Technical Project Leader Equipment Qualification & Validation; GMP; f/m/d
Job in
4303, Kaiseraugst, Kanton Aargau, Switzerland
Listing for:
Myjob
Full Time, Seasonal/Temporary
position
Listed on 2026-07-29
Job specializations:
-
Quality Assurance - QA/QC
Regulatory Compliance Specialist, Quality Engineering
-
Pharmaceutical
Regulatory Compliance Specialist, Pharmaceutical Manufacturing, Pharma Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 110000 - 140000 CHF Yearly
CHF
110000.00
140000.00
YEAR
Job Description & How to Apply Below
Position: Technical Project Leader Equipment Qualification & Validation (GMP) (f/m/d)
Location: KaiseraugstTechnical Project Leader Equipment Qualification & Validation (GMP) (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 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.
Your tasks
Plan, coordinate, and track equipment onboarding projects from initiation to completionOrganize, prepare, and facilitate project meetings, including kick-off meetings and progress reviewsDraft and maintain User Requirement Specifications (URS) in collaboration with subject matter expertsCoordinate GMP documentation activities, including qualification, validation, and risk management deliverablesCoordinate activities across multiple stakeholders and ensure alignment with project timelines and requirementsMonitor project milestones and documentation statusContribute to the continuous improvement of equipment lifecycle management processes and standardsOur 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 environmentExperience with GMP documentation and quality systemsStrong organizational and project coordination skillsStructured, proactive, and detail‑oriented working styleExcellent communication and stakeholder management skillsAbility to work independently while collaborating effectively within cross‑functional teamsFluent in English;
German language skills are considered an advantageWhat we offer
Fair and market‑competitive compensationOpportunity for a permanent position, depending on mutual fit and business developmentState‑of‑the‑art infrastructure at a modern work locationExcellent staff restaurant offering high quality meals at fair pricesFlat 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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