A fantatstic opportunity for a QC Micro Analyst with 2 years' pharmaceutical industry experience to join the team at a leading bio-pharma company in Cork on a 2 cycle or 4 cycle shift pattern for 12 months.
Technical knowledge of analytical techniques and knowledge of related laboratory equipment in the area of microbiological, chemistry and biochemistry testing of Bulk API and final drug product is desired for this role Duties include: Performing a wide variety of microbiology, chemistry or biochemistry testing to support utilities, raw material, in process, bulk and drug product release.
Initiates and completes, CAPAs and Change Controls in accordance with site procedure Writes new and updates current procedures on electronic documentation system.
Bioburden Endotoxin Sterility Testing Microbial Identification using genetic methods Experience with electronic systems such as LIMS, Electronic Lab notebooks, Empower, Trackwise desired.
A minimum of 2 years experience within the Pharmaceutical Industry Knowledgeable of FDA/EMEA regulatory requirements applicable to pharmaceuticals and aseptic products.
BY APPLYING FOR THIS ROLE YOU ARE AGREEING TO OUR TERMS OF SERVICE WHICH TOGETHER WITH OUR PRIVACY STATEMENT GOVERN YOUR USE OF MORGAN MCKINLEY SERVICES.