Life Sciences staffing
Quality, regulatory, data, and validation talent for pharma, biotech, and medical devices.
In life sciences, the product is only half the work — proving it, documenting it, and keeping the systems that touch it validated is the other half. That second half is where staffing gets specialized fast: a QA specialist who has lived inside GxP, a CSV engineer who can defend a validation package, a clinical data manager who knows what an auditor will ask.
PEXIVA Workforce recruits for that documentation-grade rigor. Screening covers not just the skill but the regulated-context fluency — GxP awareness, audit experience, and the writing discipline the industry runs on.
Role families we place
- QA/QC specialists and quality engineers (GxP environments)
- Computer system validation (CSV) and CSA engineers
- Regulatory affairs and submission support
- Clinical data management and biostatistics support
- Lab informatics (LIMS/ELN) analysts
- Manufacturing and packaging operations support
Engagement models
Contract for validation and submission pushes, contract-to-hire for quality teams, direct hire for regulatory leadership.