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 (https://www.tiktok.com/@abbvie) . Job Description At our Westport site in Co. Mayo, we are now hiring an Analytical Technology Specialist II to join our talented and ambitious team. The Role of Analytical Technology Specialist II involves performing analysis of in-process, release, stability, and investigational analytical activities of NPI samples. They are responsible for the completion of write-ups in a timely manner and the review of other analysts work. Other aspects of this role are QMS, Instrument validation, compiling and review of Laboratory documentation (e.g., SOPs, methods, Master records, Batch Records, Reports), performing Stability sample pulls and carrying out routine lab maintenance tasks. Are you intrigued? Do you want to learn more? A snapshot of your key responsibilities as a Analytical Technology Specialist would be: + Performing In process, release, stability, and investigational analytical activities, completion of write-ups and review of other analysts work, Lims data entry and validation. + Carrying out training with new members of the group. + Leading the Validation activities for new instruments. + Adhering to and engage in all Lab Safety rules, programs and initiatives. + Compiling and reviewing of Laboratory documentation. + Supporting regulatory inspections as required. + Performing routine lab tasks to maintain a high standard of housekeeping. Qualifications + 3rd level qualification in a relevant Science discipline + Minimum 2 years’ experience in a regulated GMP Pharmaceutical environment + HPLC experience with Empower Software essential (1-2 years min), biological analytical techniques desirable + Excellent communication and interpersonal skills for interaction with internal departments (QA, Validation, IS, EHS) + Proven ability to troubleshoot and problem solve. + Able to work in a fast, dynamic, environment whilst being able to adjust readily to meet unexpected constraints 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