QC Analyst

LabCorp

View: 106

Update day: 11-06-2024

Location: Harrogate Yorkshire and the Humber

Category: Pharmaceutical / Chemical / Biotech Science Labor

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Job content

Job Overview:

Are you a recent scientific graduate looking for your first role in industry or an experienced analyst looking for their next step?

Do you want to be a part of the world’s leading drug development company?

Are you looking for a role with training and career progression opportunities?

At Covance by Labcorp in Harrogate, North Yorkshire we are looking to recruit a Laboratory Analyst to join our expanding team.

The CMC (Chemistry Manufacturing Controls) division provides end-to-end analytical solutions and testing services to ensure quality control of our clients manufactured drug products.
We work with leading pharmaceutical and biotech clients to ensure that their manufactured drug product or API (Active pharmaceutical Ingredient) passes all quality testing. Once this testing is complete, it brings our clients one-step closer to successfully launching that drug product on the market; helping bring medicine to patients.

Job responsibilities include:
  • Performing analytical testing on large protein molecules (e.g. monoclonal antibodies, ADCC, biosimilars etc)
  • Working with Quality Control Scientists to perform a wide range of analytical techniques in accordance with GMP regulatory requirements to deliver client projects
  • Working as part of a larger team to ensure that our clients’ molecules pass quality control testing in the timeframe allocated
  • Using the following analytical techniques:Capillary Electrophoresis, Isoelectric Focusing, Mass Spectrometry, BioAssays – ELISA & Cell Based Assays & Pharmacopoeial Methods to deliver client projects
  • Data processing and working on process improvement projects for the division

What Covance can offer you:
  • Competitive salary and a comprehensive benefits package, including health coverage and contributory pension
  • Ability to work with a variety of different clients on wide ranging projects
  • Flexible working and career development opportunities

Education/Qualifications:

  • Scientific degree (Biochemistry, Chemistry, Biology, Molecular Biology, Biomedical Sciences etc.)
  • OR relevant scientific industry experience

Experience:

  • Some previous analytical experience is desirable but not essential
  • An understanding of health and safety policies and of GMP/GLP/GCP
  • Ability to multitask and prioritise workload, with excellent attention to detail
  • Exceptional communication skills
  • Ability to integrate well within an established and fast growing team
  • Computing skills, including word processing and use of spreadsheets (e.g. Microsoft Office packages and Microsoft Project)
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Deadline: 26-07-2024

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