The QC Manager will be responsible for managing the Chemical Analytical Sciences team and owning, facilitating, and undertaking activities pertaining to CAS within QC. Based in the Dublin site of a renowned biopharmaceutical multinational, the successful candidate will focus on compliance, continuous improvement and implementing a lean culture and Right First Time (RFT) for CAS duties and testing, including release of commercial and global release testing. The role also represents the QC unit by liaising with internal and external stake holders
-Bachelor’s degree in a Science related field is required.
-6+ years of biopharmaceutical QC experience or related quality control or GMP laboratory experience in the pharmaceutical or medical device industry, with of 2 – 3 years of specific sample management/ stability programme management experience is desirable.
-Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products.
-Possess key competencies to include planning/organisation, problem solving, communication, teamwork, flexibility, coaching and motivating.
-Proven experience of leading teams.
For more information and a full job spec contact Nicola on (phone number removed) or email your CV in the strictest confidence to
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