LSC have a great contract opportunity for a Document Controller to join a Limerick based Biotech Drug Substance Manufacturing Facility.
This is an exciting opportunity to work with next-gen manufacturing technologies, advanced data collection and analysis platforms that will result in safety and quality improvements, increased productivity, and variability reduction.
If you have at least 3 years of relevant experience in a cGMP environment and ready for your next challenge, this could be the perfect project for you!
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
- Ensure compliance to Global and Local Documentation and Records Management requirements.?
- Establish new and modify existing documentation in a manner which will achieve accuracy and avoid errors and product recalls or issues.
- Manage the flow of documents from initiation of workflow to approval.
- Day to day management and monitoring of assigned workflows.
- Review and accept incoming documents are complete and aligned with GDP, support initial review of documentation for end-users.
- Ensure that technical documentation is kept up to date with the support of technical team members for the creation of content.
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- Ability to create prototype implementations to test documentation accuracy and effectiveness
- Experience working in Document control in a GMP environment.
- A relevant third level business / science qualification with at least 3 year's work experience ideally from a regulated industry.
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!
Apply via this advert or contact Gráinne Hodnett at LSC on 021-4777329, if you have any more questions about this opportunity!
