AbbVie QC Analyst (Chemistry) / Laboratory Technician IV
AbbVieWestportUpdate time: January 18,2022
Job Description
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. Want to make a worldwide impact? We offer that Want to join an award-winning team? We offer that too Then join AbbVie! We focus on innovative new technologies, and with our high performing team, we develop and deliver products and processes to support AbbVie’s wider global needs. We are always looking for talented people to join our team and, when we find them, we make it our business to treat them well. We are currently sourcing a QC Lab Analysts to join our team at AbbVie, Westport Co. Mayo, on a fixed-term contract basis. As our new QC Analyst, you will ensure that all raw material, in-process, finished product and method transfer testing is carried out per schedule and records are maintained to appropriate requirements. Working in the quality control labs, you will be equipped with the latest design technology for chemical and microbiological analytical testing to meet customers’ needs. So, are you ready to join the AbbVie team? Then read on Key Responsibilities: Maintain and comply with Laboratory Documentation and Computerized Systems Data Integrity requirements. Understand Regulations and business processes required to maintain Laboratory Data Integrity. Responsible for the timely completion of chemical testing. Ensure that all test equipment is used and maintained correctly. Raise change requests and data verification as assigned. Ensure all in-process sampling and testing is completed on time. Maintain up-to-date, complete and precise records of all tests performed. Adhere to cGMP and GLP requirements. Assist in the resolution of quality problems as required. Develop in-house laboratory procedures as appropriate. Support the transfer of new products. Qualifications So what Education & Experience do you need: You will have a 3rd level degree qualification in relevant scientific discipline with experience using HPLC/GC analytical methods is essential. Relevant industry experience preferred. Good oral, written, and presentation skills Strong analytical skills, ability to analyze data and trends and draw conclusions Do you want to be part of this team? then apply today! AbbVie is 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 Temporary Work 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.

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