LSC have a great contract opportunity for a QA Document Control Specialist to join a Cork based Biopharmaceutical company.
If you have 2+ years of experience within a GMP environment and are ready for your next challenge, this could be the perfect project for you!
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
- Process site-controlled documents on the site Document Control System.
- Approve document change controls and establish document effective dates.
- Complete work according to established priorities and policies to assure product documentation is delivered on schedule.
- Support and train other staff members on the implementation of global improvements related to the Document Control System.
- Train and support other staff members on the use of the Document Control System.
- Maintain the Sites Document Store and escalate any potential issues.
- Control and issue controlled document numbers as required.
- Support Inspection Readiness for the site and the site in preparation for upcoming inspections.
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- Strong communication and organisational skills required.
- Experience with QMS and EDMS systems is desirable.
- Experience with excel / metrics generation is desirable.
Applicants interested in our contracting opportunities within the pharmaceutical sector in Ireland are required to have a Stamp 1G or a Stamp 4 visa. Please understand that we are unable to provide visa sponsorship. Thank you for your understanding.
Apply via this advert or contact Siobhan Cummins at LSC on 021-4777329 if you have any more questions about this opportunity!
