Together, we create the capabilities of tomorrow.
You’re here to make a difference. We have the science to turn you into difference makers.

Welcome to AbbVie!
We are a global, research-based biopharmaceutical company that combines the focus and passion of leading-edge biotech with the expertise and capability of an established pharmaceutical leader. Redefining what is possible is our business and our passion. Our goal is to help patients live healthier lives and we are proud to be a Great Place to Work.

We are recruiting a Senior QC Micro Analyst to join our team in Ballytivnan, Sligo.

A snapshot of your key responsibilities as a Senior QC Micro Analyst would be:

• Understand all Regulations and business processes required to maintain Laboratory Data Integrity and compliance.
• Lead the environmental and microbiological tests programs and work along with the QC analysts to implement continuous improvements.
• Carry out a variety of routine testing including but not limited to Bioburden, Endotoxin, Growth Promotion, TOC, pH, Conductivity, Nitrates, density and protein concentration.
• Lead the Micro QC analysts during any batch or APS runs.
• Define and update procedures for plant relative to microbiological and environmental testing.
• Support validation of equipment.
• Lead test method transfer of microbiological methods into the lab.
• Develop microbiological laboratory procedures and overall workings within the lab environment.
• Maintain up-to-date and detailed records of all tests performed. Review and approve testing data and be competent in the use of LIMs system.
• Adheres to and supports all EHS & E standards, procedures and policies.
• Lead and support any internal/external audits.
• Lead investigations into Out of Specification (OOS) results, LIRs and NCRs for the lab.
• Act as a delegate in the absence of the Microbiology Lab Lead.
• Other duties as assigned.

Education and Experience:

• Third level qualification in microbiology required or equivalent science discipline.
• A good knowledge of aseptic processes' manipulation together with experience within a GLP/GMP environment and knowledge of current EU/FDA/ICH/HPRA guidelines.
• Experience is industry is desirable.

So, are you ready to join our team?
It’s important to remember, AbbVie is an Equal Employment Opportunity Employer; we value bringing together individuals from diverse backgrounds to develop innovative solutions for patients and being part of an inclusive work environment.

AbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community, and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.