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 if you have any more questions about this opportunity!
Skills: Quality Assurance Pharmaceuticals Document Control Specialist Quality Systems