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Team Lead CQV 80-100% (m/w/d)

CH - Visp💼 Full-time🗓 2026-09-17 → 2026-09-26

Core

Lead a CQV team responsible for planning, coordinating, and executing qualification activities for pharmaceutical manufacturing equipment, systems, and processes.

Role type

Senior Team Lead, Commissioning, Qualification, and Validation (CQV)

Builds

Qualified pharmaceutical manufacturing systems and processes

Domain

Life Sciences / Pharmaceutical Manufacturing

Deliverable

production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work

Required skills

Team leadership, CQV project management, stakeholder coordination, external vendor management, audit support, GMP/GxP compliance, risk analysis, technical documentation (DQ/IQ/OQ/PQ)

Preferred skills

Coaching and team development, knowledge management, strategic competency planning

Technologies

GMP, GxP, DQ, IQ, OQ, PQ, Risk Analysis

Responsibilities

Lead and organize a CQV team; Plan and monitor qualification activities for complex equipment and systems; Manage external service providers and suppliers; Support audits and inspections; Ensure long-term availability of critical CQV competencies

Seniority

Senior, hands-on IC with leadership responsibilities

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