About AbbVie AbbVie’s mission is to discover and deliver innovative medicines 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, eye care, virology, women’s health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Challenging work with a global impact? We OFFER that. A rich innovative pipeline? We OFFER that too. Welcome to AbbVie! At AbbVie, we offer you the resources and a global reach to empower your innovative mindset. From day one, we’ve known it takes teamwork and collaboration to develop the scientific breakthroughs, innovative pipelines, and therapies that change millions of patients’ lives around the world. In short, we know it takes “you” to make those ground-breaking advancements happen. We take pride in serving and supporting our communities and protecting the environment, making a lasting impact that's felt within healthcare and beyond. We are now recruiting a Data Analytics Specialist to join our diverse Biologics- Bioassay Laboratory team in Westport, Co. Mayo. In this role, you will be responsible for the monitoring and trending of all Cell Based Potency Assay (CBPA) outputs, including the Drug Substance potency performance, to ensure that the CBPA method and the Drug Substance are performing optimally. As part of your role, you will present trending outputs to both the Bioassay and QA Departments while identifying and recommending plans of action in response to any adverse trends or trends that have potential to impact method robustness. So let’s tell you a little more about this role… In your new role, you will: Perform daily trending of commercial Cell Based Potency Assay outputs Establish tracking, qualification, and implementation strategy to CBPA critical reagents Maintain “live” monitoring and trending data sets for CBPA methods and for Drug Substance performance CBPA analysis of release, stability, and investigational analytical activities while supporting analytical assessments associated with Method Transfer and Validation activities associated with key biological drug product projects Support regulatory inspections as required Drive Root Cause Analysis investigations Qualifications So does this role sound exciting? then read on..... Qualifications To succeed in this role, you will have the following Education and Experience: • BS.C or Master’s Degree or Ph.D in Biological Science or Bioinformatics/Biostatistics • Knowledge of biologics manufacturing, bioassays, biochemistry, biostatistics, and experience within a GMP testing laboratory. • Clear understanding of working within a regulated environment with a keen interest in data and the impact it can have on decision making, continous improvement and building future success So, does this all sound like the right role for you? Then join AbbVie! As an Equal Employment Opportunity Employer; we value bringing together individuals from diverse backgrounds to develop innovative solutions for patients and being part of an inclusive work environment. Travel No Job Type Experienced Schedule Full-time Job Level Code IC Equal Employment Opportunity At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis 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, protected veteran status, or any other legally protected characteristic.