As a leading contract research organization, LabCorp provides comprehensive drug development solutions for a range of industries.
We are a global leader in nonclinical safety assessment, clinical trial testing and clinical trial management services.
Together with our clients, we support the development of innovative, life-changing treatments.
The Role:
Our UK site in York, is currently recruiting for a QC Analyst to join the BioPharmCMC team.
Within the York BioPharmCMC business unit; the Protein Chemistry and Bioassay departments provide dedicated release and stability testing of Small and Large Molecule pharmaceutical products from preclinical through to the commercial phase.
The department provides method development, transfer and 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.
The QC Analyst role within the York BioPharmCMC department is a laboratory scientist position.
Alongside a host of other duties, you will perform analytical testing using a wide range of techniques for clinical, pre-clinical and commercial studies.
Job Responsibilities:
Performing analytical testing on small molecules and large protein molecules using the following analytical techniques:
HPLC, Capillary Electrophoresis, Compendial Techniques, ELISA and Cell Based Assays.
Recording of data on the appropriate documentation with strict adherence to current Good Manufacturing Practice (cGMP).
Quality Control review of GMP analytical data and associated documentation.
Involvement with the Quality Management System (QMS) for deviation, change control, lab investigations and associated change actions (CAPA).
Lab level oversight and organisation of client projects; 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 documents.
Working with QC Scientists to perform a wide range of analytical techniques in accordance with GMP regulatory requirements to deliver client projects.
Assisting with the maintenance of laboratory equipment.
What Labcorp Drug Development can offer you:
A comprehensive onboarding training plan covering laboratory, technical and regulatory training packages.
Unsurpassed career development opportunities, with the ability to develop your technical and managerial skills.
Ability to work with a variety of different clients on wide ranging projects.
Competitive salary dependent on experience, and a comprehensive benefits package including contributory pension.
Key Information:
Position includes a 6-month onboarding & probationary period during which working hours are 8:
45am - 5pm, based at our site in York.
Prerequisites:
Required:
Scientific degree (Biochemistry, Chemistry, Biology, Molecular Biology, Biomedical Sciences etc) OR relevant scientific industry experience.
Required:
Ability to multitask and prioritise workload, with excellent attention to detail.
Required:
Exceptional communication skills.
Required:
Ability to integrate well within an established and fast growing team.
Required:
Computing skills, including word processing and use of spreadsheets (e.
g.
Microsoft Office packages and Microsoft Project).
Desirable:
Previous analytical experience using any of the following techniques:
HPLC, ELISA, Cell Based Assays, Capillary Electrophoresis and compendial techniques.
Desirable:
An understanding of health and safety policies and of GMP/GLP/GCP.
Labcorp is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.
For more information about how we collect and store your personal data, please see our Privacy Statement. Labcorp YorkEngland
