Experienced Medical Device Product Development Engineer Job at Life Science Talent (Aarhus)

Director Project Leadership

The Director of 2008 Product manages and sustains the product in the U.S. market...

Location

United States of America , Concord

Salary:

Not provided

Fresenius Kidney Care Eupora

Expiration Date

Until further notice

Requirements

Masters (M.S.) Degree in a related technological field required
Doctoral (Ph.D.) Degree in a related technological field strongly preferred
Minimum 10+ years' related experience
5+ years' experience as a Manager
or 5+ years' experience in a senior managerial role
Strong and experienced manager in both direct and indirect people management
Effective negotiation and conflict resolution skills
Strong interpersonal skills
Experience successfully collaborating with internal and external stakeholders
Able to delegate activities and manage resources, as well as to multitask, prioritize, and meet deadlines

Job Responsibility

Leads the global product development group (PDG) in the Product Engineering Center (PEC)
Responsible for developing and leading product development teams
Responsible for global product design oversight for the PEC including harmonizing and sustaining global product designs
Conducts research and development towards innovative products and identifying new technology platforms
Applies in-depth understanding to lead multicultural cross-functional activities and project activities in a variety of geographic locations
Meets departmental and organizational objectives, facilitates issue resolution and performs managerial related duties
Provide strategic leadership of short- and long-term goals
In collaboration with other senior management, develop, implement, and maintain a global product development strategy
Develops detailed engineering and scientific specifications for major engineering projects
Prepares and presents to executive management project updates, design concepts, and other information as needed

What we offer

medical insurance
dental insurance
vision insurance
a 401(k) with company match
paid time off
parental leave
potential for performance-based bonuses depending on company and individual performance

Fulltime

Algorithm Engineer IV

Beacon Biosignals is on a mission to revolutionize precision medicine for the br...

Location

United States , Boston

Salary:

Not provided

Beacon Biosignals

Expiration Date

Until further notice

Requirements

More than 5 years of industry experience in machine learning and deep learning, particularly in health sciences or other regulated fields, with a proven track record of bringing algorithms into production
Experienced with digital signal processing (DSP) and statistics
Proficient in using PyTorch (preferred) or other deep learning frameworks for training, developing, and deploying deep learning models
Proficient with latest Deep Learning advances (Transformer/ViT, large scale modeling, large model training, ...)
Follow and spread best practices in software and ML engineering, including testing, version control, code reviews, documentation, Dockerization, CI/CD, and experiment tracking
Experienced with biosignals, medical imaging data, or large time-series datasets, or are enthusiastic about learning more in the domain
Thrive in a team environment, recognizing that collaboration, open communication, and continuous feedback are essential for collective success
Can distill, discuss, and present complex technical topics in a way that is appropriate for the audience at hand, both internally and externally
Excited to participate in the entire algorithm development lifecycle, which spans scoping, data wrangling, algorithm development/experimentation, formal validation, quality/regulatory documentation, production deployment, and working with clients who might benefit from these algorithms

Job Responsibility

Participate in and lead the entire biosignal-based algorithm development lifecycle for medical devices including specifications and requirements gathering, data curation and labeling, development, failure-analysis, production, maintenance, and documentation
Select, implement, and develop the most appropriate method for each problem, knowing when to apply deep learning techniques and when other methods are more effective
Enhance our internal deep learning and machine learning tools to boost team efficiency, introduce new model architectures and algorithmic techniques, and refine the codebase to encourage reusability where needed to enable rapid experimentation
Spread and improve our best practices to ensure algorithm implementations are user-friendly, well-documented, and thoroughly tested, including unit tests, comprehensive documentation, CI, and non-regression testing
Present results to key stakeholders and assist them in utilizing algorithms for client engagement
Support the client-facing projects to understand and shape the impact Beacon algorithms have for our customers, both for existing deployed algorithms, and future algorithm development

What we offer

Equity
PTO

Sr. Mechanical Engineer

We are seeking a highly motivated engineer for a unique opportunity to join a fa...

Location

United States , San Diego

Salary:

50.00 - 54.00 USD / Hour

MillenniumSoft Inc

Expiration Date

Until further notice

Requirements

BS – Mechanical Engineering, Materials Engineering or Biomedical Engineering with emphasis on mechanical design and development
Minimum 5 years of product design and development experience
Working knowledge of design control processes and creating and maintaining design control documentation
Experienced in requirements engineering, hazards analysis, FMEA, verification and validation
Excellent knowledge of fundamental Mechanical Engineering principles and strong experience in their application to solving manufacturing and engineering problems
Prior experience of leading or working as part of a cross-functional team with members from marketing, sales, clinical, regulatory, operations etc.
Strong analytical ability and demonstrated problem-solving skills
Excellent verbal and written communication skills
Ability to work independently and to direct junior engineers and technicians
Ability to manage multiple projects of varying scopes at once

