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Contract: W2 role, Full time
Closing Date: 30/06/24
G&L is currently looking for experienced Regulatory Affairs CMC professionals to join our ATMP team in North America.
This role will include the development and maintenance of the Quality sections of regulatory submissions to support Cell Therapy products.
You will be tasked with a wide variety of responsibilities including building Clinical trial applications, New marketing applications, HA responses & background packages, and post-approval submissions.
G&L has various projects across 2024 and we would like to hear from professionals who are planning a career move and would like to explore options.
Typical duties will include:
Our ideal candidate would have:
G&L Consultants are known for being strong team players, who are confident to communicate their opinions, facts, and thoughts with clarity, transparency, and honesty.
We have high expectations of our colleagues, and our clients expect outstanding standards – both with results that are achieved, and also by looking for opportunities for continuous improvement.
You should be open-minded and agile – be interested in other’s opinions, and ready to act on new information and differing perspectives.
For further details, please send your CV to: talent@gandlhealth.com
G&L Healthcare Advisors is an equal opportunities employer and welcomes applicants from all sections of the community regardless of their gender, religious belief, political opinion, sexual orientation, disability, age, marital status, or race.
We recruit based on talent alone and firmly believe that an individual’s background should play no part in the recruitment and selection process.
G&L is committed to everyone having the right to work in an environment free from threat of discrimination, intimidation, harassment, and abuse. All employees at G&L share the responsibility to challenge discriminatory behavior and promote equality of opportunity.
Full Time
$77k-102k (estimate)
05/02/2024
07/01/2024