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.
Are you Ready
Our approach is simple; we put the clients 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 persons success is everyones 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 a CQV Engineer to join our growing operations in Ireland The role of a CQV Engineer in CAI is to:
Conduct and lead Commissioning Qualification Validation team activities with a direct regard for Safety.
Managing the C&Q documentation and execution lifecycle from SLIA generation through to OQ completion.
Generating C&Q Procedures for projects.
Approval of TOPs.
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.
Preparation of Qualification Summary Reports (QSR) and management of Requirement Traceability Matrix (RTM)
Execution of Design reviews shakedown commissioning FATs IQ OQ PQ activities.
Management of any aspect of C & Q verification as requested i.e. Change Controls Management of Contractors and Vendors document control punch list management.
Coordinate with project contractors and equipment vendors to execute required tests.
Allocate project resources for efficient execution of project deliverables.
Coordinate support during C&Q execution -
Position Requirements:
BS or MS in a relevant science or engineering field or equivalent
3 years in CQV SME roles for life sciences Clean Utilities/Filling experience preferable
Excellent oral and written communication skills
Excellent problem-solving skills
Customer-service focused.
Proficient in life science manufacturing processes in areas such as biotech aseptic fill/finish OSD Gene Therapy or equivalent experience.
Able to travel domestically and internationally if required.