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About AbbVie

AbbVie’s mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women’s health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn.

QC Lab Analyst

Sligo, Connaught, Ireland Req ID 2209038 Category Quality Assurance Division AbbVie


Want to make a global impact? We offer that

Want to be part of a Great Place to Work in Ireland? We offer that too

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 currently recruiting a QC Lab Analyst for our high-performing team in Manorhamilton Rd, Sligo. 

Are you intrigued? Do you want to learn more?

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

  • Maintain and comply with Laboratory Documentation and Computerized Systems Data Integrity requirements.
  • Understand Regulations and business processes required to maintain Laboratory Data Integrity.
  • Be responsible for housekeeping duties in the lab.
  • Be responsible for the timely completion of chemical testing of raw material.
  • Ensure that all test equipment is used and maintained correctly.
  • Be responsible for raising change requests and data verification as assigned.
  • Ensure all in-process sampling and testing are completed in a timely manner.
  • Maintain up-to-date, complete, and precise records of all tests performed.
  • Adhere to cGMP and GLP requirements.
  • Assist in the resolution of quality problems as required.
  • Develop and change in-house laboratory procedures as appropriate.
  • Aid in training of new analyst.
  • Support the transfer of new products.
  • Adhere to and support all EHS & E standards, procedures and policies.

Education and Experience:

  • 3rd level qualification in a relevant Science discipline required.
  • A minimum of 6 months of experience in HPLC or GC.
  • Experience operating to cGMP standards utilizing laboratory equipment. 
  • Previous experience in a pharmaceutical manufacturing environment is desirable but not essential.

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. 

Travel: No
Job Type: Experienced
Schedule: Full-time
ABBVIE

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Equal Employment Opportunity | Reasonable Accommodation