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Quality Control Analyst

AbbVie

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AbbVie

Quality Control Analyst

Onsite Sligo, Ireland Full Time Junior
Posted 5 days ago
Save Job
powertofly approved What AbbVie Has to Offer:

Our work can—and does—have a tangible, lasting impact on millions of people. But it’s not just the results that matter. How we achieve them matters, too. Leading with purpose, we work to build a more sustainable future for generations to come. We do that by putting our expertise, resources and talent to work to make a real difference for patients, communities and our world.

Job Details


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, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.


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. This is also a rotating shift position.

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 an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled. 

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

Required Skills
  • HPLC
  • GC
  • cGMP
  • laboratory equipment
  • pharmaceutical manufacturing
Company Details
AbbVie
 Chicago, IL, United States
Work at AbbVie

Together, we break through We believe the paths we take to achieving our breakthroughs matter. At AbbVie, every one of our 50,000 employees is a... Read more

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