Senior Biologics CMC Regulatory Affairs Consultant

Posted yesterday

precision pointLos Angeles (CA)

Regulatory Affairs Specialists Research and Development in Biotechnology (except Nanobiotechnology)

SENIORITY

Senior

Apply

About the role

Precision Point seeks a Regulatory Affairs CMC Consultant to lead CMC authoring, strategy, and lifecycle management for a biologics pipeline. This hands-on role requires setting regulatory strategy and performing technical writing without a team. You will report to the RA CMC Executive Director and collaborate with Analytics, Quality, Manufacturing, and external CMOs to ensure submission readiness and inspection-ready documentation.

Before you apply

Applying takes about a minute. These four things decide how fast it moves after that.

Your profile is current

It's what we read first. Occupations, seniority and locations matter more than a long history.

Two examples you can talk through

Not a portfolio — just two pieces of work where you can explain the decisions and what you'd change.

A number in mind

What you're on now and what would make you move. We negotiate better when we know both.

Your notice period

Employers plan around it, and it's the question that stalls offers most often.

Once you apply, someone reads it and calls you before anything reaches the employer — usually within two working days.