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AbbVie QC Lab Analyst in Sligo, Ireland

Company Description

AbbVie's mission is to discover and deliver innovative medicines and solutions 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, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X (https://twitter.com/abbvieireland) , Facebook, Instagram (https://www.instagram.com/abbvieireland/) , YouTube and LinkedIn.

Pharmaceutical Research & Development

AbbVie pharmaceuticals combines advanced science with expertise to make strides in drug and treatment discovery, making a remarkable impact on people's lives

Job Description

We are currently recruiting a QC Analyst for our high-performing team in Manorhamilton Rd, Sligo. This is a 12 month fixed-term contract.

A snapshot of your key responsibilities as a QC 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.

Qualifications

  • 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.

Additional Information

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.

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