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Analyst, Quality
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AbbVie

Analyst, Quality

Onsite Sligo, Ireland Full Time
Posted 2 hours 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

In AbbVie Ballytivnan, we are recruiting for a Quality Analyst to join our team. The purpose of his role is to provide an effective testing and analytical service to the plant ensuring that products manufactured are tested to specification on time and plant quality and safety goals are met.

This role will report directly to the QC Supervisor.

What you will do:

  • 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 tests, including HPLC, protein concentration (SoloVPE), pH, conductivity, and TOC.
  • Be responsible for raising change requests and data verification as assigned.
  • Ensure all in process sampling and testing is 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.
  • Developing and changing of in-house laboratory procedures as appropriate.
  • Aid in training of new analyst.
  • Supports the transfer of new products.
  • Adheres to and supports all EHS & E standards, procedures and policies

Qualifications

What you will need:

  • A third level qualification in a science or quality discipline
  • Minimum 2 years’ Experience in a similar role in a Pharmaceutical or Sterile Manufacturing environment
  • Excellent written and verbal communication skills with a strong attention to detail.

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

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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