Our Life Sciences group specializes in assisting Pharmaceutical, Medical Device and Biotech clients with highly skilled professionals within the areas of Quality Assurance, Validation, Clinical and Regulatory Affairs. We have a database of consultants within the New England area as well as nationwide.

Life sciences Industry is continually evolving, spurred by complex and wide-ranging issues such as industry consolidation, cyber-security, compliance, emerging markets, and economic uncertainty. It’s not just your products that will help you stay ahead of the competition – you need to invest in your people. Talent strategy must be inextricably aligned with business strategy, with the right people in the right places doing the right things – at the right value.

Our Life Sciences and Technology group is dedicated to supplying the quality, safety, validation, clinical, regulatory and compliance experts that ensure that our clients’ medical devices, medicines, delivery systems and therapeutic products are the safest and most reliable in the world. Within this technology segment, Agile Workplace Staffing has rigorously and persistently sought out and recruited the most highly-specialized and proficient talent nationwide making it uniquely qualified to respond quickly and confidently to client’s critical resource needs.


  • Quality Assurance, Quality Control & Quality Systems
  • Quality Remediation, Gap Assessment & Quality Investigations
  • Risk Management
  • Post-Market Surveillance
  • Design Control
  • Process Development & Engineering
  • Internal & External Auditing
  • Compliance Engineering (US/International)


  • Validation Engineering, Documentation Development and Execution
  • Facilities, Utilities, Equipment, Process, Automation, Test Method, Analytical Method, Laboratory, Computerized Systems, Software, & IT Validation
  • Cleaning & Sterilization; Packaging & Labeling


  • Regulatory Submissions, Technical Writing & Regulatory Strategy Development
  • PMAs, 510(k)s, NDAs, ANDAs, BLAs, INDs, IDEs & other regulatory filings
  • International Regulatory Filings, Product Registrations & Labeling


  • Medical Writing
  • Medical Monitoring
  • Clinical Trial Management
  • Clinical Development / Clinical Study Design
  • GCP Auditing
  • Drug Safety / Pharmacovigilance
  • Biostatisticians, Toxicologist & Clinical Scientists

Industries Served