Quality Systems Engineer – MedTech & Life Sciences

Tech'Firm Industrie AG; Neuenburg; On-site; CHF 110,000 - 150,000; Full time

Job summary

Techfirm Engineering in Neuchâtel, Switzerland, seeks a Quality System Engineer to lead the deployment, compliance, and continuous improvement of the QMS in a regulated medical/technical environment.

You will support audit readiness, CAPA, root‑cause analysis, records management, regulatory documentation, and involvement in new product development.

Fluent in French and English, with a Bachelor’s or Master’s in a related field and 3+ years’ experience; on‑site role at 2000 Neuchâtel, immediately.

Qualifications

• Experience in a medical/regulated environment.
• Record management and quality documentation exposure.
• Experience supporting internal and external audits.
• Knowledge of CAPA, root cause, corrective actions, and investigations.
• Strong documentation, organizational and analytical skills.

Responsibilities

• Lead deployment and application of Quality Systems across the organization.
• Conduct periodic checks to verify quality processes.
• Act as Records Coordinator for archives and documentation.
• Support audit readiness and participate in internal/external audits.
• Investigate, respond to, and remediate audit observations.
• Identify quality issues root causes and implement corrective actions.
• Follow up on CAPA and corrective action plans.
• Lead or participate in quality improvement initiatives.
• Use quality tools and data-driven reports to improve processes.
• Communicate quality issues to stakeholders and management.
• Support compliance with Health, Safety & Environment requirements.

Skills

Quality Systems

CAPA

Root cause analysis

Audit readiness

Documentation

Data analysis

Communication

Cross-functional teamwork

Education

Bachelor's or Master’s degree in Quality/Engineering/Life Sciences/MedTech

Tools

Microsoft Office

Job description

Techfirm Engineering in Neuchâtel, Switzerland, seeks a Quality System Engineer to lead the deployment, compliance, and continuous improvement of the QMS in a regulated medical/technical environment.

You will support audit readiness, CAPA, root‑cause analysis, records management, regulatory documentation, and involvement in new product development.

Fluent in French and English, with a Bachelor’s or Master’s in a related field and 3+ years’ experience; on‑site role at 2000 Neuchâtel, immediately.