Associate Director CMC

ARM Life Sciences are currently partnered with a leading Consultancy business based in Marlborough, Massachusetts. They are a specialist growing consultancy firm providing industry leading services within CMC.

We are currently looking for an Associate Director of CMC to join them on a permanent basis providing support for their clients in and around the Massachusetts region. You will be working with a combination of global businesses and niche seized organizations undertaking both operational and strategic project work within CMC.

To be consider for the role you must have the following –

- Aspiration to be driven to learn and apply scientific principles to solve CMC technical and project management challenges.

- 6-10 years of experience in Regulatory Affairs in a Pharma, Biopharma setting.

- Understanding of ICH, FDA and relevant CMC/Quality documentation

- Dynamic background to solve CMC challenges

- Adept in developing risk based CMC strategies in line with new initiatives

Other key area of the role are as follows –

- Knowledge and experience in pharmaceutical development, manufacturing and testing (combination of drug substance, drug product development or analytical/quality control)

- Ability to take ownership and responsibility of a set project

- Strong appreciation for science-based CMC development

- Comfortable and confident in presenting ideas to large audiences and in smaller client settings.

This opportunity will be looking to pay $160,000 - $200,000 annually plus bonus and benefits. If you are interested in hearing more please contact Vik Patel on 00442392 458031 or email me on vik.patel@arm.co.uk