LSC has a fantastic opportunity for a Validation Engineer- Documentation to join an advanced global team in Denmark that promotes self-development, encourages collaboration, and fosters a learning environment. This is a chance for you to be a part of a fast-growing, multicultural company that has a compelling vision for shaping the future of medicine.
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
- Primarily support on validation Documentation: Write and review Qualification document and reports.
- Data evaluation, review and reporting including deviation handling.
- To some extend also be part of execute PQ testing
- Some flexibility in terms of working hours is required.
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- 5-7 years' experience in performing and document qualifications.
- 5-7 years of relevant industry experience from biological drug substance manufacturing.
- Experience with PQ execution and documentation of the testing.
- Familiar with risk Based Qualification, Kneat, DeltaV and working temperature data loggers.
- Hold a bachelor's degree or higher in a relevant discipline.
Note: Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold an EU/UK Passport to apply! Apply via this advert or contact Siobhan Cummins at +353 214777329 if you have any more questions about this opportunity!
