GMP Quality Assurance Director – RNA & ASO meds – Lead a Team of 5-7 ** MA, US

Reference: SWI526

Expiry Date: 31-01-2023

Categories Biotech, Clinical Research, R & D

Salary: On Application

Job Type: Full Time

Middlesex County
United States

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Job Description

My team and I would like to offer you a brand-new position in a R&D biotech company working on early development RNA meds. This is a great opportunity to develop your leading and managing skills as a GMP Director surrounded by pro-active and committed professionals who possess impressive experience in various therapy areas and are all committed to their goal of helping people suffering from rare diseases.

If you are grappling with lack of clarity from your current senior management and/or pipeline, this is the perfect opportunity to join a dynamic and intimate environment with less people to go through, when it comes to bringing your ideas to reality. My client will support you through every step of the way!

To fill the role of GMP Quality Director, our client is looking for someone experienced in supporting technical services and overlooking technical agreements. If you have been responsible for activities like batch release and OOS within the last few years, this is your chance to lead a well-organized team and be recognised for your every achievement in their current P1/2 trials.

Our client is based in Lexington MA, USA and the position comes with a strong package and stock, and my client will also cover any loss of bonus and/or vesting stock due in 2023.


To Apply!

To apply for this role, please contact me, Theo Moore on US 587 216 9302 or my colleague Ivan Nash on US 908 378 8980 or send a full CV to and we will reply by return. We will support you throughout the interview and on-boarding experience.

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