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.
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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 â€� immunology, oncology, neuroscience, and eye care â€� and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at . Follow @abbvie on ,Ìý,Ìý,Ìý,ÌýÌý²¹²Ô»åÌý.
At ourâ€�Westport site in Co. Mayo, we are now hiring anâ€�Analytical Technology Specialist to join our talented and ambitious team, on a 12 months fixed term contract.Ìý
The role centers on conducting Cell-Based Potency Assay (CBPA) testing, ad-hoc investigational & development testing.Ìý
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.Ìý
So if you are interested in joining this team, read below to find out more…�
In your new role, you will:Â
- QC Testing of commercial product via Cell Based Potency Assay and related ELISA methodsÂ
- Routine lab duties including critical reagent qualifications, inventory management and equipment maintenanceÂ
- Interdepartmental co-ordination - support product release, drive completion of defined projects etc.Ìý
- Support and execute Method Transfer and Validation activities associated with key biological drug product projects.Ìý
- Assay performance monitoring and trendingÂ
- Compiling and review of Laboratory documentation (e.g. SOPs, methods, validation documentation etc.).Ìý
- Perform lab duty tasks to maintain a high standard of housekeeping within the laboratory.Ìý
- Support regulatory inspections as required.Ìý
- Supporting Root Cause Analysis InvestigationsÂ
- Adhere to and support all EHS procedures and policies.Ìý
- Support and lead Laboratory projects to ensure timelines are met successfully.Ìý
To succeed in this role, you will have the following Education and Experience:Â
- Bachelors of Science, Master’s Degree or Ph.D in a Biological ScienceÂ
- Practical experience of mammalian cell culture and basic techniques (Passaging, freeze-down, drug treatments) is an advantageÂ
- Previous GMP experience is advantageous but not essentialÂ
- Sound scientific/practical understanding of ELISA based methodsÂ
- A clear understanding of working within a regulated environment.Ìý
- Excellent communication and presentations skills, both written and oral.Ìý
- Strong analytical skills with the ability to plan and schedule workloads.Ìý
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.â€� Equal Opportunity Employer/Veterans/Disabled.Ìý
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