CQV Engineer

Job Description

Are you a CQV Engineer with a desire to learn and develop within the Pharmaceutical industry, I have an excellent opportunity in Cork for the right person.

CQV Engineer:

We are seeking highly motivated and talented individuals to join an incredible team of skilled problem solvers. Qualified candidates must have a desire to learn, apply, engage, within the Pharmaceutical field.

Daily Responsibilities:

• Draft and execute Commissioning and Qualification (C&Q) documentation and services for client facility, utility, process, and equipment.
• Performs/executes the validation/verification studies (FAT, SAT, CTP, IQ, OQ, PQ) for cleaning, sterilization, equipment, systems, utilities, and processes for qualification and/or requalification.
• Prepare written validation reports with high level of detail and organization.
• Develop and complete deliverables related to CQV activities as needed to ensure objectives are met.

Qualification and Requirements:

• Bachelor's or Master's degree in Bioengineering, Biomedical Engineering, Mechanical Engineering, Chemical Engineering, or Science related technical degree preferred.
• 3-5 years' experience of validation and/or quality in a regulated, manufacturing environment within the biotechnology, pharmaceutical or medical device industry.
• Experience with Quality Systems (handling Change Controls, Non-Conformances, Deviations, CAPAs)

Morgan McKinley is acting as an Employment Agency and references to pay rates are indicative.

BY APPLYING FOR THIS ROLE YOU ARE AGREEING TO OUR TERMS OF SERVICE WHICH TOGETHER WITH OUR PRIVACY STATEMENT GOVERN YOUR USE OF MORGAN MCKINLEY SERVICES.