Job Opportunities

At QSC we work with our clients on complex Regulatory and Quality solutions in the Life Sciences Industry. Our seasoned professionals bring about a positive change for our clients.

If you are a Regulatory and/or Quality compliance professional or possess a scientific/technical background in the Pharmaceutical, Biotech, or Medical Device industry and would like to be considered for a consulting position with QSC, please submit your resume.

Current Available Positions

  • GLP Bioanalytical Consultant

    Scope of Work: Audit Bioanalytical Study reports and data to ensure that the analyst followed SOP’s and investigations/deviations were appropriately documented. Based on the findings the consultant will need to work with client to write investigation documentation, correct Bioanlaytical study report if needed, and work with team to implement corrective actions.

    Consultant will need to have a Bioanalytical/GLP background. experience with LC/MS/MS and good technical writing skills.

    Duration: ~6 months
    Location: Northeast United States
    • Clinical Quality Consultant

      Scope of Work:  The Senior Quality Manager of Quality Assurance (QA) GCP is an independent contributor who is responsible for performing quality assurance activities to ensure that client clinical trials are conducted in accordance with Good Clinical Practice guidelines, applicable regulations and Client policies and procedures.  In addition, this position is responsible for adhering to the Client’s quality standards as set forth in the Quality Management System. The Senior Quality Manager is also responsible for accurately identifying and communicating compliance risks and overseeing action plans to mitigate risks.

      Consultant will need to have relevant GCP experience with knowledge of FDA regulations, EU directives, MHRA Statutory Instruments and ICH guidances. 

      Duration: ~3 - 6 months 
      Location: Northeast United States