We're looking for a Regulatory Associate I, working in the Biotechnology/Medical Devices industry in South San Francisco, California, United States.
Ensures that the quality, content, and format of regulatory submissions comply with applicable regulations and guidelines
Provides support to the TRTs and facilitate authoring, review and adjudication of regulatory submissions and handle communications with stakeholders
Perform regulatory compliance activities such as submission of BPDRs and Inspection responses.
The pay range we're offering is 25 - 30 per hour. This position may present an opportunity to go permanent.
Our client is an award-winning clinical development company. Improving lives globally with 20+ years’ experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.
Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.
Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.
Experience Required for Your Success
Pharmaceutical experience in particular in regulatory or GMP compliance is a plus
What Do You Think?
Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible? Apply here.