CQV Lead - CIP/COP Systems

BioPharma Consulting JAD Group

Carolina (PR)

Presencial

USD 120.000 - 180.000

Jornada completa

Hace 12 días

Una candidatura completa en un minuto

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Descripción de la vacante

BioPharma Consulting JAD Group is seeking a senior CQV lead to direct CIP/COP commissioning, qualification, and verification for a multi-year program in Carolina, Puerto Rico. You will set technical direction and guide the team through CQV from startup through qualification on a 5-year contract, on-site five days a week.

The candidate should have 13+ years of pharmaceutical CQV experience and be a subject matter expert in CIP/COP, equipment, cleaning processes, system design and

Formación

  • 13+ years of pharmaceutical CQV experience.
  • Subject matter expert in CIP/COP: equipment, cleaning processes, system design and C&Q/verification.
  • Ability to lead a CQV area independently.

Responsabilidades

  • 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).

Conocimientos

CQV experience
CIP/COP expertise
Leadership
System design
Verification

Educación

Bachelor’s degree in Engineering or Life Science

Descripción del empleo

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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