Flexsis
Global Project Manager
Skills
2 months ago
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Important information
Contract type:
Freelance / Contract
Location:
Basel, Switzerland
Work mode:
Onsite
Published on:
7 August 2026
What they need
Flexsis is a company of the Interiman Group, one of the leading providers of personnel services in Switzerland. Thanks to our solid expertise as well as the competencies within the Interiman Group, we offer tailored solutions in personnel consulting.
For our client Roche in Basel , we are looking for a reliable and motivated (m/f/d).
Global Project Manager
- Start Date: 01.09.2026
- Latest Possible Start Date: 01.11.2026
- Planned Duration of Employment: 12 months
- Extension: with approved budget, project extension
- Workplace: Basel
- Workload: 100%
Tasks & Responsibilities:
- Maintains full understanding of program milestones for the Core, Lifecycle, Technical Development and associated teams and links them to the Device Team plan
- Effectively applies PM best practices and utilizes tools for planning, communication, team building, collaboration, decision-making, issue & risk management, lessons learned, knowledge management and budget tracking
- Develops & updates Design & Development Plan and establishes contingency plans as needed
- Identifies team risks and mitigation plans
- Manages project scope and facilitate necessary changes
- Assesses Team dynamics and leads team building activities to enable and sustain a high performing team environment
- Establish relationships and network with other stakeholder Teams and PMs
- Develops and adapts project communication tools to drive awareness of project progress and risks across stakeholders including external collaborators (e.g. dashboard)
- Acts as Device Team Leader back-up for Team communication as required
Must Haves:
- Bachelor's degree in Engineering or a related field.
- Min. 8 to 11 years of experience, with at least 5 years in a relevant industry, preferably within a global medical device, pharmaceutical, or biopharmaceutical company
- Experience in project management in drug and/or medical device development and commercialization, particularly with combination products
- Proficiency in Project Management best practices and software (Microsoft Project, Smartsheet, Google suite)
- PMP certification is an asset.
- Knowledge of 21CFR820.30 design control requirements
- Fluent English is required. German, Japanese or Danish is of advantage
Have we sparked your interest and would you like to take your chance? Then we should definitely get to know each other! Simply click on “Apply now” and we look forward to receiving your complete application documents.
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