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Overview
Talent Acquisition Manager - Life Science & Pharmaceuticals for Consultys - Beyond Conception - Be On Quality - AM Group - AL Engineering - SP Group…
We are looking for a CQV Thermal Mapping Consultant to join our teams in Visp and provide subject matter expertise in thermal validation activities for process and support equipment.
Responsibilities
* Act as Subject Matter Expert (SME) in thermal validation for equipment such as autoclaves, SIP systems, refrigerators, and freezers.
* Lead qualification activities, including commissioning, qualification, requalification, decommissioning, and periodic reviews.
* Execute and oversee qualification testing, collaborating with external service providers and internal stakeholders (Operations, Engineering, QA).
* Prepare, review, and approve qualification plans, protocols, and reports across CAPEX and OPEX phases, ensuring compliance with guidelines and SOPs.
* Ensure DQ documentation (URS, GMP risk assessments, uCQP) reflects operational requirements and update GMP risk analyses after OQ for PQ readiness.
* Manage documentation in paper-based or electronic systems (e.g., KNEAT), ensuring traceability and proper filing within CQ dossiers.
* Lead resolution of deviations, CAPAs, and technical changes through Trackwise, and participate in deviation review meetings.
* Provide technical input during audits from regulatory authorities, customers, and internal quality teams.
* Deliver training on cornerstone curriculum topics, perform OJTs, and maintain compliance with training requirements.
* Support continuous improvement, maintenance activities, and equipment optimization initiatives.
Your Profile
* Bachelor’s degree in Science or a technical discipline.
* Proven expertise in thermal validation processes and equipment.
* Hands-on experience with Ellab software solutions (ValSuite, eVal Pro), data loggers, and thermocouples.
* Strong technical writing skills with experience authoring validation deliverables.
* Detail-oriented with strong problem-solving and risk assessment capabilities.
* Skilled in managing change control processes and ensuring compliance.
* Excellent communication skills with ability to collaborate across teams and with service providers.
* Flexible, proactive, and adaptable to evolving project needs.
* Fluency in English is required, German is a plus.
Seniority level
Associate
Employment type
Full-time
Job function
* Quality Assurance and Manufacturing
Industries
* Business Consulting and Services
* Biotechnology Research
* Pharmaceutical Manufacturing
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