LSC have an exciting contract opportunity for a QA Documentation Specialist to join a biopharmaceutical company in Dublin focused on serving patients with severe and ultra-rare disorders through the innovation, development and commercialization of life-transforming therapeutic products.
If you have 3-5 years’ experience within the pharma industry or related field and are ready for your next challenge, this could be the perfect project for you!
ABOUT THE PROJECT – KEY RESPONSIBILITIES:
o Assessment, coordination and withdrawal of documents within the Electronic Document Management System (eDMS).
o Collaboration with document owners to facilitate efficient processing of impacted documentation.
o Generation of queries and reports from eDMS.
o Interface between Document Control and Training Operations to ensure updated documents are transitioned into the Learning Management System (LMS).
ABOUT YOU SKILLS – ARE YOUR SKILLS A MATCH?
o B.Sc. in science/engineering with a minimum of 3-5 years’ experience in cGMP Quality environment; or equivalent combination of education and experience
o 3-5 years’ experience within the pharma industry or related field.
Note: Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold a Stamp 1G/Stamp 4 visa to apply!
To apply submit your CV via this advert or contact Regina Carroll at LSC on 021-4777329 if you have any more questions about this QA Documentation opportunity!