CQV/Validation Engineer

CAI

The Municipal District of Carlow

On-site

EUR 45,000 - 72,000

Full time

14 days+
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Job summary

CAI is seeking a CQV Engineer in Ireland to conduct and lead commissioning, qualification, and validation activities in life sciences. The role requires strong communication and problem-solving skills, a science or engineering degree, and at least three years of relevant experience. Join a team committed to delivering high standards and ensuring safety in the pharmaceutical manufacturing industry.

Qualifications

  • 3+ years in CQV SME roles for life sciences.
  • Proficient in life science manufacturing processes.
  • Able to travel domestically and internationally.

Responsibilities

  • Conduct and lead Commissioning, Qualification, Validation activities.
  • Manage C&Q documentation and execution lifecycle.
  • Deliver C&Q activities to meet project schedules.

Skills

Excellent communication
Problem-solving
Customer service focus

Education

BS or MS in relevant science or engineering field

Job description

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.

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 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 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, FAT's, 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.

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.

Seniority level
  • Seniority level
    Mid-Senior level
Employment type
  • Employment type
    Full-time
Job function
  • Job function
    Quality Assurance
  • Industries
    Pharmaceutical Manufacturing

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