Primary responsibilities: Regulatory CMC for manufacturing and QA/QC activities in drug development.
Responsibilities include regulatory strategy and submissions.
Specific responsibilities not listed in the description.
Day-to-day management of regulatory CMC activities.
Collaboration with manufacturing and quality teams.
Preparation of regulatory documentation and filings.

🎯 Requirements

Minimum education required
Relevant experience
Experience in biotech or pharma industry
Skills
Behavioral competencies/licenses
Travel required if applicable

🎁 Benefits

Market-leading compensation
401(k) with employer match
Employee Stock Purchase Program (ESPP)
Pre-tax commuter benefits
Referral bonus
Subsidized lunch and parking

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