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Industrialization Engineer

Spineart · Plan les Ouates, 1228, Switzerland · Active · BambooHR

Job facts

FieldValue
CompanySpineart
TitleIndustrialization Engineer
Normalized title-
Department / teamIndustrialization & Methods
LocationPlan les Ouates
Work model-
Employment typePermanent 100%
Salary-
Statusactive
ATS providerBambooHR
Posted / first seen2026-04-30 / 2026-05-30
Changed / last seen2026-05-30 / 2026-06-06

Related slices

PageWhat it containsOpen
Company jobsActive postings from Spineart.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through BambooHR.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Plan les Ouates.Open
Department jobsActive postings in Industrialization & Methods.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanySpineart
Source772463ed-9d98-4971-bc0c-4b6045c114f9
ATS providerBambooHR

Description

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.

Full job record

Job ID79ff6fdf4a980c731b6534ee23ad1ee5f0dec19d
Org ID532ea86e-d318-400a-9819-1dffe9336719
Source ID772463ed-9d98-4971-bc0c-4b6045c114f9
Board ID772463ed-9d98-4971-bc0c-4b6045c114f9
Providerbamboohr
Provider Job Key107
TitleIndustrialization Engineer
Normalized Title
Statusactive
Activeyes
Location TextPlan les Ouates, 1228, Switzerland
DepartmentIndustrialization & Methods
Team
Employment TypePermanent 100%
Workplace Type
Remote Policy
Country
Region
CityPlan les Ouates
Salary Raw
Salary Min
Salary Max
Salary Currency
Salary Period
Source URLhttps://spineart.bamboohr.com/careers/107
Apply URLhttps://spineart.bamboohr.com/careers/107
First Seen At2026-05-30 05:54:39Z
Last Seen At2026-06-06 10:25:27Z
Last Checked At2026-06-06 10:25:27Z
Last Changed At2026-05-30 05:54:39Z
Inactive At
Source Posted At2026-04-30 00:00:00Z
Source Updated At
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=bamboohr/board=spineart/date=2026-06-06/2026-06-06T10-25-25-301Z-d1c79651282c65b11148b50ef46625834086ed36f42d6d772699438571fcac93.json
Event Fields
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Parsed Structured
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Extensions
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Native Structured
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    "description": "<p><br><span style=\"font-size: 12pt\">Are you an experienced Industrial Engineer ready to lead industrialization projects and drive successful product transfers into manufacturing?</span><br><span style=\"font-size: 12pt\">Are you eager to join a fast‑growing organization where innovation and resilience are key drivers of success?</span></p>\n<p><br></p>\n<p>                                    If so, join our Industrialization Department as <span style=\"font-size: 12pt; font-weight: bold\">Industrialization Engineer</span><br><span style=\"font-size: 12pt\">                      You will become part of a small, dynamic team that fosters a collaborative, </span><span style=\"font-size: 12pt\">supportive, and </span></p>\n<p><span style=\"font-size: 12pt\">                                                                        passionate work environment</span></p>\n<p><br></p>\n<p><span style=\"text-decoration: underline\"><br></span></p>\n<p><span style=\"text-decoration: underline\"><span style=\"font-weight: bold\">Your mission:</span></span></p>\n<p><span style=\"text-decoration: underline\"><br></span></p>\n<p><span style=\"font-size: 12pt\">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.</span></p>\n<p><br><br></p>\n<p><span style=\"font-size: 12pt\">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,</span></p>\n<p><br><br></p>\n<p><span style=\"font-size: 12pt\">Working in close collaboration with internal stakeholders (R&amp;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.</span></p>\n<p><br><br></p>\n<p><span style=\"font-size: 12pt\">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.</span></p>\n<p> </p>\n<p><br></p>\n<p><span style=\"text-decoration: underline\"><span style=\"font-weight: bold\">Your main activities:</span></span></p>\n<p><br></p>\n<p><span style=\"font-weight: bold\">A. Manage NPI (New Product Introduction) and industrialization phases with concurrent engineering</span></p>\n<ul>\n<li>Ensure a smooth transition between R&amp;D and Manufacturing facilities either in house or with a contract manufacturing company by managing the Design Transfer activities and associated planning.</li>\n<li>Manage and coordinate the industrialization process for implants and instruments during the whole product life cycle (prototypes, test batches, expert phases and launches)</li>\n<li>Work closely with cross-functional teams, including R&amp;D, quality assurance, and production, to coordinate and troubleshoot manufacturing processes.</li>\n<li>Assist in transitioning from prototype development to full-scale production during product scaling phase.</li>\n<li>Participate in design to cost activities prior to industrialization.</li>\n<li>Evaluate and estimate in relation with the marketing and purchasing teams during the new product development the COGS to secure new business cases.</li>\n<li>Develop and secure the inspection methods for all new products such as specific inspection means &amp; gauges</li>\n</ul>\n<p><br></p>\n<p><span style=\"font-weight: bold\">B. Process management &amp; improvement</span></p>\n<ul>\n<li> <span style=\"font-size: 12pt\">Ensure a technical support during design changes and/or manufacturing changes</span></li>\n<li>Evaluate/Choose appropriate machinery and equipment for manufacturing in close relation with production team and oversee their maintenance.</li>\n<li>Analyze manufacturing costs and find ways to reduce expenses (in house and outsourced) in close relation to R&amp;D team during development and industrialization phases.</li>\n<li>Update manufacturing process documentations according to changes and improvements.</li>\n<li>Ensure that manufacturing processes adhere to industry-specific regulations and standards, such as ISO 13485 and FDA requirements.</li>\n<li>Assess and mitigate risks associated with manufacturing processes to ensure product safety.</li>\n</ul>\n<p><br></p>\n<p><br></p>\n<p><span style=\"color: rgb(0, 0, 0); font-weight: bold\"><span style=\"text-decoration: underline\">Your profile</span>:</span></p>\n<p><br></p>\n<ul>\n<li>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.</li>\n<li>Strong technical background and strong ability on product design, manufacturing processes, product inspection aiming to incorporate DFM principles.</li>\n<li>Knowledge of manufacturing processes such as CNC machining, 3D printing, and finishing processes.</li>\n<li>Strong technical ability in creating engineering drawings, models, applying GD&amp;T.</li>\n<li>Ability to use CAD software (SolidWorks preferred).</li>\n<li>Solid understanding of data flows and interfaces between PLM, ERP, QMS, and manufacturing systems.</li>\n<li>Ability to structure, maintain, and leverage products and processes data across the full product lifecycle.</li>\n<li>Good understanding of the safety requirement of the medical device (knowledge of the ISO-13485 and FDA requirements).</li>\n<li>Effective interpersonal, communication, proactive and organizational skills.</li>\n<li>Languages:  French mandatory,  Fluency in written and spoken English</li>\n</ul>\n<p><br></p>\n<p><br></p>\n<p><span style=\"font-size: 12pt\">If this role matches your profile and expectations, we would be pleased to receive your application.</span></p>\n<p><br></p>",
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