Title: Director/Senior Director, CMC Regulatory Affairs
Reports To: Vice President, CMC Regulatory Affairs
Location: Redwood City, CA
Classification: Exempt
As the Director/Senior Director, you will develop and implement robust regulatory CMC strategy that align with Clinical, Technical Operations, and Quality functions. You will be responsible for high quality submission packages within target timelines.
Job Responsibilities:
- Leads the development and implementation of CMC regulatory strategy for programs in early-/mid- development stage, in preparation of licensure.
- Actively seeks out regulatory knowledge and incorporates this knowledge into submission planning and execution. Stays current with regulatory requirements.
- Proactively identifies regulatory risks and regulatory opportunities.
- Contributes to the appropriate execution of CMC regulatory strategy, including authoring regulatory documents (e.g. IND/BLA sections and meeting packages).
- Operates with effectiveness across functions.
- Builds and manages relationships through active partnering with key internal and external stakeholders.
- Ensures CMC dossiers meet format and content requirements, as well as specific local requirements of individual countries.
- Analyzes and exercises judgment on complex issues, guided by a thorough understanding of CMC.
Skills and Requirements:
- Bachelor's Degree in a relevant scientific discipline, advanced degree preferred.
- Minimum 8 years of relevant experience in CMC Regulatory Affairs.
- Experience in biologics drug development and license applications.
- Demonstrated track record of successful submissions to FDA and/or other health authorities
- Ability to apply scientific principles to assess regulatory issues, request and collect relevant information, analyze data, establish facts, and draw valid conclusions.
- Excellent interpersonal, verbal, and written communication skills as well as the ability to effectively lead and influence others are essential in this collaborative work environment.
- Comfortable in a fast-paced small company environment with minimal direction and able to adjust workload based upon changing priorities.
The Base Salary Range for this position is $190,000 - $260,000. Coherus considers various factors, including professional background and work experience, when determining base pay. These considerations mean actual compensation will vary.
Coherus provides equal employment opportunities to all employees and applicants for employment and prohibits unlawful discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. We also prohibit discrimination based on the perception that anyone has any of these characteristics or is associated with a person who has or is perceived as having any of these characteristics.
** We are currently not accepting any unsolicited resumes from recruiters or employment agencies. **
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What We Do
Coherus is a commercial-stage biopharmaceutical company focused on the research, development, and commercialization of innovative immunotherapies to treat cancer and the commercialization of our portfolio of FDA-approved therapeutics. We are building a leading oncology company backed by in-house expertise and an established infrastructure from our diversified portfolio of FDA-approved biosimilar products. If you are interested in joining a highly innovative and exciting company, please visit our careers webpage at http://www.coherus.com/careers/ for a list of career opportunities
