Start Date
Immediate
Expiry Date
03 May, 25
Salary
0.0
Posted On
23 Feb, 25
Experience
5 year(s) or above
Remote Job
Yes
Telecommute
Yes
Sponsor Visa
No
Skills
Good communication skills
Industry
Pharmaceuticals
HOW TO APPLY:
If you possess the experience, passion and ability to make this role a success then we would like to hear from you. Please click on the ‘apply’ button to submit your CV / Cover Letter. The closing date is 4th March 2025. For more information, you can contact us on: careers@accord-healthcare.com
A Bit About Us:
Accord Healthcare Europe is one of the fastest growing pharmaceutical companies in Europe. Accord has one of the largest market footprints of any European generic and biosimilars companies selling generic medicines in over 80 countries around the world. This global footprint enables us to deliver vital, affordable medicines to national health systems supporting healthcare professionals to transform patient lives worldwide. The approach of Accord is agile and inventive, always seeking to improve products and patients’ access to them. Accord are driven to think differently and deliver more for the benefit of patients worldwide.
To continue our growth, we’re looking for the best and brightest technical minds and forward-thinking business professionals. Keeping our people at the heart of all we do, we offer rewarding opportunities for those looking for continued personal and professional growth, investing in training and development tailored to each individual’s focus. So, if you’re looking for an inclusive company to take your career to the next level, you’re certainly in the right place; come and join us to make it better.
Job Types: Full-time, Permanent
Additional pay:
Benefits:
Schedule:
Ability to commute/relocate:
Work Location: In person
Application deadline: 04/03/202
As we develop our Accord Biopharma London business unit at Accord, we’re seeking a meticulous and methodical Research Scientist 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.