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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 Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn.

#AbbVie Analytical Technology Specialist II

Westport, Ireland Req ID 2202023 Category Quality Assurance Division AbbVie

Unleashing your full potential? We OFFER that.
A career of limitless possibility? 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 an Analytical Technology Specialist II to join our diverse Biologics Development Lab in Westport, Co. Mayo. 
Reporting to the Associate Director of Technical Centre, you will be responsible for various activities such as undertaking analysis of in-process, release, stability and investigational analytical activities. You will work with a dynamic, innovative team in supporting and executing Method Transfers, and Validation activities associated with biological drug product analytical processes. You will also be involved in QMS, compiling and reviewing of Laboratory documentation (e.g. SOPs, methods, Master records, Batch Records, Reports) and carrying out routine lab tasks. 

Is this a team you want to be part of? Then read on…

Key Responsibilities:
•    Conduct in process, release, stability & investigational analytical activities
•    Support and execute method transfers and validation activities
•    Compile and review of Laboratory documentation (e.g. SOPs, methods, validation documentation etc.)
•    Train and mentor new members of the team
•    Support regulatory inspections as required
•    Perform routine lab tasks to maintain a high standard of housekeeping
•    Support laboratory projects to ensure timelines are maintained
•    Ensure all testing is carried out in a timely manner to prevent late testing and delays in manufacturing schedule
•    Participate at meetings and provide input to key projects and improvements within the group

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 bachelors degree in a relevant science discipline with 2-4 years industry experience preferred
•    Experience within a GMP testing laboratory preferred.
•    Working knowledge of QMS (Quality Management System)
•    A clear understanding of working within a GMP, aseptic 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!

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

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