Main responsibilities:
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Act as the key medical counterpart for gynecology-related products, including OTC and food supplements as well as medical devices
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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

