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Located near Westport, our global pharmaceutical client is seeking a Validation Engineer to join their state‑of‑the‑art manufacturing facility. The company focuses on investing in research and development to drive scientific innovation and deliver life‑changing medicines. With thousands of employees worldwide and continued growth across their network, this is an excellent opportunity to join a leading organisation shaping the future of healthcare.
What You’ll Do
Over-see, coordinate, guide and implement the site validation master plan under prospective, concurrent, and retrospective validation studies in a timely manner, with the relevant engineers.
To actively work on validation projects, being the departmental point person and completing all associated project documentation in line with current corporate and regulatory expectations.
Participate in risk assessment process for all business units & participate in design review process for all business units.
Tracking and generation of weekly metrics (GTW QMS, EHS, Compliance Wire etc.)
What you’ll need
Bachelor’s degree required in science based or engineering discipline.
Experience in Pharmaceutical company.
Excellent project management skills.
Proficient in use of Microsoft Office suite of programs.
Critical thinking and problem-solving skills. xcfaprz
Apply now to become a part of this life changing project!
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Sprachkenntnisse
- English
Hinweis für Nutzer
Dieses Stellenangebot wurde von einem unserer Partner veröffentlicht. Sie können das Originalangebot einsehen hier.