Biopharma CQV Engineer for GMP Startup & Utilities

Intellectt Inc

Irvine (CA)

On-site

USD 90,000 - 120,000

Full time

14 days+
Application generator

Stand out for this role — generate a tailored resume and cover letter in about a minute.

Get past ATS filters

Job summary

Intellectt Inc is looking for experienced CQV Engineers for a large-scale greenfield biopharmaceutical manufacturing project located in North Carolina. The role involves executing commissioning, qualification, and startup activities for GMP manufacturing equipment and supporting critical utilities like WFI and HVAC. Ideal candidates should have over 5 years in CQV/Startup within the pharmaceutical industry and possess strong documentation skills. The environment is dynamic, and engineers are expected to drive project timelines effectively.

Qualifications

  • 5+ years of CQV/Startup experience in pharmaceutical, biotech, or life sciences industries.
  • Strong experience in greenfield facility projects.
  • Ability to independently execute qualification and startup activities.

Responsibilities

  • Execute commissioning, qualification, and startup activities for GMP manufacturing equipment.
  • Develop and execute IQ/OQ protocols and commissioning test plans.
  • Support startup and troubleshooting of process equipment and clean utility systems.

Skills

CQV/Startup experience
Experience supporting critical utilities
Strong GMP documentation skills
Excellent communication skills

Education

Bachelor’s degree in Engineering or related technical discipline

Tools

DeltaV
Rockwell
Kneat
ValGenesis

Job description

Intellectt Inc is looking for experienced CQV Engineers for a large-scale greenfield biopharmaceutical manufacturing project located in North Carolina. The role involves executing commissioning, qualification, and startup activities for GMP manufacturing equipment and supporting critical utilities like WFI and HVAC. Ideal candidates should have over 5 years in CQV/Startup within the pharmaceutical industry and possess strong documentation skills. The environment is dynamic, and engineers are expected to drive project timelines effectively.
Get your free, confidential resume review.
or drag and drop your file here.
Similar jobs

Similar jobs worth comparing

CQV Engineer
CQV Engineer

Intellectt Inc • Irvine (CA)

On-site
USD 90,000 - 120,000
CQV Engineer: Biopharma Commissioning & Qualification
CQV Engineer: Biopharma Commissioning & Qualification

Project Delivery Partners Pte Ltd • Raleigh (NC)

On-site
USD 75,000 - 95,000
CQV Engineer: GMP Biopharma Equipment & Utilities
CQV Engineer: GMP Biopharma Equipment & Utilities

Stark Pharma • Philadelphia

On-site
USD 90,000 - 130,000
Contract CQV Engineer: Biopharma Commissioning & Validation
Contract CQV Engineer: Biopharma Commissioning & Validation

Intellectt INC • North Carolina

On-site
USD 114,616,000 - 157,597,000
CQV Engineer
CQV Engineer

Stark Pharma • Philadelphia

On-site
USD 90,000 - 130,000
Senior CQV Engineer for GMP Bioprocess Systems
Senior CQV Engineer for GMP Bioprocess Systems

GxP Associates • North Carolina

On-site
USD 110,000 - 160,000
On-Site Senior CQV Engineer — GMP Validation Lead
On-Site Senior CQV Engineer — GMP Validation Lead

Visium Resources, Inc. • Raleigh (NC)

On-site
USD 110,000 - 150,000
CQV Engineer: Risk-Based Pharma Commissioning Lead
CQV Engineer: Risk-Based Pharma Commissioning Lead

Shoolin Inc • California (MO)

On-site
USD 90,000 - 120,000
CQV Engineer – Pharma Commissioning & Qualification
CQV Engineer – Pharma Commissioning & Qualification

Project Delivery Partners Pte Ltd • San Diego (CA)

On-site
USD 80,000 - 100,000
Onsite Validation Engineer - Pharma & Biotech CQV Expert
Onsite Validation Engineer - Pharma & Biotech CQV Expert

KKR Consulting • North Carolina

On-site
USD 75,000 - 95,000