Technical Project Leader Equipment Qualification & Validation (GMP) (f/m/d) Work location: 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 high‑quality products to market faster.
At Solvias, we serve the world’s 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.
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 Bachelor’s/Master’s 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 market‑competitive compensation
Opportunity for a permanent position, depending on mutual fit and business development
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.
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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 high‑quality products to market faster.
At Solvias, we serve the world’s 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.
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 Bachelor’s/Master’s 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 market‑competitive compensation
Opportunity for a permanent position, depending on mutual fit and business development
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.
#J-18808-Ljbffr
Technical Project Leader Equipment Qualification & Validation (GMP) Arbeitgeber: Solvias
Solvias ist ein hervorragender Arbeitgeber, der seinen Mitarbeitern die Möglichkeit bietet, in einem dynamischen und innovativen Umfeld zu arbeiten. Mit einem starken Fokus auf Mitarbeiterentwicklung und einer offenen Unternehmenskultur fördern wir Teamarbeit und individuelle Entfaltung. Unsere zentrale Lage in der Nähe von Basel, Schweiz, ermöglicht es Ihnen, Teil eines globalen Netzwerks zu sein und an bedeutenden Projekten in der Pharma- und Biotech-Branche mitzuwirken.
