A QC analyst required for a permanent postion with a Pharmaceutical company based in Cork. The site is an FDA approved API manufacturing facility that offers both drug substance and particle engineering on a [...] more details
Are you looking for an opportunity to advance your automation experience in a leading edge medical device facility with a focus on process innovation, automation and continuous improvement? We have an excellent [...] more details
Have you spent over 3 years in a pharma/biopharma auditing role? This role has responsibility for the planning and execution of audits to assess ongoing compliance with government regulations and corporate standards [...] more details
A Validation Specialist is required for this Cork based Biopharmaceutical company that manufactures low volume bulk API for Phase III clinical trials, initial product launch and long term market support. The team on [...] more details
Are you an Import/Export Specialist ? Our client requires a self-starter to monitor Customs Community Directives and biopharmaceutical regulations, aligning business process to comply with changing requirements. [...] more details
BioProcess
Commissioning Validation
E/I Engineers
EHS
Engineering
IT & Automation
Medical Device
QC Laboratory
Quality Assurance
Supply Chain Procurement
