ZipRecruiter

Log In

1

Medical Device Germany Jobs in Wisconsin (NOW HIRING)

All JobsMedical Device Germany JobsMedical Device Germany Jobs in Wisconsin

Medical Device Germany information

What are medical device jobs in Germany?

Medical device jobs in Germany involve working with the development, manufacturing, regulation, sales, and support of medical devices such as diagnostic equipment, implants, and surgical instruments. These roles can range from engineering and quality assurance to regulatory affairs, sales, and technical support. Germany has a strong medical technology sector, so there are diverse opportunities in both local companies and international firms with operations in the country.

What are some typical challenges faced by professionals working in the medical device industry in Germany?

Professionals in the medical device industry in Germany often navigate a highly regulated environment, as compliance with both European MDR (Medical Device Regulation) and German-specific standards is essential. Adapting to frequent regulatory changes and ensuring thorough documentation can be demanding. Additionally, collaborating effectively with cross-functional teams—such as R&D, quality assurance, and sales—is crucial for bringing products to market successfully. Language proficiency and understanding local healthcare systems also play a significant role in daily operations.

What are the key skills and qualifications needed to thrive as a medical device sales representative in Germany, and why are they important?

To thrive as a Medical Device Sales Representative in Germany, you need a background in life sciences or engineering, strong sales experience, and familiarity with medical regulations. Proficiency with CRM systems, product demonstration tools, and knowledge of EU MDR (Medical Device Regulation) are typically required. Exceptional interpersonal skills, negotiation abilities, and fluency in both German and English help build trust and effectively communicate with healthcare professionals. These competencies are crucial for navigating complex sales cycles, ensuring compliance, and achieving sales targets in a highly regulated market.

What is the difference between Medical Device Germany vs Medical Device Technician?

AspectMedical Device GermanyMedical Device Technician
CertificationsRelevant certifications like ISO standards, CE marking, and industry-specific trainingTechnical certifications, such as biomedical equipment technician (BMET) or similar
Work EnvironmentManufacturing plants, quality assurance labs, regulatory agencies in GermanyHospitals, clinics, repair centers, and manufacturing facilities
Employer & Industry UsageMedical device manufacturers, regulatory bodies, and healthcare companies in GermanyHealthcare facilities, service providers, and medical equipment companies

Medical Device Germany professionals focus on regulatory compliance, quality assurance, and manufacturing standards within Germany's medical device industry. In contrast, Medical Device Technicians primarily handle installation, maintenance, and repair of medical equipment in clinical settings. Both roles require technical skills but differ in scope and work environment.

What job categories do people searching Medical Device Germany jobs in Wisconsin look for?

The top searched job categories for Medical Device Germany jobs in Wisconsin are:

What cities in Wisconsin are hiring for Medical Device Germany jobs?

Cities in Wisconsin with the most Medical Device Germany job openings:

Medical Device Germany jobs near you

Quality Engineer Associate I

Merz North America

Franksville, WI • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 4 days ago

Job description

About Us
Founded in 1908, Merz is a successful, family-owned specialty healthcare company with a rich history. As a leading global aesthetics business, our award-winning portfolio of injectables, devices, and skincare products empowers healthcare professionals to enhance confidence through aesthetic medicine. Our purpose is to fuel confidence by helping people look better, feel better, and live better. We believe you do not have to choose between living life and making a living. Live your best life with Merz Aesthetics.
A Brief Overview
This position supports a wide array of activities related to: Nonconformance Records (NCR), Corrective and Preventive Action (CAPA), Change Control, Product Surveillance, Design Control, New Markets and Risk Management. Support the operation of Manufacturing and Quality activities in relation to compliance to Quality Standards and Regulations and recommend where corrections or improvements are indicated. Provide direct support to Quality personnel regarding operation of the department and Quality System. Provide support to other departmental activities as directed.
What You Will Do
  • NCR and CAPA activities Execute Investigations, Root Cause Analysis, Correction, Corrective and Preventive Action activities in accordance with the Merz North America Quality System for NCRs and CAPAs including: capturing data and investigations associated with product deviations, product nonconformances, CAPAs, scrap, and rework, and analyzing the data for the reasons of Quality Improvement and reporting.
  • Support Change Control activities Originate, review, and approve internal operating procedures and specifications through the Document Change process.
  • Support Product Surveillance activities Support Product Surveillance through review and ownership of data/trend evaluations and investigations associated with product and patient complaints, analyzing the data for the reasons of Quality Improvement and reporting.
  • Support New Markets activities Support New Markets activities including: management of new markets samples process; coordination between new markets group in Germany and WI Tech Ops to manufacture samples; filing of applicable new markets documentation in the Design History File (DHF).
  • Support Risk Management activities Support Risk Management activities including: data preparation for annual product risk file review; review internal documents (IFU, CER, etc) for annual product risk file review; management and preparation of event-based reviews; review and coordination of quality activities related to pFMEA risk matrices.
  • Supports Internal and Vendor Audit Functions Supports Internal and Vendor Audit Functions as needed.
  • R&D Support Provide assistance, as needed, to the R&D department in the development and validation of new products.
  • Process improvement initiatives Coordinates process improvement initiatives for the Quality Department.
  • Adherence to regulations Assist with adherence to all Federal, State, and Local Regulations controlling the manufacture of medical devices.
  • Other duties as assigned Provides support to Quality Management personnel and perform other duties as assigned.

Minimum Requirements
  • Bachelor's Degree or equivalent experience

Preferred Qualifications
  • Bachelor's Degree BS/BA in Engineering or Physical Science
  • GLP/GMP experience
  • Medical Device experience

Technical & Functional Skills
  • Familiarity with cGMP regulations and FDA/USP/EP/BP/ICH guidelines.
  • Quality experience may include quality testing (analytical chemistry/microbiology), QA/Regulatory, and/or Validation.
  • Experience with FDA, European agency regulations, cGMP regulations, Laboratory Information.
  • Management Systems (LIMS) and Quality Management software is highly preferred.
  • Knowledge of quality systems, quality techniques, current regulatory requirements and technical issues resolution.
  • Proficiency with all equipment in the lab, as well as equipment preventative maintenance and method/process troubleshooting.
  • Familiarity with general laboratory and incoming supply inspection testing.
  • Computer skills including those associated with the word processing, spread sheet programs, databases and statistical analysis.
  • Ability to prepare testing protocols and reports, operating documents and procedures.
  • Ability to work with little or no supervision and make effective decisions.

Benefits
  • Comprehensive Medical, Dental, and Vision plans
  • 20 days of Paid Time Off
  • 15 paid holidays
  • Paid Sick Leave
  • Paid Parental Leave
  • 401(k)
  • Employee bonuses
  • And more!

Your benefits and PTO start the date you're hired with no waiting period!
This position is not eligible for employer-sponsored work authorization. Applicants must be legally authorized to work in the United States without the need for current or future employer-sponsored work authorization.
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

Apply