Quality Assurance Specialist



Are you looking for a fast paced position in a rapidly growing Analytical Chemistry Laboratory? We are currently seeking to fill a variety of positions at our Ann Arbor, Michigan facility. We are searching for talented and motivated individuals that would enjoy working in a team oriented, entrepreneurial company.

Avomeen is part of the CRO industry, which serves Pharmaceutical, Biotech, Legal, Automotive, Paints & Coatings, and other diversified industries with laboratory services.  This $600B dynamic industry has risen to fill the needs of a wide variety of companies that have realized that Analytical Science is not core to their mission and is better done in an outside science based organization that values and supports it.

At Avomeen we:

  • Perform analysis to get approvals for innovative as well as generic pharmaceuticals
  • Perform testing as well as Expert Witnessing for Law firms to support litigation
  • Re-engineer and improve existing products for new markets and applications
  • Invent new products (several clients have appeared on Shark Tank)
  • Solve major quality problems for manufacturers including soft drink companies, auto manufacturers, pharmaceutical manufacturers, and others

If you are interested in the job opportunity below, please forward resume, cover letter, and salary history to hr@avomeen.com.

About the Opportunity

We are looking for a talented individual to fill a Quality Assurance Specialist position at our Ann Arbor, MI facility.

In this position, you will be responsible for:

Auditing laboratory work to GMP standards by reviewing compliance to SOPs. This position reports to the Manager of Quality at Avomeen.   This is an entry level position for a recent graduate in the sciences that is seeking a non-laboratory opportunity.  The position will involve training to develop the right candidate into a Quality Professional.

Position Summary Responsibilities: 

  • Manage laboratory accreditation applications and renewals including DEA licensing and ISO registration
  • Perform and review internal audits of the laboratory quality program
  • Review and revise Standard Operating Procedures
  • Audit laboratory compliance to Standard Operating Procedures
  • Monitor compliance to completion of laboratory investigations and corrective and preventative actions
  • Coordinate and respond to regulatory, client, and third party quality assessments
  • Coordinate document and record control
  • Audit and approve project work for compliance to company SOPs as well as GMP requirements
  • Other duties and responsibilities may be required as needed

Desired Qualifications: 

  • B.S. in a scientific discipline, preferably chemistry or biochemistry
  • 0-3 years experience, contract lab experience a plus.
  • A highly motivated self-starter that can work with minimal supervision

Work with us to make health & medicine better for everyone.

Start a quote or ask an experienced scientist today.