Technical Project Leader Metrology (f/m/d)

Work locaction: Kaiseraugst Workload: 100% Contract time: temporary Long-term temporary employment with the option of a permanent position

Who we are

Solvias is an internationally recognized provider of integrated solutions for contract research. With its headquarters in Kaiseraugst near Basel more than 500 highly qualified employees are proud to place science at the heart of customer service helping to bring safe and highquality products to market faster.

At Solvias we serve the worlds leading pharmaceutical innovators. That offers you the opportunity to make a meaningful impact on the health of patients worldwide working with brilliant scientists in a fast-moving environment filled with stimulating challenges.

Description of your role

To strengthen our Metrology team we are looking for a Technical Project Leader to support the onboarding of laboratory equipment in a GMP-regulated environment.

In this role you will be responsible for coordinating equipment onboarding projects and ensuring the timely preparation of GMP-compliant documentation. You will collaborate closely with subject matter experts equipment users engineering teams quality representatives and external vendors.

Your tasks

• Plan coordinate and track equipment onboarding projects from initiation to completion
• Organize prepare and facilitate project meetings including kick-off meetings and progress reviews
• Draft and maintain User Requirement Specifications (URS) in collaboration with subject matter experts
• Coordinate GMP documentation activities including qualification validation and risk management deliverables
• Coordinate activities across multiple stakeholders and ensure alignment with project timelines and requirements
• Monitor project milestones and documentation status
• Contribute to the continuous improvement of equipment lifecycle management processes and standards

Our requirements

• Education as a Laboratory Technician or equivalent qualification or a Bachelors/Masters degree in a scientific discipline (e.g. Life Sciences Chemistry Pharmaceutical Sciences Biology)
• Experience working in a GMP-regulated pharmaceutical environment
• Experience with GMP documentation and quality systems
• Strong organizational and project coordination skills
• Structured proactive and detail-oriented working style
• Excellent communication and stakeholder management skills
• Ability to work independently while collaborating effectively within cross-functional teams
• Fluent in English; German language skills are considered an advantage

What we offer

• Fair and marketcompetitive compensation
• Opportunity for a permanent position depending on mutual fit and business development
• Stateoftheart infrastructure at a modern work location
• Excellent staff restaurant offering high quality meals at fair prices
• Flat hierarchies and a collaborative and international working environment

*Please note that as part of this recruitment process we cooperate with an external provider.