Skip to main content

Senior QA Specialist - Biopharma Compliance & Validation

Posted 2 days ago

kbi biopharmaRaleigh (NC)

SENIORITY

Lead

Apply (opens in a new tab)

About the role

KBI Biopharma, Inc. is seeking a Principal QA Specialist in North Carolina to lead compliance review of GMP data, oversee QA activities across analytical and microbial labs, and support product lifecycle and regulatory inspections. The role emphasizes patient safety, regulatory adherence, and cross-functional collaboration. The position requires deep QA/QC and cGMP expertise, with extensive experience in FDA/EU regulations, method qualification, and CAPA processes.

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.

More like this