Job Description

We are excited bring this new opportunity to your attention! Our client is a growing  clinical stage company committed to bringing innovative genetic medicines to market,  to treat rare and debilitating neurodegenerative diseases.  They are looking for a  QA GMP Director to handle the growing QA function at their in-house R&D site in Massachusetts, and  to support various NMEs in mid and now late-stage development (P2/3), through  1^st registration and then commercialisation.

This exciting new role was created due to the growth of the organisation and also a number of internal promotions.  Your responsibilities and input will grow in a number of areas, as new products continue to move through the pipeline, and you will lead, manage and mentor an experienced and capable team covering a  varity of activities as the QA function continues to grow to meet the new demands of an expanding organisation.  You will face new challenges in an evolving role that will make this position varied and interesting. 

Your line manager has held positions of increasing responsibility in global manufacturing environments, through all stages of development for small molecules, biologicals and now for Cell and Gene Therapy products, and she has countless significant contributions to her name.

Our client has a one-of-a-kind discovery and development platform that allows the organization to identify novel oligonucleotides and the organization is led by an impressive ex big pharma senior executive leadership team, comprised of skilled, knowledgeable, and dedicated professionals committed to their patients and colleagues. The company culture is very welcoming of all newcomers, and it will not take you long to be immersed in their friendly and collaborative environment.

If you have overseen CAPA and deviation activities and provided direction and support of investigations within the last few years, this is your chance to lead a well-organized and growing team (of 5-7)  for a company moving into Ph. 3 and towards its first NDA preparation, and ultimately commercialization.

If you are interested in hearing more about this opportunity, my team and I would be happy to present you with more information! Our client is offering a very competitive package with a strong salary, generous bonus, and excellent LTIs/stock plan.

To Apply!

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

GDPR & Data Protection: Your information is safeguarded for GDPR, and you will have the right to edit, amend or delete and ’’be forgotten’’ at any time after your initial registration.”