Senior Validation Engineer - GMP CQV Specialist

CAI; Harrisburg (Dauphin County); On-site; USD 70,000 - 95,000; Full time

Job summary

A professional services company in Harrisburg is seeking a qualified individual with a Bachelor's degree in Engineering, Chemistry, or Life Sciences and 3+ years’ experience in the Pharmaceutical industry. The role involves performing CQV activities, supporting documentation, and coordinating project logistics. Candidates should have a customer-focused mindset, strong problem-solving skills, and be willing to travel. This is a dynamic opportunity to contribute to critical solutions in high-stakes environments.

Qualifications

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

Responsibilities

• Perform CQV activities with a focus on safety.
• Generate and review qualification-related documents.
• Coordinate support during CQV execution.

Skills

Problem-solving

Communication

Customer-focused

Education

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

Job description

A professional services company in Harrisburg is seeking a qualified individual with a Bachelor's degree in Engineering, Chemistry, or Life Sciences and 3+ years’ experience in the Pharmaceutical industry. The role involves performing CQV activities, supporting documentation, and coordinating project logistics. Candidates should have a customer-focused mindset, strong problem-solving skills, and be willing to travel. This is a dynamic opportunity to contribute to critical solutions in high-stakes environments.