Job Responsibility

Think beyond the parts and understands how the products are developed(beyond the design)
Step in at times and become the PM as needed
Value engineering and commercializing disposable infusion products
Working cross-functionally to understand end-user needs, translating those into system requirements, developing robust design solutions, and supporting design transfer to manufacturing and operations
Proactively manage technical risks, drive feasibility testing, robustness testing, manage error budgets, cost models, and drive timely completion of projects
Projects can involve automation, mechanical design, mechanical testing, materials engineering and other types of mechanical engineering projects

Fulltime

Sr Mgr, Interoperability

Join Baxter in our mission to save and sustain lives by developing high quality ...

Location

India , Whitefield, Bangalore

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

BS in relevant engineering disciplines, MS preferred
15+ years of experience
Must be experienced areas of System Engineering, particularly requirements and test/verification
Must be experienced with managing digital interfaces, interoperability, and/or connectivity of devices
Requires strong organization and communication skills, with the ability to interface with both technical and non-technical personnel
Must be able to provide solutions that reflect understanding business objectives and cost implications
Proven track record of management/leadership effectiveness

Job Responsibility

Managing Interoperability and connectivity of the organizations portfolio of products through clear definition of interface specifications and test methods that ensure cohesive and secure integration of internal and external products throughout the product lifecycles
Functional management of Systems Engineers, Verification Engineers, and Digital Interface Technical Leaders
Develop and implement a global interoperability testing strategy
Develop and retain talent for the interoperability organization locally
Drive mature interoperability to enable future digital product solutions
Direct technical subject matter experts on multiple programs who are responsible for the following: Interoperability and connectivity related user requirements
External and custom interface specifications and associated test methods
Collaboration with cross-business peers to facilitate device interoperability across the company
Product features that rely upon interoperability throughout the development process and the product lifecycle
Testing systems of systems to ensure deployment scenarios operate as intended

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Senior Embedded Software Engineer

Eitan Medical is seeking an experienced Embedded Software Engineer to help devel...

Location

Israel , Netanya

Salary:

Not provided

Eitan Medical

Expiration Date

Until further notice

Requirements

Experienced Embedded Software Engineer
hands-on engineer with deep technical expertise
enjoys tackling complex challenges
owning system components end-to-end
collaborating closely with multidisciplinary teams

Job Responsibility

Participate in the full development lifecycle from concept, architecture, and coding to integration, testing, verification, and production validation
Design and implement embedded software for safety-critical medical devices
Develop firmware, drivers, communication protocols, and RTOS-based components
Collaborate with hardware, product, QA, and cloud teams to define and refine system requirements
Support board bring-up and perform hardware–software integration and deep system debugging
Build robust diagnostics, monitoring, and logging capabilities to enhance field performance
Troubleshoot complex issues involving timing, real-time behavior, connectivity, and stability
Contribute to architecture discussions, code reviews, and continuous engineering improvements
Ensure development aligns with medical-grade quality, safety, and cybersecurity standards

Fulltime

Expert Biocompatibility

At Fresenius Medical Care, we are the global leader in kidney care, committed to...

Location

Germany , St. Wendel; Bad Homburg; Schweinfurt

Salary:

Not provided

FMS USA Fresenius Mgmt Services Inc

Expiration Date

Until further notice

Requirements

Successfully completed bachelor’s or master’s degree in scientific or engineering or a similar technical field required, such as medical technology
Related working experience: first years to 5 years, depending on level (Junior Expert / Expert)
First experience in writing biocompatibility evaluations
Knowledge with biocompatibility-testing and evaluations of medical devices according to ISO 10993
Application of Design Control and Risk Management and knowledge and familiarity with the concepts of FDA CFR 820, ISO 13485, and ISO 14971
Knowledge with medical device risk management process and related regulations
Experience with product or design and development or quality engineering of sterile disposables utilizing various plastic processes such as injection molding and extruding
Ability to communicate technical information to non-technical audiences
Familiar with agile methodology
First Experience with ALM and PDM systems

Job Responsibility

Support Performance of safety and risk assessments for medical devices based on the used raw materials, on extractable and leachable chemicals or on biocompatibility studies (ISO 10993 series)
Drive planning, interpretation and evaluation of analytical and biological tests performed by internal or external laboratories under supervision of experienced team members
Assist in compilation of overall biological safety assessment according to ISO 10993-1
Support in deriving biocompatibility strategy details including material characterization, sampling of different product groups during new product developments or material/product changes
Acting as sponsor, study monitor and contact for chemical/ biocompatibility studies in internal and external laboratories
Ensure sufficient support of biocompatibility projects and coordinate how to apply overarching strategies
Align sampling and testing strategies and support product responsibles how to apply these
Coordinate global alignment of laboratory partners (internal and external) as well as methods applied
Overall responsibility for the assigned product groups and related biocompatibility files
Contribute to supplier agreements and specifications for biocompatibility requirements as well as material selection

What we offer

Individual opportunities for self-determined career planning and professional development
A corporate culture in which there is enough room for innovative thinking - to find the best solution together, not the quickest one
A large number of committed people with a wide range of skills, talents and experience
The benefits of a successful global corporation with the collegial culture of a medium-sized company

Fulltime

Instrument Test Technician

Conducts production testing of assembled flow cytometers and related medical dev...

