CareerPlan

QMS Process Engineer

South San Francisco, USFull-time$111k–$206k2026-10-19 → 2026-11-10

Core

Design, implement, and optimize data-driven quality workflows and maintain a robust Quality Management System (QMS) for Critical-to-Quality ecosystems.

Role type

QMS Process Engineer

Builds

Operational excellence in pharmaceutical development processes

Domain

Pharmaceutical / Life Sciences / Quality Management

Required skills

Process engineering frameworks (Lean, Agile), Data analytics, Regulatory compliance (GxP, Pharmacovigilance, IVD), Trend analysis, Stakeholder collaboration

Preferred skills

AI and automation tools integration, Digital enablement, Quality data storytelling

Technologies

Lean, Agile, GxP, Pharmacovigilance, IVD

Responsibilities

Partner across teams to design and optimize quality workflows; Integrate digital enablement and automation tools; Translate raw quality data into structured insights; Maintain alignment with global regulatory standards; Support inspection readiness and regulatory intelligence analysis; Engage with stakeholders to guide compliant process updates.

Seniority

Mid-level, hands-on IC