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Senior Manager Medical Affairs(m/w/x)
Description
In this role, you will leverage your clinical and technical expertise to guide product development and training initiatives. Your day-to-day responsibilities will involve collaborating with cross-functional teams, addressing clinical challenges, and ensuring compliance with industry standards.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Excellent written, oral communication, and organizational skills
- •Effective presentation and teaching skills
- •Self-motivated, independent, multi-tasking, team-oriented
- •Degree in related clinical discipline or equivalent
- •Experienced Nurse/Practitioner with surgical device background
- •Active license or regional equivalent in good standing
- •Minimum 5 years of related Surgical experience
- •Experience with surgical tables, lights, and accessories
- •Knowledge of Baxter products and competitive products
- •In-depth knowledge of class I and II device registration
- •Bachelor’s degree or advanced degree in Health or Science field
- •Minimum 5 years of relevant Industry experience
Education
Work Experience
5 years
Tasks
- •Serve as the medical device subject matter expert for product development and risk assessment
- •Devise innovative solutions for clinical and technical challenges in medical devices
- •Provide timely clinical expertise to various functional areas based on objective evidence
- •Incorporate voice of the customer and clinical experience into product design
- •Develop risk assessments and quality standards for product design history files
- •Understand EMDUR clinical documentation requirements for safety and performance
- •Create and deliver medical device training programs, including eLearning
- •Train internal customers on product applications and regional differences
- •Support the product implementation process and controlled launch planning
- •Stay updated on published literature related to clinical trends and therapies
- •Adhere to complaint and adverse event handling requirements
- •Support legal, regulatory, and quality requirements in R&D and product lifecycle management
- •Maintain compliance with standard operating procedures
- •Demonstrate clinical and technical core competencies for related products
Languages
German – Business Fluent
English – Business Fluent
Benefits
Retirement Plans
- •Company pension scheme
Competitive Pay
- •Share plan for employees
More Vacation Days
- •30 days vacation
- •Special leave
Other Benefits
- •Additional insurance
Learning & Development
- •Professional training opportunities
Flexible Working
- •Flexible workplace policy
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Senior Manager Medical Affairs(m/w/x)
The AI Job Search Engine
Description
In this role, you will leverage your clinical and technical expertise to guide product development and training initiatives. Your day-to-day responsibilities will involve collaborating with cross-functional teams, addressing clinical challenges, and ensuring compliance with industry standards.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Excellent written, oral communication, and organizational skills
- •Effective presentation and teaching skills
- •Self-motivated, independent, multi-tasking, team-oriented
- •Degree in related clinical discipline or equivalent
- •Experienced Nurse/Practitioner with surgical device background
- •Active license or regional equivalent in good standing
- •Minimum 5 years of related Surgical experience
- •Experience with surgical tables, lights, and accessories
- •Knowledge of Baxter products and competitive products
- •In-depth knowledge of class I and II device registration
- •Bachelor’s degree or advanced degree in Health or Science field
- •Minimum 5 years of relevant Industry experience
Education
Work Experience
5 years
Tasks
- •Serve as the medical device subject matter expert for product development and risk assessment
- •Devise innovative solutions for clinical and technical challenges in medical devices
- •Provide timely clinical expertise to various functional areas based on objective evidence
- •Incorporate voice of the customer and clinical experience into product design
- •Develop risk assessments and quality standards for product design history files
- •Understand EMDUR clinical documentation requirements for safety and performance
- •Create and deliver medical device training programs, including eLearning
- •Train internal customers on product applications and regional differences
- •Support the product implementation process and controlled launch planning
- •Stay updated on published literature related to clinical trends and therapies
- •Adhere to complaint and adverse event handling requirements
- •Support legal, regulatory, and quality requirements in R&D and product lifecycle management
- •Maintain compliance with standard operating procedures
- •Demonstrate clinical and technical core competencies for related products
Languages
German – Business Fluent
English – Business Fluent
Benefits
Retirement Plans
- •Company pension scheme
Competitive Pay
- •Share plan for employees
More Vacation Days
- •30 days vacation
- •Special leave
Other Benefits
- •Additional insurance
Learning & Development
- •Professional training opportunities
Flexible Working
- •Flexible workplace policy
About the Company
Baxter Medical Systems GmbH + Co. KG
Industry
Healthcare
Description
Das Unternehmen bietet innovative Medizintechnikprodukte und Lösungen, die die Effizienz und Patientensicherheit im Gesundheitswesen verbessern.
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