Research Scientist/Associate - Analytical Development

Research Scientist/Associate - Analytical Development

Accord Healthcare

United Kingdom

The Role

As we develop our new Accord Biopharma London business unit at Accord, we’re seeking a number of meticulous and methodical Research Scientist / Associates to support the establishment of our Analytical Development department (focusing on monoclonal antibodies (MAbs) and other therapeutic proteins).

To support the analysis of our Biosimilar products, you may transfer in or develop and qualify methods for the structural characterisation of our protein products and process-related impurities – this may include method transfers to manufacturing sites for lot release assays. You will perform analytical techniques such as Chromatography (HPLC, UPLC, RP, SEC/GPC, SEC-MALS, IEX, Affinity Chromatography), Spectroscopy (UV-Vis), Capillary Electrophoresis, (CE, cIEF, CE-SDS) or Mass Spectrometry – full training will be provided on any methods required for use.

To support the smooth running of the department, you’ll prepare and complete all necessary documentation in a timely manner to ensure our Quality, Data Integrity and GLP compliance systems remain accurate and respond to any QA observations related to our data verification. In addition, you’ll help to prepare SOPs, Methods of Analysis (MoAs), data reports and other documents as required.

Being a small site will allow you to work closely and collaborate with Upstream and Downstream development colleagues to better understand the production processes and our products.

The Person

  • Experience in a protein chemistry/analysis role (e.g. Characterisation, Method Development/Optimisation, Process Analytics, Formulation, QC or R&D) within a biopharma / biotech lab / research lab – university sandwich/placement year considered for the Research Associate Role. The candidate will preferably have experience in GxP (GLP, GMP, GDP), however training will be provided.
  • Experience and good technical knowledge in at least one of the following techniques: Chromatography (HPLC, UPLC), Capillary Electrophoresis (cIEF, CE-SDS) or Mass Spectrometry.
  • Highly analytical with a good attention to detail; can follow instructions closely but can identify when further guidance/work is required.
  • Excellent communication and interpersonal skills (in written and spoken English), you’re confident liaising with all levels of seniority and navigating cultural differences.
  • Team player who can interact well within the team to ensure that project goals are met on time.
  • Good IT and data analysis skills using MS Excel and the ability to learn new systems quickly.
  • Degree / Masters / PhD level qualification in a life science, biochemistry, pharmacy, chemistry, biomedical science or other technical scientific discipline with up to 5 years of experience in relevant role.

Competencies

  • Accord-Individual-Action Oriented
  • Accord-Individual-Drive for Results
  • Accord-Individual-Time Management
  • Accord-Individual-Problem Solving

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