If you are looking for a company where you can personally advance healthcare and make a difference in peoples' lives with your bold ideas and unique point of view, consider working at Labcorp Drug Development as a Quality Control Analyst - Bioassay CMC
Within the CMC (Chemistry, Manufacturing and Controls) business unit at our site in Harrogate, North Yorkshire, the Bioassay department is dedicated to the development, validation and execution of techniques, such as ELISA & Cell Based Assays
In addition, the department also provides method development, transfer, phase appropriate validation of analytical methods.
We structure ourselves to deliver scientific expertise to our clients; collaborating closely with them to support the development of medicinal products through the drug development process and onto market.
Alongside a host of other duties, you will perform analytical testing using a wide range of techniques for clinical, pre-clinical and commercial studies. Alternative terminologies for QC Analyst include Research Associate, Laboratory Analyst, Analytical Scientist.
Your responsibilities will include
Working as part of a team alongside other QC Analysts and QC Scientists to perform analytical testing on small molecules and large protein molecules using the following analytical techniques: ELISA & Cell Based AssaysData processing and analysis, using the appropriate documentation, with strict adherence to current Good Laboratory Practice (GLP) and/or Good Clinical Practice (GCP)Quality Control review of GLP/GCP analytical data and associated documentationInvolvement with the Quality Management System (QMS) for deviation, change control, lab investigations and associated change actions (CAPA)Study supervision and oversight of client projects at lab level; including organising study files and study data throughout the data life cycle, performing stock checks and ordering consumables/reagents, assisting with writing and updating a variety of documentsWorking with QC Scientists to perform a wide range of analytical techniques in accordance with GLP/GCP regulatory requirements, to undertake data processing, and to deliver client projectsAssisting with the maintenance of laboratory equipment and process improvements
Labcorp is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
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