CQV Engineer

Netherlands  /  Europe/Ireland  /  Full Time

About CAI:
CAI is a 100% employee-owned company established in 1996, that has grown year over year to nearly 700 people worldwide. We provide commissioning, qualification, validation, start-up, project management and consulting services related to operational readiness to FDA regulated and other mission critical industries.
Meeting a Higher Standard:
Our approach is simple; we put the client’s interests first, we do not stop until it is right, and we will do whatever it takes to get there.
As owners of CAI, we are committed to living our Foundational Principles, both professionally and personally:
·       We act with integrity
·       We serve each other
·       We serve society
·       We work for our future
With employee ownership, one person’s success is everyone’s success; we work diligently to accomplish team goals. We place Team Before Self, demonstrate Respect for Others, and possess a can-do attitude. That is how we have grown exponentially.
CAI agents will be exposed to cutting edge technologies in the advanced medicine space. You will have an opportunity to work with recognized subject matter experts allowing YOU to be a key player in bringing lifesaving therapies to market. As part of our company culture, we invest in YOUR future, and commit to hands on certifications as well as professional training. Our collaborative culture ensures that our customers benefit from exemplary work across our entire range of professional services.
Requirements include:
We are now seeking CQV Engineers to join our operations in the Netherlands for the Gene & Cell Therapy industry The role of a CQV Engineer in CAI is to:
·       Perform Commissioning, Qualification, Validation team activities with a direct regard for Safety.
·       Generation & Review of System User Requirements, Design Qualifications & IOQ Protocols.
·       Execution of IOQ Protocols for Facility, Utility & Lab Equipment.
·       Facilitate scoping / planning of commissioning spares and consumables.
·       Deliver the C&Q activities as required to meet the schedule
·       Track progress of C&Q activities as required.
·       Coordinate with equipment vendors to execute required tests.
·       Coordinate support during C&Q execution
Position Requirements:
·       BS or MS in a relevant science or engineering field, or equivalent
·       5+ years’ experience in a CQV role for life sciences and/or Gene Cell Therapy
·       Experience with Clean Utilities, Cleanrooms, QC/lab equipment or COTS validation is advantageous.
·       DI/CSV/security experience is required.
·       Excellent oral and written communication skills.
·       Excellent problem-solving skills.
·       Customer-service focused.
·       Proficient in life science manufacturing processes in areas such as Bio-Pharma, , Gene Therapy or equivalent experience.
·       Able to travel domestically and internationally if required. 
We are an equal opportunity employer; we are proud to employ veterans and promote a diverse culture in our workplace. Diversity is a strength for our global company. We pledge that CAI will be operated in a way that is fair and equitable to all – our employees, our customers, and the broader society. This job description is not all inclusive and you may be asked to do other duties. 



(Varies by Country, Below is a General Overview)

  • 100% Employee Owned
  • 24 Days PTO/5 Sick days per year + Additional Holidays depending on Country
  • Medical / Dental / Vision (In accordance with each countries’ applicable regulations)
  • Professional Development (Approximately $5,000 paid career-related, continuing education)
  • ESOP/401k – 15% Company Contribution
  • Company Paid Long-Term Disability
  • Company Paid Life Insurance
  • Company Paid Parental Leave (In accordance with each countries’ applicable regulations)
  • Other Benefits Depending on Country