Director/Sr. Director CMC Regulatory Affairs
2 weeks ago
Salary: $175-250k depending on experience Responsibilities:
- Interpret global regulations and guidance to identify risks and provide strategic guidance to cross functional product teams.
- Develop CMC regulatory strategy for early-stage cell therapy products through late stage and product registration.
- Represent CMC regulatory affairs on product teams and in health authority interactions.
- Lead development and compilation of Quality modules for global regulatory submissions including but not limited to clinical trial applications, health authority responses and briefing packages.
- Ensures that submission documents and correspondence are of the highest quality in terms of content, organization, clarity, and accuracy.
- Lead the build out CMC regulatory organization to support expanding cell therapy pipeline.
- Serve as a strong partner to the Development and TechOps organizations.
- Perform other duties as required.
- Hire, lead, managing workflow and develop of staff.
- Demonstrated ability to develop/maintain strong working relationships with the cross functional teams, participate on and/or lead multi-functional teams, manage/prioritize multiple projects, and work independently.
- Advanced leadership skills to successfully lead complex programs. Able to effectively build and lead high-functioning teams.
- Outstanding organizational skills with the ability to multi-task and prioritize.
- BA/BS degree in life sciences required
- 8-10 years of experience in CMC Regulatory Affairs
- Experience in cell therapy preferred
- Knowledge of global CMC regulations
- Experience leading CMC teams in IND, IMPD, BLA, MAA filings
Please send resumes to gavin@biophaseinc.com and visit our website at www.biophaseinc.com for additional job opportunities
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