GMP Auditor (Freelance)
- Location
- Raleigh, NC, United States
- Work mode
- Remote
- Employment type
- Full-time
About the job
Company Description Medicine moves forward here. So will you. ADAMAS Consulting helps the world's pharmaceutical and biotechnology companies uphold the highest standards of quality, compliance and patient safety. Since 2007 we have partnered with organizations across GCP, GVP, GMP, GLP and Computer Systems Compliance, and we are trusted by many of the most respected names in life sciences. We think of our work as more than auditing. At its best it is intelligence: helping clients see the compliance risks that matter most and prevent the problems that could put patients at risk. That takes sharp, independent thinking and deep expertise, which is exactly what our people bring.
Job Description
- Planning, preparation, conduct, reporting and follow up of various types of GMP audits according to expected quality and timelines
- Executing audits based on a comprehensive understanding of all regulatory requirements and Good Manufacturing Practice (GMP)
- Performing GMP quality assurance projects on behalf of client companies within the pharmaceutical/biotechnology industry.
Qualifications
- Experience in conducting and leading internal and external GMP audits for a variety of stakeholders
- Experience in conducting a range of service provider audits would be an advantage (e.g., API manufacturers, CMOs)
- Experience in coordinating and managing inspection preparation activities for GMP process inspections both at the sponsor and investigator site.
- Experience and full understanding of current applicable regulatory standards.
- Expert knowledge of national and international GMP legislation and guidelines
- Proficient in managing projects and ensuring deliverables are provided in a timely manner
- Ability to identify issues and offer solutions in a pragmatic way
- BS in Life Science preferred
- Up to 40% travel and ability to conduct remote audits
Additional Information Why ADAMAS? When you join Ergomed Group, you make a difference by helping to bring safe and effective pharmaceutical treatment to patients around the world. You’ll join a passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting. We are diverse in many ways, yet our values unite us. Our values are how we work, not words on a wall. If they sound like you, you will feel at home here.
- Quality: we hold ourselves to the standard patients deserve.
- Integrity and trust: we do the right thing, especially when it is hard.
- Drive and passion: we care about the outcome, because someone is waiting on it.
- Agility and responsiveness: we move quickly, because patients cannot wait.
- Belonging: everyone is welcome, and every voice counts.
- Collaborative partnerships: we go further by going together.
We look forward to welcoming your application.
From Ergomed's careers page (SmartRecruiters), checked 29 Oct 2026.
How to apply
- Select Apply on jobs.smartrecruiters.com. It opens Ergomed's own application form in a new tab, run on SmartRecruiters.
- Fill in the form and upload your résumé there. Jobiwork never sees your application.
- Ergomed will reply to you directly. No real employer asks you for money to apply.
Posted 10 Sept 2026 · checked 29 Oct 2026 · Report this job