Validation Supervisor, Technical Operations - Self Care (FIXED TERM- 12 MONTHS)
Core
Lead validation programs for manufacturing, packaging, and cleaning of pharmaceutical products (liquids, solids, semi-solids) to ensure compliance and operational efficiency.
Role type
Senior IC Validation Supervisor (Technical Operations)
Builds
Validated manufacturing and packaging processes for consumer health and pharmaceutical products
Domain
Pharmaceutical manufacturing / Consumer health
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
GMP validation, regulatory compliance (FDA/ICH/ANVISA), technical writing, statistics (DOE, control charts), leadership, cross-functional collaboration
Preferred skills
Pharmaceutical manufacturing process development, critical thinking, problem solving
Technologies
Manufacturing execution systems, validation software, statistical analysis tools
Responsibilities
Lead validation talent development across multiple technologies; drive validation programs aligned with business strategy; collaborate with Supply Chain, R&D, and Quality for lifecycle management; resolve complex technical challenges and lead root cause analyses; manage validation program expenses and KPIs; act as technical authority for process and equipment changes.
Seniority
Senior, hands-on IC with leadership responsibilities
