Are you a skilled CQV Engineer with experience in the biotechnology/pharmaceutical industry? Do you enjoy working in a dynamic team environment where you can make a difference and drive the completion of tasks? We are seeking a highly motivated individual to join our Biopharmaceutical Client located in Sligo. This role is a permanent full-time position.
What You'll Receive
22 Days Holidays
Responsibilities | Detailed Job Description Available on Request
As a CQV Engineer, you will be responsible for:
Planning, generating, executing, and reporting Commissioning, Qualification, and Validation (CQV) activities for the facility, utilities, and process equipment.
Supporting both new and legacy equipment.
Approving contractor designs and documentation.
Conducting field verifications during tests.
Participating in startup activities.
Managing vendor and contractor attendance.
Supporting reviews and investigations.
Ensuring technical accuracy and adherence to cGMP.
As a CQV, your duties will involve:
A minimum of an Honours degree in an Engineering or Science discipline.
At least 5 years experience in the biotechnology and/or pharmaceutical industry in a CQV role.
Proven experience in authoring, reviewing, and executing CQV reports & activities on a variety of Facility, Utility, and Process Equipment is essential.
If this CQV Engineer role interests you, please contact Emma Cawley today.
Click here to book an online appointment to discuss this role: