Company DescriptionAbbVie'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 DescriptionYou’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 New Product Introduction team, on a 12 months fixed term contract.The NPI group is responsible for releasing and stability testing products in development after the transfer and validation of the assay from the Product Development Science and Technology team.The role centers on supporting new product introduction testing, conducting Cell-Based Potency Assay (CBPA) testing, ad-hoc investigational & development testing. There may be a requirement to execute or assist on new method transfers and validations.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.In your new role, you will:Support NPI QC Testing on PSBs, Clinical, PPQ, Demo and investigational lots via Cell Based Potency Assay and related ELISA methods.Timely review of testing records and all associated documentation.Routine lab duties including critical reagent qualifications, inventory management and equipment maintenance.Perform all activities in line with regulatory (QA and EHS) and corporate requirements.Open and progress QMS records as required – Laboratory Investigations, Change Controls.Complete assigned training on time.Understand regulations and business processes required to maintain laboratory data integrity.Provide input on assay performance monitoring and trending.Support Root Cause Analysis Investigations.Attend departmental and Tier meetings.QualificationsTo succeed in this role, you will have the following Education and Experience:Bachelor’s of Science, Master’s Degree or Ph.D. in a Biological Science, 1–3 years QC GMP experience.Practical experience of mammalian cell culture and basic techniques (Passaging, freeze-down, drug treatments) is an advantage.Sound scientific/practical understanding of ELISA based methods.A clear understanding of working within a regulated environment.Excellent communication and presentation skills, both written and oral.Strong analytical skills with the ability to plan and schedule workloads.Additional InformationAbbVie 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.htmlUS & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html
#J-18808-Ljbffr