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Principal Regulatory Affairs Specialist(m/w/x)
Description
You will guide medtech innovations through the regulatory landscape, from providing strategic input on development teams to managing complex submissions for global market clearance.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •BS in Engineering, Life Sciences, Pharmacy, Nursing, Mathematics, or Statistics
- •Preferred graduate degrees in biomedical or clinical engineering
- •Experience in regulated medical device industry
- •Knowledge of pertinent regulatory submission regulations
- •Understanding of clinical and regulatory principles
- •Pragmatic and result-oriented mindset
- •Independent technical writing project management skills
- •Strong interpersonal and challenging skills
- •Strong written and verbal English communication
- •Strong technical writing skills for submissions
- •Proficiency in MS Office
- •Willingness to travel up to 25%
Education
Tasks
- •Provide regulatory input for product development teams
- •Develop submission applications for new or modified devices
- •Participate in meetings with regulatory officials for market approval
- •Interpret medical device regulations for senior management
- •Respond to registration requests from regulatory authorities
- •Review advertising and promotional literature
- •Maintain regulatory files to ensure company compliance
- •Implement initiatives to enhance operational efficiency and quality
- •Develop and review quality system and clinical documentation
- •Collaborate across departments to drive project best practices
- •Ensure local regulatory requirements are met before distribution
Tools & Technologies
Languages
English – Business Fluent
Benefits
Competitive Pay
- •Competitive base salary
Bonuses & Incentives
- •Variable short-term incentives
- •Variable long-term incentives
Informal Culture
- •Supportive, inclusive, collaborative environment
Career Advancement
- •Professional career growth
Modern Equipment
- •Advanced Medical Device environment
Startup Environment
- •State-of-the-Art development process
Other Benefits
- •STARS Program recognition
- Givaudan SAFull-timeOn-siteExperiencedMünchen
- LivaNova Deutschland GmbH
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Principal Regulatory Affairs Specialist(m/w/x)
The AI Job Search Engine
Description
You will guide medtech innovations through the regulatory landscape, from providing strategic input on development teams to managing complex submissions for global market clearance.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •BS in Engineering, Life Sciences, Pharmacy, Nursing, Mathematics, or Statistics
- •Preferred graduate degrees in biomedical or clinical engineering
- •Experience in regulated medical device industry
- •Knowledge of pertinent regulatory submission regulations
- •Understanding of clinical and regulatory principles
- •Pragmatic and result-oriented mindset
- •Independent technical writing project management skills
- •Strong interpersonal and challenging skills
- •Strong written and verbal English communication
- •Strong technical writing skills for submissions
- •Proficiency in MS Office
- •Willingness to travel up to 25%
Education
Tasks
- •Provide regulatory input for product development teams
- •Develop submission applications for new or modified devices
- •Participate in meetings with regulatory officials for market approval
- •Interpret medical device regulations for senior management
- •Respond to registration requests from regulatory authorities
- •Review advertising and promotional literature
- •Maintain regulatory files to ensure company compliance
- •Implement initiatives to enhance operational efficiency and quality
- •Develop and review quality system and clinical documentation
- •Collaborate across departments to drive project best practices
- •Ensure local regulatory requirements are met before distribution
Tools & Technologies
Languages
English – Business Fluent
Benefits
Competitive Pay
- •Competitive base salary
Bonuses & Incentives
- •Variable short-term incentives
- •Variable long-term incentives
Informal Culture
- •Supportive, inclusive, collaborative environment
Career Advancement
- •Professional career growth
Modern Equipment
- •Advanced Medical Device environment
Startup Environment
- •State-of-the-Art development process
Other Benefits
- •STARS Program recognition
About the Company
LivaNova Deutschland GmbH
Industry
Healthcare
Description
The company focuses on developing innovative medical technologies to improve patient outcomes.
- Givaudan SA
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