Senior Associate, US Regulatory Affairs
Employment type
Full-time
Work setting
On-site
Location
Emeryville, CA
Schedule
Day shift
Posted
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Job overview
The Senior Associate, US Regulatory Affairs is an onsite role based in Emeryville, CA, managing regulatory projects. Compensation is not specified in the posting. This role plans and coordinates regulatory submissions to ensure compliance with company goals and FDA requirements. The associate assists cross-functional teams with regulatory strategy and prepares documentation for product registration.
What you'll do
- Plan and manage regulatory activities
- assist in developing regulatory strategies
- prepare and submit regulatory dossiers
- ensure compliance with requirements
- participate on project teams
- maintain regulatory knowledge.
What we're looking for
- Skills & competencies
- full-timeday shiftemeryville caregulatory affairspharmaceuticalfdacomplianceindonsiteno on-call
- Work arrangement
- Weekend coverage required
Benefits & perks
- Equal Opportunity Employer.
Why this role
Requires 2+ years of experience in the pharmaceutical industry and knowledge of INDs.
About the employer
BeOne Medicines is hiring for this role. Industry: Pharmaceutical Preparation Manufacturing. Sector: 32.
Additional details
- Industry sector
- 32
- Industry
- Pharmaceutical Preparation Manufacturing
- Occupation code
- 13-1041.07
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Listing ID: d3994312-1d02-474e-adf9-ca91433a9bfa