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Ingenieur*in für Integration und Standardisierung MedTech - Job Opportunity at ICM Personal AG

Bassersdorf, Switzerland
Contract
Mid-level
Posted: July 23, 2025
On-site
CHF 60+ per hour

Benefits

Temporary position with potential for permanent employment offering career stability and long-term growth opportunities
Competitive hourly compensation structure providing financial flexibility and potential for higher earnings than fixed salary positions
Opportunity to work across multiple departments fostering comprehensive industry knowledge and professional network expansion

Key Responsibilities

Drive cross-functional collaboration with Production, Process Technology, R&D, and Product Engineering departments to optimize manufacturing processes and implement proactive failure prevention strategies that directly impact product quality and operational efficiency
Lead enterprise-wide production flow standardization initiatives by analyzing, understanding, and streamlining complex manufacturing processes to achieve operational excellence and scalability
Execute comprehensive process analysis and improvement projects that enhance manufacturing efficiency, reduce waste, and optimize resource utilization across the entire production landscape
Serve as a key decision-maker in the Process Change Review Board (PCRB) for standardization, directly influencing manufacturing standards and quality protocols that affect company-wide operations
Develop and implement registration concepts across the manufacturing landscape, ensuring traceability, compliance, and process documentation that supports regulatory requirements and quality assurance
Lead knowledge transfer initiatives by training new employees on internal software systems, ensuring consistent implementation of standardized processes and maintaining operational continuity

Requirements

Education

Hochschulabschluss als Ingenieure der Fachrichtung Maschinenbau, Elektrotechnik oder Hochschulabschluss in Informatik

Experience

2+ Jahre Berufserfahrung in vergleichbarer Funktion, vorzugsweise in technologischem Umfeld

Required Skills

SAP Kenntnisse und gute MS Office Kenntnisse (Word, Excel, PowerPoint) SPC Kenntnisse und Erfahrung in deren Anwendung, oder statistische Kenntnisse Exakte und detailorientierte Arbeitsweise sowie gute Kommunikations- und Präsentationsfähigkeiten Kenntnisse der Herstellung von Leiterplatten oder ähnlichen Produkten erwünscht Fliessend Deutsch, Englischkenntnisse erwünscht
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Sauge AI Market Intelligence

Industry Trends

The MedTech industry is experiencing unprecedented growth driven by aging populations, increased healthcare digitization, and post-pandemic healthcare infrastructure investments, creating strong demand for integration and standardization specialists who can optimize manufacturing processes and ensure regulatory compliance in increasingly complex production environments. Manufacturing 4.0 and Industry 4.0 initiatives are transforming medical technology production, with companies investing heavily in process standardization, digital integration, and statistical process control to meet stringent quality requirements while maintaining competitive cost structures in global markets. Regulatory pressures in medical device manufacturing continue to intensify with evolving FDA, CE marking, and ISO standards, making process standardization and integration expertise critical for companies seeking to maintain market access and competitive positioning.

Salary Evaluation

The CHF 60+ hourly rate translates to approximately CHF 100,000-125,000 annually for full-time equivalent work, which is competitive for mid-level engineering roles in the Swiss MedTech sector, particularly considering the specialized nature of process integration and standardization expertise required.

Role Significance

Typically operates within a team of 5-8 process engineers and quality specialists, while interfacing with larger cross-functional teams of 15-25 professionals across R&D, production, and quality assurance departments in medium to large-scale MedTech manufacturing operations.
This is a mid-level specialist position with significant cross-functional influence, requiring the ability to work independently while collaborating with senior leadership across multiple departments, indicating a role that bridges tactical execution with strategic process improvement initiatives.

Key Projects

Implementation of enterprise-wide process standardization initiatives that harmonize manufacturing procedures across multiple product lines and production facilities Development and deployment of integrated quality management systems that connect process control, statistical analysis, and regulatory compliance requirements Leading digital transformation projects that integrate legacy manufacturing systems with modern ERP and quality management platforms

Success Factors

Deep understanding of medical device manufacturing regulations and quality standards, combined with the ability to translate complex regulatory requirements into practical, implementable process improvements that maintain compliance while optimizing efficiency. Strong systems thinking and process optimization capabilities that enable identification of bottlenecks, inefficiencies, and improvement opportunities across complex, interconnected manufacturing processes. Exceptional communication and stakeholder management skills necessary to build consensus among diverse technical teams and drive adoption of standardized processes across traditionally siloed departments. Advanced analytical and statistical process control expertise that enables data-driven decision making and continuous improvement in high-stakes manufacturing environments where quality failures can have significant safety and regulatory consequences.

Market Demand

High demand driven by the Swiss MedTech industry's position as a global leader in medical device manufacturing, with companies increasingly requiring specialists who can bridge the gap between traditional manufacturing processes and modern digital integration requirements.

Important Skills

Critical Skills

SAP knowledge is essential as it represents the backbone of modern manufacturing resource planning and quality management systems, enabling integration of process data, inventory management, and production scheduling across complex manufacturing operations. Statistical Process Control (SPC) expertise is fundamental for maintaining the quality standards required in medical device manufacturing, where statistical validation of process capability and ongoing monitoring are regulatory requirements and competitive necessities. Cross-functional communication skills are vital for success in this role, as process standardization requires building consensus and driving change across traditionally independent departments with different priorities and perspectives.

Beneficial Skills

PCB manufacturing knowledge provides valuable context for understanding precision manufacturing processes, quality control challenges, and the integration requirements common in medical device and electronic component production. English language proficiency enhances career mobility and effectiveness in Switzerland's international business environment, particularly important for companies with global operations and regulatory requirements. Advanced Excel and PowerPoint skills support the analytical and presentation requirements necessary for driving process improvements and communicating complex technical concepts to diverse stakeholders.

Unique Aspects

The role combines traditional manufacturing engineering with modern digital integration challenges, requiring expertise in both established manufacturing processes and emerging Industry 4.0 technologies.
Positioned at the intersection of multiple critical functions including R&D, production, and quality assurance, offering exceptional visibility into end-to-end product development and manufacturing processes.
Opportunity to directly influence manufacturing standards through PCRB membership, providing decision-making authority that extends beyond typical mid-level engineering roles.
Focus on MedTech industry provides exposure to cutting-edge manufacturing technologies and stringent quality requirements that develop highly transferable and valuable expertise.

Career Growth

Progression to senior roles typically occurs within 3-5 years with demonstrated success in process standardization and cross-functional leadership, particularly in the fast-growing Swiss MedTech sector where experienced professionals are highly valued.

Potential Next Roles

Senior Process Engineering Manager overseeing multiple process improvement teams and driving strategic manufacturing excellence initiatives Quality Assurance Director responsible for enterprise-wide quality systems and regulatory compliance across international manufacturing operations Manufacturing Operations Manager leading comprehensive production optimization and digital transformation initiatives

Company Overview

ICM Personal AG

ICM Personal AG operates as a specialized staffing and recruitment firm focusing on technical and engineering positions in the Swiss market, with particular strength in placing qualified professionals in manufacturing, technology, and industrial sectors where precision and expertise are paramount.

Established player in the Swiss technical recruitment market with a reputation for matching skilled engineering professionals with leading industrial and technology companies, particularly in the German-speaking regions where technical manufacturing expertise is highly valued.
Strong presence in the Zurich metropolitan area and broader German-speaking Switzerland, serving as a bridge between international companies seeking specialized technical talent and qualified engineering professionals seeking career advancement opportunities.
Professional, results-oriented environment that emphasizes matching candidate expertise with client needs, fostering long-term career relationships rather than transactional placements, with focus on supporting both temporary and permanent career transitions.
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