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ManpowerGroup is the leading global company for staffing solutions.
With our three brands – Manpower, Experis, and Talent Solutions – we assist companies across various industries with their recruitment needs. For 75 years, we've operated in over 75 countries, and throughout Switzerland, we support our clients in successfully completing their tasks and projects.
We are looking for a Deviation Manager BioAtrium Project - Visp
Key Responsibilities:
Take ownership of deviation records, author reports, and lead investigations from initiation to closure
Collaborate closely with subject matter experts (SMEs) and cross-functional stakeholders to determine root causes and assess potential or actual product and system impacts
Apply structured problem-solving tools such as Fault Tree Analysis, Event & Causal Factors Chart, Fishbone Diagram, or similar methodologies
Define appropriate CAPAs and effectiveness checks to address root causes and prevent recurrence
Ensure investigations are executed in full compliance with current Good Manufacturing Practices (cGMP)
Drive timely and high-quality closure of quality records within defined timelines
Support process improvement initiatives and contribute to change management activities within the operations environment
Key Requirements:
Bachelor’s degree in Chemistry, Biotechnology, Life Sciences, or a related field
Prior experience with deviation investigations and cGMP compliance in a regulated pharmaceutical or API manufacturing setting is strongly preferred
Understanding of biotech manufacturing processes and analytical testing is advantageous
Familiarity with Human and Organizational Performance (HOP) principles and risk management practices is a plus
Strong technical writing and communication skills; previous experience with investigation reports and stakeholder presentations is a clear advantage
Structured, independent working style with a high level of ownership and attention to detail
Open-minded, proactive, and adaptable to dynamic project environments
Ability to lead cross-functional teams without formal authority and manage investigations independently
Fluency in English (written and spoken); German is a plus but not required
What to Expect:
This role offers the opportunity to work in a highly regulated, quality-driven environment where your contributions directly support the production of advanced biologics. You will play a key role in maintaining product integrity and regulatory compliance, while being part of a collaborative team focused on continuous improvement and operational excellence.