Global Project Manager Combination Products; m/f/d); temporary or -lance
Job in
4040, Basel, Kanton Basel-Landschaft, Switzerland
Listed on 2026-09-14
Listing for:
Congenius AG
Seasonal/Temporary
position Listed on 2026-09-14
Job specializations:
-
Engineering
Regulatory Compliance Specialist, Operations Management -
Management
Project & Program Management, Regulatory Compliance Specialist, Operations Management
Job Description & How to Apply Below
Global Project Manager Combination Products (m/f/d) (temporary or freelance, 100%) Your Responsibilities
- Lead global product development, lifecycle management and continuous improvement projects in the medical device/pharma environment.
- Translate product strategy into executable project plans together with cross-functional leadership.
- Plan, execute and monitor projects to ensure delivery of milestones, timelines, budgets and quality objectives.
- Coordinate cross-functional teams, external vendors and global stakeholders throughout the project lifecycle.
- Develop and maintain Design & Development Plans in compliance with regulatory requirements.
- Proactively identify, assess and mitigate project risks while managing scope, resources and changes.
- Apply project management best practices for planning, communication, governance and decision-making.
- Facilitate effective team collaboration, governance reviews and stage-gate processes.
- Maintain project documentation, dashboards and knowledge management to ensure transparency and continuous improvement.
- Bachelor's or Master’s degree in Engineering or a related scientific or technical discipline.
- 8–11 years of professional experience, including at least 5 years within the medical device, pharmaceutical or biopharmaceutical industry.
- Proven experience managing drug and/or medical device development and commercialization projects, preferably involving combination products.
- Strong knowledge of project management methodologies and tools including Microsoft Project, Smartsheet and Google Suite.
- Solid understanding of 21 CFR 820.30 Design Control requirements.
- Experience working with external suppliers and strategic development partners.
- Ability to independently manage multiple complex projects in a fast-paced global environment.
- Excellent communication, stakeholder management and relationship-building skills.
- PMP certification is considered an advantage.
- Fluent English is mandatory;
German, Japanese or Danish is an advantage. - You will work in Basel for an ambitious, dynamic company with a very good working atmosphere
- You benefit from a versatile field of activity
- You work in a company with a flat hierarchy, short decision-making processes
- You can expect a pleasant working atmosphere, an uncomplicated and collegial cooperation
- You benefit from modern and attractive working conditions
- An attractive salary and very good social benefits round off the offer
- The contract is limited to 1 year with a high likelihood of an extension
Congenius provides tailored expertise and leadership to global firms, established SME`s and aspiring start-ups in the medical device, IVD and pharmaceutical industry. If you enjoy working with a diverse range of people across a broad range of projects and are passionate about making a positive contribution to the Med Tech industry, then joining our dynamic team could be your next rewarding career step.
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