cross-ING AG
Yverdon-les-Bains
2 days ago
Validation Engineer
- 24 April 2026
- 100%
- Permanent position
- Yverdon-les-Bains
Job summary
cross-ING is an independent Swiss engineering company certified ISO 9001/13485. Join a dynamic team focused on product development and value creation.
Tasks
- Plan and document software and process validations like MES and SCADA.
- Conduct qualifications (DQ/IQ/OQ/PQ) and provide GMP guidance.
- Facilitate risk analyses and act as a liaison between production and quality.
Skills
- Degree in engineering, computer science, or life sciences; 3+ years in validation.
- Strong knowledge of GMP, GAMP, and ISO standards.
- Fluent in German and French (C1) plus good English (B2).
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About the job
cross-ING is an independent ISO 9001/13485-certified Swiss engineering company. The company offers customers a broad range of knowledge in the field of product development. cross-ING supports customers with many years of experience and globally networked, interdisciplinary expertise to create new things and generate added value. The cross-ING Group AG also takes on administrative tasks in the areas of marketing, sales, and human resources.
Pharmaceutical and medical companies in the canton of Vaud regularly face the challenge of validating their products and systems according to applicable regulations. To support these companies, we are immediately looking for the location in Yverdon-les-Bains a Validation Engineer who performs qualification and validation tasks according to current standards and guidelines
Your Responsibilities
Planning, execution, and documentation of software and process validations, e.g., MES, SCADA, automation systems, and production processes
Planning, execution, and documentation of qualifications (DQ/IQ/OQ/PQ)
Consulting companies on GMP, GAMP, CAPA topics
Moderation and execution of risk analyses (e.g., GMP-RA, FMEA)
Interface function between production and quality management at the customer
Your Qualifications
University degree in engineering, computer science, life sciences, or comparable education
At least 3 years of professional experience in qualification and/or validation in a regulated environment (pharmaceutical or medical preferred)
Solid knowledge of GMP, GAMP, 21 CFR Part 11, ISO 13485, ISO 9001, and data integrity
Technical understanding and analytical thinking skills
Experience in technical writing is an advantage
Good ERP knowledge (application and implementation) is an advantage
Structured, team-oriented, and interculturally open working style
Very good German and French skills (each level C1) as well as good English skills (level B2) in spoken and written form
What We Offer
As soon as a suitable start project is available, we offer you a varied and responsible position in a permanent employment with us. We ensure that you always receive challenging projects that match your profile and that you can learn a lot to enhance your current skills. Our employment conditions offer modern frameworks with attractive benefits.
Our Benefits at a Glance:
🚀 Internal specialist courses & campus formats – for your targeted knowledge boost
🎓 Support for external training – if it fits professionally, we support you
🤝 Referral bonus – employees recruiting employees pays off
💼 Sales incentive – successful project placement pays off
🕒 Flexible time off – buy additional vacation or take unpaid leave
🛡️ Modern pension solution (Swiss Life / ASGA) – solidly secured for the future
💸 Discounts & partner offers – benefits at banks, mobility & shopping
Interested?
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