Main responsibilities:
- 
	
Act as the key medical counterpart for gynecology-related products, including OTC and food supplements as well as medical devices
 - 
	
Provide medical input into portfolio strategy and management, aligned with the company's global goals
 - 
	
Participate in shaping the R&D and clinical development strategy for gynecology
 - 
	
Support product lifecycle management with scientific and medical expertise across Rx, OTC, and medical device categories
 - 
	
Ensure compliance with relevant regulations and Quality Systems, particularly MDR for medical devices
 - 
	
Develop and evaluate clinical development plans for non-prescription and medical device products
 - 
	
Provide medical evaluation and interpretation of clinical and pre-clinical data for potential in-licensing projects
 - 
	
Prepare innovative scientific-medical concepts to support strategic decision-making
 - 
	
Collaborate with internal stakeholders (e.g. Regulatory, R&D, Business Development) and support cross-functional alignment
 - 
	
Monitor the scientific landscape, standard of care, and unmet medical needs in gynecology
 - 
	
Participate in internal and external medical communication, including presentations and training sessions
 
- 
	
Medical or Pharma degree with at least 5 years of experience
 - 
	
Clinical development experience, preferably in a pharmaceutical or medical device environment
 - 
	
Experience with medical devices is considered an advantage
 - 
	
In-depth knowledge of scientific research methodology, literature review, and clinical trial design
 - 
	
Fluency in English (business and scientific)
 - 
	
High degree of independence, strong communication and networking skills
 - 
	
Flexible, accurate, quality- and process-oriented working style
 - 
	
Demonstrated ability to work ethically and cross-functionally, with a strategic mindset
 
Main responsibilities:
- 
Act as the key medical counterpart for gynecology-related products, including OTC and food supplements as well as medical devices
 - 
Provide medical input into portfolio strategy and management, aligned with the company’s global goals
 - 
Participate in shaping the R&D and clinical development strategy for gynecology
 - 
Support product lifecycle management with scientific and medical expertise across Rx, OTC, and medical device categories
 - 
Ensure compliance with relevant regulations and Quality Systems, particularly MDR for medical devices
 - 
Develop and evaluate clinical development plans for non-prescription and medical device products
 - 
Provide medical evaluation and interpretation of clinical and pre-clinical data for potential in-licensing projects
 - 
Prepare innovative scientific-medical concepts to support strategic decision-making
 - 
Collaborate with internal stakeholders (e.g. Regulatory, R&D, Business Development) and support cross-functional alignment
 - 
Monitor the scientific landscape, standard of care, and unmet medical needs in gynecology
 - 
Participate in internal and external medical communication, including presentations and training sessions
 
- 
Medical or Pharma degree with at least 5 years of experience
 - 
Clinical development experience, preferably in a pharmaceutical or medical device environment
 - 
Experience with medical devices is considered an advantage
 - 
In-depth knowledge of scientific research methodology, literature review, and clinical trial design
 - 
Fluency in English (business and scientific)
 - 
High degree of independence, strong communication and networking skills
 - 
Flexible, accurate, quality- and process-oriented working style
 - 
Demonstrated ability to work ethically and cross-functionally, with a strategic mindset
 

