INT-120456 25.06.2026

Global Project Manager

Bâle-Ville
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Pharmaceutique / Biotechnologies / Chimie
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Fixe - Temps plein

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: 24.08.2026

Latest Possible Start Date: 01.11.2026

Planned Duration of Employment: 12 months

Extension: with approved budget, project extension

Workplace: Basel

Workload: 100%

Home Office: No

Travel: Yes: Within Switzerland, Willingness to travel approximately 10-20%.

Description de la mission

In collaboration with the Technical Development Team Lead (TDTL) & Device Team Leader (DTL), the PM will translate device strategy into actionable plans, focusing on three key areas:

Planning: Define “inspection ready” Design & Development Plans
Execution: Drive team activities to meet project and design control deliverables
Team Dynamics: Ensure effective communication and facilitate team performance in a regulated environment using various processes and tools for planning, communication, budget, schedule, compliance, and risk management

Project Management 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

Profil attendu pour l'emploi

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.