20 beste Stellen als assurance engineer – aktuell auf Personalsuche

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Industrialization Engineer

Spineart -
Plan-les-Ouates, GE

Direkt bewerben

Details zur Stelle

Festanstellung | 100%
vor 3 Tagen

Qualifikationen

Französisch
Englisch
SolidWorks
Produktion
Kommunikationsfähigkeit

Vollständige Stellenbeschreibung

Are you an experienced Industrial Engineer ready to lead industrialization projects and drive successful product transfers into manufacturing?
Are you eager to join a fast‑growing organization where innovation and resilience are key drivers of success?

If so, join our Industrialization Department as Industrialization Engineer
You will become part of a small, dynamic team that fosters a collaborative, supportive, and

passionate work environment

Your mission:

You will lead and oversee industrialization phases to ensure the efficient, robust, and successful transfer of new products into manufacturing, including the coordination of production ramp‑up activities.

You will contribute to the definition and deployment and continuous improvement of manufacturing processes, with a strong focus on productivity, industrial robustness and cost efficiency,

Working in close collaboration with internal stakeholders (R&D, Operations, and Quality), as well as internal manufacturing sites, contract manufacturing organizations (CMOs), and suppliers, you will coordinate industrial transfer activities and ensure alignment of product and manufacturing data.

You will also train and support internal teams as needed (products, processes, and tools) and act as a cross‑functional interface for PLM and industrial IT systems, including ERP and QMS where applicable.

Your main activities:

A. Manage NPI (New Product Introduction) and industrialization phases with concurrent engineering

Ensure a smooth transition between R&D and Manufacturing facilities either in house or with a contract manufacturing company by managing the Design Transfer activities and associated planning.
Manage and coordinate the industrialization process for implants and instruments during the whole product life cycle (prototypes, test batches, expert phases and launches)
Work closely with cross-functional teams, including R&D, quality assurance, and production, to coordinate and troubleshoot manufacturing processes.
Assist in transitioning from prototype development to full-scale production during product scaling phase.
Participate in design to cost activities prior to industrialization.
Evaluate and estimate in relation with the marketing and purchasing teams during the new product development the COGS to secure new business cases.
Develop and secure the inspection methods for all new products such as specific inspection means & gauges

B. Process management & improvement

Ensure a technical support during design changes and/or manufacturing changes
Evaluate/Choose appropriate machinery and equipment for manufacturing in close relation with production team and oversee their maintenance.
Analyze manufacturing costs and find ways to reduce expenses (in house and outsourced) in close relation to R&D team during development and industrialization phases.
Update manufacturing process documentations according to changes and improvements.
Ensure that manufacturing processes adhere to industry-specific regulations and standards, such as ISO 13485 and FDA requirements.
Assess and mitigate risks associated with manufacturing processes to ensure product safety.

Your profile:

Engineer degree in engineering mechanic or industrial (INSA, UTC, Polytech or equivalent) with at least 5 years of experience in similar position (manufacturing engineer or project manager) within Medtech companies.
Strong technical background and strong ability on product design, manufacturing processes, product inspection aiming to incorporate DFM principles.
Knowledge of manufacturing processes such as CNC machining, 3D printing, and finishing processes.
Strong technical ability in creating engineering drawings, models, applying GD&T.
Ability to use CAD software (SolidWorks preferred).
Solid understanding of data flows and interfaces between PLM, ERP, QMS, and manufacturing systems.
Ability to structure, maintain, and leverage products and processes data across the full product lifecycle.
Good understanding of the safety requirement of the medical device (knowledge of the ISO-13485 and FDA requirements).
Effective interpersonal, communication, proactive and organizational skills.
Languages: French mandatory, Fluency in written and spoken English

If this role matches your profile and expectations, we would be pleased to receive your application.

Direkt bewerben

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