A Career Opportunity with ADAMAS Consulting

This is an immediate, full-time employment opportunity for an ambitious individual who is looking to serve as an industry expert, gain international experience and broaden their skills while being home-based in the United States.

ADAMAS Consulting is a leading Quality Assurance Consultancy with offices in the UK, India and United States. We provide a range of independent QA services to the pharmaceutical industry.

Our Mission is to be the provider of choice for truly global Quality Assurance Services to the pharmaceutical and biotechnology industries, by adding value through the efforts of our dedicated, highly experienced, highly trained and motivated team.

We are currently looking for a GxP Auditor with the following attributes:

  • BS or equivalent in a life science
  • A minimum of five years QA experience
  • Experience at conducting GCP Investigator Site Audits required
  • Good knowledge of international regulatory requirements and industry guidelines governing global GCP (ICH, EMA, FDA) required
  • Knowledge and experience of other GxPs (GLP, GMP) preferred
  • Registrations, accreditations or certifications preferred (e.g., RQAP-GCP)
  • Ability to identify issues and offer solutions to problems in a pragmatic way
  • Good attention to detail, with the ability to see the ‘big picture’
  • Highly professional and self motivated, experience working from home
  • Ability to assimilate and analyse information rapidly
  • Confidence to work alone or in a team

ADAMAS’s success is down to the calibre of its people – to reward them we offer a competitive salary with benefits, excellent working conditions, and a fulfilling and rewarding career, with plenty of opportunities for further development.

So, if you like the prospect of flexible working conditions, domestic and international travel (approximately 50%) and opportunities to further develop your skills and knowledge, then please submit your CV to: Karen Andrews, Operations Assistant karen.andrews@adamasconsulting.com

The ADAMAS Corporate Brochure 2016


Brochure – Please download the ADAMAS brochure describing our QA services and contact details.

Regulatory Environment


The development of medicines is the most regulated industry in the world, and compliance at each stage of the research and development process, as well as after licensing, is critical to ensuring high quality and safe medicines reach patients in a timely manner.



ADAMAS’s consultants have expertise across the G’X’Ps in pre-clinical, clinical and post-licensing areas. They have worked across many different therapeutic areas and product types including oncology, vaccines, biologics, medical devices and gene therapy. As a company we have developed close partnerships with our clients to support them in their development programmes and post-licensing activities, and to guide them successfully through their worldwide regulatory inspections.


How to be a Clinical Auditor


‘So you want to be a Clinical Auditor?’, an article written by CEO Dr. Patricia Fitzgerald.

Benchmarking Data


Please download our benchmarking data sheet, to see how these data compare with your own performance. To discuss a more detailed report, or analysis of a data subset, please get in touch.

Is your QMS compliant?


Is your QMS compliant to the upcoming ICH E6 Addendum? Download our 5-point checklist

ICH (E6) R2 Addendum - Step 4


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