Senior CQV Validation Engineer – Life Sciences

CAI; Philadelphia (Philadelphia County); On-site; USD 70,000 - 90,000; Full time

Job summary

A professional services company based in Philadelphia seeks individuals for a role focusing on Commissioning, Qualification, and Validation (CQV) activities in the pharmaceutical sector. Candidates should possess a Bachelor's degree in relevant fields and have a minimum of three years' experience in GMP environments. Responsibilities include ensuring safety during operations, reviewing procedures, and coordinating project resources. Candidates should expect travel within the U.S. and internationally. Competitive compensation provided.

Qualifications

• Relevant experience can substitute for education.
• Essential experience in a GMP (Good Manufacturing Practice) environment.
• Willingness and flexibility to travel throughout the U.S. and potentially internationally.

Responsibilities

• Perform Commissioning, Qualification, and Validation (CQV) activities focusing on safety.
• Support the generation and review of C&Q procedures for client projects.
• Coordinate support and logistics during CQV execution.

Skills

Outstanding oral and written communication skills

Strong problem‑solving abilities

Customer‑focused mindset

Education

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

3+ years of related experience in the Pharmaceutical/Life Sciences industry

Job description

A professional services company based in Philadelphia seeks individuals for a role focusing on Commissioning, Qualification, and Validation (CQV) activities in the pharmaceutical sector. Candidates should possess a Bachelor's degree in relevant fields and have a minimum of three years' experience in GMP environments. Responsibilities include ensuring safety during operations, reviewing procedures, and coordinating project resources. Candidates should expect travel within the U.S. and internationally. Competitive compensation provided.