Industry

Life Sciences

Consultants for medical device and pharmaceutical teams

Regulated work needs people who already know the regulations. We place quality, regulatory, validation and R&D consultants who have delivered inside FDA- and ISO-governed environments.

Roles we staff

  • Quality engineers and quality managers
  • Regulatory affairs specialists
  • Design controls and risk management
  • CAPA and complaint handling
  • Software design life cycle (IEC 62304)
  • Validation (CSV, process, cleaning)
  • Internal and supplier auditors
  • Clinical and manufacturing support

Where we work

  • Medical devices
  • Pharmaceuticals
  • Diagnostics
  • Combination products

How an engagement works

  1. Scope the role. A 20-minute call to understand the project, skills and timeline.
  2. Review candidates. Screened, reference-checked consultants, usually within days.
  3. Start the work. We handle onboarding, payroll and compliance so you can focus on the project.

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