We are seeking a highly motivated Process & Risk Management Specialist to support complex development projects in the diagnostics sector. This role is ideal for someone who thrives in structured environments and enjoys working cross-functionally to ensure quality and compliance in regulated product development.
Key Responsibilities
* Guide and optimize processes across system and assay development projects
* Manage multi-level requirements and conduct detailed risk assessments
* Maintain risk and requirements documentation in centralized databases
* Lead Configuration Management and Verification activities
* Collaborate with Development, QA, Regulatory, Medical Affairs, and external partners
* Deliver high-quality documentation and ensure inspection readiness
* Independently manage work packages and prioritize tasks effectively
Must-Have Qualifications
* University degree in Life Sciences, Natural Sciences, or Engineering
* Experience in product development within a regulated (GMP) environment
* Strong technical understanding of development processes
* Excellent analytical, organizational, and communication skills
* Fluent in English (German is a plus)
* Ability to lead by influence and drive results across teams
Preferred Qualifications
* Experience in the diagnostics industry
* Familiarity with Risk, Requirements, Configuration, or Verification Management
* Database and process management tool experience
* Strong presentation and stakeholder engagement skills
Please note:
* This is a contract position with a length of 12 months with possibility of extension
* You must have the right to work in Switzerland to be eligible for this role
* Only shortlisted candidates will be contacted.
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