LSC have an exciting opportunity for CQV Engineer to support projects in a cutting-edge pharmaceutical company based in Co. Wicklow.
As a CQV Engineer in the project group, you'll play a crucial role in shaping the future of pharmaceutical manufacturing.
ABOUT THE ROLE?
- Lead commissioning and qualification activities for state-of-the-art process and packaging equipment, facilities, utilities, and computerized systems
- Develop, review, and approve cGMP documentation for equipment, facility, utility, and computerized systems validation
- Drive project success from design through commissioning and qualification phases
- Manage vendor relationships and ensure compliance with quality standards
- Spearhead change control initiatives and foster a culture of continuous improvement
ARE YOUR SKILLS A MATCH?
- Bachelor's degree in Engineering, Science, or a related technical field (engineering degree preferred)
- Minimum 5 years of experience in pharmaceutical manufacturing, validation, operations, or engineering
- Proven validation expertise in Process and Packaging Equipment (OSD), Facilities and Utilities, and Computerized Systems.
- Strong technical writing skills and experience with GMP documentation
- Proficiency in risk assessment and risk-based approach to validation activities
- Experience with Electronic Documentation Management Systems (KNEAT, VEEVA, TRACKWISE)
- Excellent problem-solving abilities and innovative thinking
Apply directly through this advert or contact Kathy Gillen on 021 4718212 to get more details on this great opportunity.
Applicants must have a 12 month valid work visa for Ireland. LSC do not offer visa or work permit sponsorship.
