Validation Quality Engineer

LocationPortlaoise, Ireland
Reports ToQuality Assurance Manager

Greenfield is looking for a Validation Quality Engineer to join our growing team.

Who We Are:

Greenfield Global is a leading producer and supplier of high-value, mission-critical raw materials, ingredients, and additives that are vital to businesses and integral to a lower carbon economy. From start-ups to the largest brands in the world, customers trust Greenfield’s extensive portfolio of premium products, regulatory expertise, and industry-leading service to improve people’s lives and the health of the planet.

Why Join Greenfield?

We innovate, collaborate, and work with purpose. By unlocking the potential of people, partnerships, and nature to accelerate sustainable solutions for the health of the planet, our work has a positive impact on the environment around the world. We’re always looking for people who can bring new talents and experience to our team.

Your Experience Should Include:
  • Must have a third level qualification, at a minimum to degree level, in Engineering, Quality, or Science
  • 3 -5 years’ experience in a similar role in the Pharmaceutical and/or Medical Device Industry
  • In-dept knowledge of validation principles
  • Previous experience in a GMP regulated environment essential.
Job Responsibilities:
  • Develop validation documentation e.g. Protocol and reports for IQ’s, OQ’s, PQ’s
  • Manage the validation master list
  • Determine Critical Quality Control Points with the Quality Department
  • Complete Periodic Reviews
  • Manage the archiving and filing of validation documentation
  • Implement Data Integrity practices and policies.
  • Manage Software validation program
  • Drive solutions, in conjunction with the appropriate department, to ensure customer related validation problems are communicated and corrective actions are in place and closed in a timely manner
  • Lead data/presentations and attend review meetings with the customer
  • Implement best practices principles into Greenfield QMS as applicable
  • Support internal and supplier audits
  • Trending and tracking of Validation data to drive improvements.

Total Compensation & Care:

  • Base salary dependent on experience and demonstrated performance
  • Formal and informal training opportunities
  • Comprehensive health and dental benefits
  • Income protection: short- and long-term disability coverage, life insurance, paid
    personal sick time
  • Vacation time exceeding industry standards
  • Company funded retirement savings program with individual contribution
  • Meaningful and challenging work
  • Curated intentional culture focused on growth and development, engagement, and

About Us

We own and operate five distilleries, four specialty chemical manufacturing and packaging plants, and three next-generation biofuel and renewable energy R&D centers. This integrated model enhances supply chain transparency, quality control, custom formulation development, and ultimately customer satisfaction.

Core Values

  • Honesty
  • Integrity
  • Respect
  • Commitment
  • Openness to Change
  • Core Principles


We are constantly seizing opportunities to develop new products, processes and methods to meet the diverse and demanding requirements of our customers.


We are part catalyst, part collaborator. We work with partners to get the most out of our existing products, and to develop custom solutions for our customer requirements.


Our commitment to give back to local communities in the US and Canada goes beyond the bottom line. We give back to the planet by processing renewable resources into low carbon fuels and chemicals.


Our team is not only fast, we has the flexibility and creativity to pivot with customer needs to develop custom-made, on-time solutions.


At every plant, and for every customer, for every shipment, we put quality first. We operate a tight, transparent supply chain while meeting the highest regulatory standards.