently; Bachelor’s degree in Engineering or Life Science is required. On-site, five days a week, starting Jan 4, 2027.

Qualifications

  • 13+ years of pharmaceutical CQV experience.
  • Subject matter expert in CIP/COP: equipment, cleaning processes, system design and C&Q/verification.
  • Proven ability to lead a CQV area independently.
  • Bachelor's degree in Engineering or a Life Science.

Responsibilities

  • Lead CIP/COP commissioning, qualification and verification as area owner.
  • Give technical direction on cleaning processes, system design and cycle development.
  • Coordinate execution with engineering, automation, quality and construction.
  • Support other CQV areas as needed (process equipment, utilities, startup, automation).

Skills

Pharma CQV experience
CIP/COP subject matter expert
CQV area leadership

Education

Bachelor's degree in Engineering or Life Science

Job description

Lead the clean-in-place / clean-out-of-place area of a multi-year greenfield pharmaceutical program in Carolina, Puerto Rico. As the subject matter expert, you will set the technical direction, guide the team and drive CQV from startup through qualification.

What you\'ll do
  • Lead CIP/COP commissioning, qualification and verification as area owner.
  • Give technical direction on cleaning processes, system design and cycle development.
  • Coordinate execution with engineering, automation, quality and construction.
  • Support other CQV areas as needed (process equipment, utilities, startup, automation).
  • 13+ years of pharmaceutical CQV experience.
  • Subject matter expert in CIP/COP: equipment, cleaning processes, system design and C&Q/verification.
  • Proven ability to lead a CQV area independently.
  • Bachelor\'s degree in Engineering or a Life Science.
  • Contract: 60 months (multi-year program), with possible extension
  • Shift: Administrative, Monday–Friday, on-site 5 days/week
  • Start: January 4, 2027
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