Description

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ManpowerGroup is the world's leading company for workforce solutions.
With our three brands – Manpower, Experis, and Talent Solutions – we support companies from various industries with their recruitment needs. For 75 years, we have been operating in over 75 countries and accompany our clients throughout Switzerland to successfully carry out their tasks and projects.
MSAT Cleaning Validation Expert
About the Role
We are looking for an experienced MSAT Cleaning Validation Expert to support equipment cleaning validation activities within a GMP\-regulated biopharmaceutical manufacturing environment in Visp.
In this role, you will provide technical expertise, ensure compliant validation documentation, support operational readiness, and contribute to successful customer and regulatory inspections. You will work closely with MSAT, QA, QC, Manufacturing and R\&D to ensure that cleaning validation processes are robust, inspection\-ready and aligned with regulatory expectations.
Key Responsibilities
Lead and execute cleaning validation activities for manufacturing equipment and associated systems
Prepare, review and finalise validation protocols, reports and GMP\-relevant documentation
Support cleaning validation execution for systems such as COP, CIP, USP, DSP and buffer/media preparation equipment
Perform and support parts washer COP validation activities
Manage the SOP lifecycle for cleaning validation topics, including authoring, review, updates and approval coordination
Collaborate with R\&D, Manufacturing, QC and QA on the development, optimisation and validation of new or modified cleaning processes
Ensure validated cleaning methods are implemented compliantly within routine manufacturing operations
Act as technical SME and coordinator for cross\-functional cleaning validation projects
Conduct cleaning validation impact assessments for deviations, change requests and technical change requests, including DRs, CRs and TCRs
Support customer and regulatory inspections by preparing, explaining and presenting validation data, rationale and documentation
Evaluate customer requests and inquiries related to cleaning validation topics
Ensure consistency and appropriate oversight of cleaning validation activities across BioAtrium
Required Profile
Degree in Life Sciences, Biotechnology, Chemical Engineering or a comparable scientific discipline
Proven experience in GMP cleaning validation within a pharmaceutical or biopharmaceutical manufacturing environment
Hands\-on experience with equipment cleaning validation, ideally including COP, CIP, USP, DSP and buffer/media preparation systems
Strong understanding of FDA and EMA expectations related to cleaning validation, contamination control and GMP compliance
Experience writing and reviewing validation protocols, reports and GMP SOPs
Ability to assess cleaning validation impact in the context of deviations, changes and technical requests
Experience supporting or participating in customer audits and regulatory inspections
Strong documentation skills and a structured, detail\-oriented working style
Good analytical skills and ability to interpret validation data
Strong cross\-functional collaboration skills and confidence working with MSAT, QA, QC, Manufacturing and R\&D
Ability to act as a technical subject expert in a project\-driven environment
Fluent English skills; German is an advantage
Assignment Details
Location: Visp, Switzerland
Workload: Full\-time
Work model: On\-site
Contract duration: Until 31 December 2026
Extension: Possible extension of 1 month
Environment: GMP\-regulated biopharmaceutical manufacturing site
Karrierestufe
Berufserfahren
Branche
Biotechnologieforschung
Beschäftigungsverhältnis
Vollzeit
Tätigkeitsbereiche
Qualitätssicherung
Kenntnisse und Fähigkeiten
Gute Herstellungspraxis (GMP)
Analytische Fähigkeiten
Dokumentation
Inspektion
Reinigungsvalidierung
Fertigung
Qualitätssicherung
Englisch jid0d860d4jm jit0418jm jiy26jm