Senior CQV Validation Engineer — Pharma, GMP, ESOP

CAI; Indianapolis (IN); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Comprehensive Health Insurance coverage

24 days of Paid Time Off

ESOP/401K - 15% Company Contribution

Company paid Life Insurance

Company paid Long Term Disability

Job summary

A leading company in life sciences is seeking a professional for CQV Execution and Safety. Responsibilities include performing commissioning, qualification, and validation activities, ensuring compliance with documentation, and managing project planning. The ideal candidate will have a Bachelor's degree in Engineering or Life Sciences, alongside 3+ years of experience in a GMP environment. The position offers comprehensive health insurance, paid time off, and a 401K plan.

Qualifications

• 3+ years of related experience in the Pharmaceutical/Life Sciences industry.
• Essential experience in a GMP (Good Manufacturing Practice) environment.
• Willingness and flexibility to travel throughout the U.S. and potentially internationally.

Responsibilities

• Perform CQV activities with a strong focus on safety.
• Support the generation and review of C&Q procedures.
• Coordinate support and logistics during CQV execution.
• Support execution of design reviews, commissioning activities.

Skills

Outstanding oral and written communication skills

Strong problem-solving abilities

Customer-focused mindset

Ability to work in GMP environments

Education

Bachelor's degree in Engineering, Chemistry, or Life Sciences

Job description

A leading company in life sciences is seeking a professional for CQV Execution and Safety. Responsibilities include performing commissioning, qualification, and validation activities, ensuring compliance with documentation, and managing project planning. The ideal candidate will have a Bachelor's degree in Engineering or Life Sciences, alongside 3+ years of experience in a GMP environment. The position offers comprehensive health insurance, paid time off, and a 401K plan.