QC Analyst - Cork, Ireland - 12 Month Contract
Are you interested in joining a world leading biopharmaceutical company, focused on developing advanced and innovative treatments for those suffering with rare diseases?
This is a fantastic opportunity to work in a state-of-the-art facility in Cork.
You will be joining a leading biopharmaceutical company who focus on a range of products which are life-changing for individuals.
Responsibilities
Perform primary review of QC raw data and trend results
Prepare protocols, summaries, and reports, including documents submitted directly to pharmaceutical regulatory agencies
Draft and update QC Standard Operating Procedures (SOPs)
Act as a technical subject matter expert (SME) and provide training and support to other analysts in areas of expertise
Evaluate analytical and microbiological results against defined acceptance criteria
Qualifications
BSc in a scientific or engineering discipline with extensive relevant cGMP laboratory experience
MSc with relevant cGMP laboratory experience
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