Commissioning and Qualification Lead
Vor 6 Tagen
Join a global life sciences company driving innovation in pharmaceutical manufacturing. We're seeking a C&Q Lead to oversee commissioning and qualification of new equipment, facilities, and processes at our Visp site.
Key Responsibilities:
- Lead and mentor engineers and technicians on C&Q activities.
- Develop and execute GMP-compliant qualification and validation strategies.
- Manage IQ/OQ/PQ documentation and ensure regulatory compliance.
- Collaborate with engineering, manufacturing, quality, and regulatory teams.
- Oversee project scope, cost, and timelines for CAPEX initiatives.
- Serve as C&Q subject matter expert and implement best practices.
Requirements:
- Degree in Engineering, Science, or related field (Master's preferred).
- Experience in commissioning, qualification, and validation in GMP pharma/biotech.
- Strong leadership and project management skills in CAPEX or facility projects.
- Fluent in English; German a plus.
- Analytical, commercially aware, and capable of leading teams to project success.
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