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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.

Job Description

You’re driven by the science. By discovery. By the unknown. Take on the work that challenges you, so you can challenge the status quo. At AbbVie

Welcome to AbbVie!

At our Westport site in Co. Mayo, we are now hiring an Analytical Technology Specialist to join our talented and ambitious team, on a 1 year fixed term contract.

As our new Analytical Technology Specialist, you will support the operations of the Bioassay Laboratory conducting Cell-Based Potency Assay (CBPA) testing of product release, stability and investigation lots.

With an exciting pipeline of products and a great salary and benefits package, this may be the ideal opportunity to develop your career with an industry leader.

So if you are interested in joining AbbVie Westport, read below to find out more…

In your new role, you will:

• Complete writeups on time and participate in the review of team analytical work. Conduct validation testing for key projects in the Bioassay group.

• Generate validation documentation, update SOPs, oversee the progression of key validation projects within the Bioassay group, JMP analysis, generate toxin trends, qualification of critical reagents and perform lab duty tasks as required.

• CBPA analysis of release, stability and investigational analytical activities.

• Support and execute Method Transfer and Validation activities associated with key biological drug product projects.

• Compiling and review of Laboratory documentation (e.g. SOPs, methods, validation documentation etc.).

• Support regulatory inspections as required.

• Perform lab duty tasks to maintain a high standard of housekeeping within the laboratory.

• Drive Root Cause Analysis investigations.

• Support and lead Laboratory projects to ensure timelines are met successfully.

• Manage group activities as required and lead projects to ensure completion.

• Participate at meetings and provide input to key projects and improvements within the group.

• Adhere to and support all EHS procedures and policies.

Qualifications

So does this role sound exciting? then read on.....

To succeed in this role, you will have the following Education and Experience:

• You will have a 3rd level qualification in a relevant science discipline with master or PHD preferred.

• Knowledge of biologics manufacturing, bioassays, biochemistry, biostatistics and experience within a GMP testing laboratory.

• A clear understanding of working within a regulated environment.

• Excellent communication and presentations skills, both written and oral.

• Strong analytical skills with the ability to plan and schedule workloads.

• Drive, high energy, maturity, and ability to work under pressure and deliver results

So, does this all sound like the right role for you? Then join AbbVie!

Additional Information

AbbVie is an equal opportunity employer and 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.

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