Regulatory Manager CMC

Apsida Life Science are currently partnered with a well-established but expanding consultancy company who have organically grown year on year since they were founded 10 years ago.

They have a strong client base of pharmaceutical and biotech companies and after a recent influx of projects, they are now looking to take on board a Regulatory Affairs manager. They pride themselves in valuing their employees’ previous knowledge and focus on expanding this by investing heavily in their employee career progression.

Responsibilities

• Work within the pharmaceutical industry, focussing on Chemistry Manufacturing and Control (CMC)
• Translating lab results into Regulatory dossier documents
• Include but not limited to CTD, Module 3
• Prepare and coordinate regulatory submissions
• Review reports on pharmaceutical product and process development

Requirements

• A Life Science degree
• Over 3 years’ experience in Regulatory Affairs or CMC
• Knowledge of analytical procedures, specifications, validation methods, stability testing and process controls
• Eager to learn, develop and succeed
• Ability to handle stringent deadlines

With the hope to grow exponentially, they are looking for candidates eager to develop their current knowledge and expertise. If this opportunity interests you and you would like to find out more information, please contact me directly via this advert or email me on geneva.jones@apsida.co.uk. Equally, you can reach me on my direct number +442038542418.

Apsida Life Science is a specialist recruitment business based in London (UK), Redhill (UK) & Boston (USA) that is dedicated to delivering the best talent to the Life Science industry. We believe there is a gap in the market for a cost effective, high quality and trusted recruitment service that puts the candidate journey at the heart of the recruitment process.