20 beste Stellen als validation engineer in genève ge – aktuell auf Personalsuche

Qualification & Validation Engineer
AliveDx —Eysins, VD
- 100%
- Englisch
- Master
- Analysefähigkeit
2 Tage
Process Validation Engineer (Additive Manufacturing)
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- 100%
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CERN —Genf, GE
- 100%
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Computational Physicist (BE-OP-PS-2026-139-GRAE)
CERN —Genf, GE
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- 100%
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- Laborerfahrung
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Lead Expert Global MSAT Drug Substance (all genders)
Merck KGaA —Eysins, VD
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Qualification & Validation Engineer

AliveDx -
Eysins, VD

Jetzt bewerben

Details zur Stelle

Temporär | 100%
vor 2 Tagen

Qualifikationen

Französisch
Englisch
Master
Analysefähigkeit
Bachelor
Qualitätssysteme

Vollständige Stellenbeschreibung

At AliveDx, we empower diagnostic insights, transform patient care, and innovate for life. With over 30-years in in-vitro diagnostics, we put the health of patients first by creating innovative solutions designed for faster diagnostic results. Alba–– our blood bank reagents portfolio–– and MosaiQ®–– one of the first multiplexing and multimodality automated testing platforms––are designed to make labs more efficient and clinical decision-making more effective. Our journey started as Alba Bioscience, and later, Quotient. Today, as AliveDx, we innovate for life.

QUALIFICATION & VALIDATION ENGINEER – TEMPORARY UNTIL END 2026

AliveDx is recruiting for a Qualification & Validation Engineer to join our Engineering team – a key function ensuring that systems, equipment, and processes are compliant, reliable, and fit for purpose across the product lifecycle. The role is a full-time temporary position until end of 2026 based in Eysins, Switzerland.

YOUR MISSION

As a Qualification & Validation Engineer, you will be responsible for defining, coordinating, executing, and documenting qualification and validation activities related to equipment, utilities, facilities, computerized systems, and manufacturing processes.

You will ensure compliance with GMP, FDA, ISO, and internal quality requirements while supporting operational excellence and maintaining systems and processes in a validated and inspection-ready state throughout their lifecycle.

You will :

Develop, validate, and implement analytical methods supporting product development, manufacturing, and release.
Define and execute qualification and validation strategies for equipment, systems, utilities, and manufacturing processes
Coordinate and perform qualification and validation activities including IQ/OQ/PQ, process validation, and requalification activities
Draft and maintain validation documentation including URS, risk assessments, protocols, reports, SOPs, and technical procedures
Ensure validation activities and documentation comply with GMP, GDP, FDA, ISO, and internal quality standards
Collaborate closely with Engineering, Manufacturing, QA, and QC teams to support implementation of new equipment and process improvements
Support deviation investigations, root cause analysis, CAPA, and change control activities impacting validated systems
Participate in audits, inspections, and continuous improvement initiatives to maintain operational and regulatory compliance

This role requires strong technical expertise, attention to detail, and the ability to work cross-functionally in a regulated environment to ensure product quality, patient safety, and compliance.

YOUR COMPETENCIES

Bachelor or Master degree in Engineering, Life Sciences, or related field
Minimum 2–5 years of experience in qualification/validation within a regulated industry (medical devices, pharma, biotech)
Strong knowledge of GMP, GDP, FDA, and ISO requirements and quality systems
Experience in drafting and reviewing technical and GMP documentation
Good understanding of qualification and validation lifecycle methodologies and risk-based approaches
Experience with deviation investigations, CAPA, and Change Control processes
Strong analytical, organizational, and problem-solving skills with the ability to manage multiple priorities
Fluent in French and English (written and spoken)

WHAT WE OFFER

A highly dynamic and growing environment,
An opportunity to live your passion for an intrapreneurial mindset, where cultivating innovation and customer centricity are at the heart of everything we do,
A flexible working environment where applicable and a range of core and flexible benefits, ranging from lunch allowance support, additional annual leave, cycle to work scheme, technology and access to marketplace discounts.

Interested? We invite you to send your application, including your resume and any other relevant documents. We look forward to exploring your potential contributions to AliveDx.

AliveDx is an equal opportunity employer and welcomes applications from all qualified individuals regardless of nationality, sex, disability, religion/belief, sexual orientation or age. All aspects of employment including the decision to hire, promote, discipline, or discharge, will be based on competences, performance and business needs.

Jetzt bewerben

Erweiterte Suche

validation engineer Jobs in genève ge

Qualification & Validation Engineer

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Lead Expert Global MSAT Drug Substance (all genders)

Software Engineer - Software Reliability (TE-MPE-CB-2026-93-GRAP)

Instrumentation Engineer (TE-CRG-IC-2026-94-GRAP)

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