Location

United States , San Jose

Salary:

27.00 - 30.00 USD / Hour

MillenniumSoft Inc

Expiration Date

Until further notice

Requirements

Min educational requirement should be AS in electronics
Some experience in Testing mechanicals (i.e. electronics, lasers)
Some experience in manufacturing work setting
Requires an Associate's degree (A.S.) or equivalent from two-year college or technical school
3+ years related experience in a high tech, manufacturing environment
Ability to effectively communicate information and respond to questions both verbally and in writing
Ability to work with mathematical concepts such as probability and statistical inference, and fundamentals of plane and solid geometry
Ability to apply concepts such as fractions, percentages, ratios, and proportions to practical situations
Good mechanical aptitude, dexterity and hand/eye coordination. Must be able to reach, bend and lift 35 lbs on a daily basis
Experienced in the use of: DVM’s, Oscilloscope and general test equipment

Job Responsibility

Conducts production testing of assembled flow cytometers and related medical device products
May integrate systems and conduct a variety of electronic, mechanical, optical, fluidic and electromechanical activities on systems, subassemblies, and parts to ensure unit functions according to specifications
Will be expected to perform system level and subassembly level troubleshooting to determine root cause, and implement correction of assembly or material defects
Responsible for producing quality products on schedule
Performs instrument optimization functions after final assembly: laser alignment, pressure adjustments, electrical adjustments, etc.
Performs final production testing and inspection to ensure products meet performance specifications and standards
Analyzes test results on defective units to determine root cause of failure
Replaces or repairs defective components or assemblies, processes appropriate paperwork, may return unit to assembly for repair
Compares test results with specifications and records test data and plots test results
Generates required documentation to complete the Device History Record (DHR)

Fulltime

Instrument Test Technician

Conducts production testing of assembled flow cytometers and related medical dev...

Location

United States , San Jose

Salary:

26.00 - 30.00 USD / Hour

MillenniumSoft Inc

Expiration Date

Until further notice

Requirements

3+ years related experience in a high tech, manufacturing environment
Experience working in a medical device manufacturing organization
Experience testing and troubleshooting: laser based optical systems, fluidic systems, digital and analog circuitry
Ability to effectively communicate information and respond to questions both verbally and in writing
Ability to work with mathematical concepts such as probability and statistical inference, and fundamentals of plane and solid geometry
Ability to apply concepts such as fractions, percentages, ratios, and proportions to practical situations
Good mechanical aptitude, dexterity and hand/eye coordination. Must be able to reach, bend and lift 35 lbs on a daily basis
Experienced in the use of: DVM’s, Oscilloscope and general test equipment
Experienced PC or MAC user, familiar with: Word, Excel, Windows and/or MAC OS
Must be willing to be trained in other areas of production where the skill level requirements may be lower

Job Responsibility

Performs instrument optimization functions after final assembly: laser alignment, pressure adjustments, electrical adjustments, etc.
Performs final production testing and inspection to ensure products meet performance specifications and standards
Analyzes test results on defective units to determine root cause of failure
Replaces or repairs defective components or assemblies, processes appropriate paperwork, may return unit to assembly for repair
Compares test results with specifications and records test data and plots test results. Generates required documentation to complete the Device History Record (DHR)
Analyzes test results on defective units to determine root cause of failure. Frequently requires engineering support to resolve complex and unique problems
Must be able to read and understand: detailed test instructions, assembly instructions, work orders, test results, Bills of Materials, Standard Operation Procedures, and all other documentation used to control our products and processes
Confers with engineers, technicians, production personnel, and others regarding testing procedures and results and to resolve problems. Determines, develops and documents troubleshooting techniques
Expected to provide feedback on production and test methods, product design issues, continuously strives to improve product quality and operational efficiency
Will provide support to project teams whose objectives may be: quality improvement, cost reduction, cycle time reduction, reliability improvement, increase operational efficiency, or new product introduction

Fulltime

Experienced Medical Device Product Development Engineer

Life Science Talent

Location:
Denmark , Aarhus

Category:
IT - Software Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
January 05, 2026

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