Pharma Validation Engineer (Contract) - CSV & 21 CFR Expert

Inteletech Global Inc; Jersey City (NJ); On-site; USD 55,104; Full time

Job summary

A leading global consulting firm is seeking a Validation Engineer in Summit, New Jersey. This contract role requires 4-7 years of experience in the pharmaceutical or biotech sectors with a strong background in Computer System Validation (CSV). Responsibilities include maintaining validated systems, drafting validation documents, and supporting cross-functional teams. Ideal candidates must have a Bachelor's degree in Engineering or Computer Science, and excellent technical writing skills are a must. Competitive compensation at $40.00 per hour is offered.

Qualifications

• 4-7 years of experience in the pharmaceutical or biotech industry.
• Strong understanding of 21 CFR Part 11 and data integrity.
• Experience in interpreting engineering documentation and technical drawings.

Responsibilities

• Maintain qualified/validated equipment and systems.
• Draft and execute validation documents like Validation Plans and Summary Reports.
• Support change management and document lifecycle activities.

Skills

Computer System Validation (CSV)

Technical writing

Presentation and communication skills

Attention to detail

Education

Bachelor’s degree in Engineering or Computer Science

Job description

A leading global consulting firm is seeking a Validation Engineer in Summit, New Jersey. This contract role requires 4-7 years of experience in the pharmaceutical or biotech sectors with a strong background in Computer System Validation (CSV). Responsibilities include maintaining validated systems, drafting validation documents, and supporting cross-functional teams. Ideal candidates must have a Bachelor's degree in Engineering or Computer Science, and excellent technical writing skills are a must. Competitive compensation at $40.00 per hour is offered.