LSC have a great contract opportunity for a QA Documentation II to join a Multinational Pharmaceutical Company based in Dublin.
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).
o Generation, development and communication of project metrics and status updates.
ABOUT YOU – 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 Knowledge of cGMP requirements for documentation control.
o Direct experience with firstDoc eDMS or similar Documentum-based platform.
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 Siobhan Cummins at LSC on 021-4777329 if you have anymore questions about this QA Documentation II opportunity!