- Lead the development and management of clinical study protocols, ensuring full compliance with international regulatory standards
- Oversee clinical evaluations and post-market surveillance activities, ensuring adherence to relevant medical and regulatory requirements
- Prepare and submit clinical papers and documentation to support product registrations and regulatory submissions
- Monitor and manage ongoing clinical trials, ensuring compliance with regulatory requirements and adherence to study protocols
- Conduct risk analysis and provide expert recommendations on clinical safety issues for both new and existing products
- Train and collaborate with internal teams on the latest clinical insights and regulatory standards
- Master’s degree or PhD (preferred) in life sciences, healthcare, or a related field
- Several years of experience in clinical affairs within the medical device industry
- Strong knowledge of international regulatory requirements and proven experience in clinical trial management
- Excellent organizational and project management skills, with the ability to work cross-functionally in a dynamic environment
- Hands-on style and can-do-mentality
- Outstanding communication skills, with fluency in English (both written and verbal)
- High attention to detail, with excellent analytical and problem-solving skills
- A collaborative mindset with the ability to work well in teams and contribute to collective goals
- Either located in germany or israel
- Willingness for occasional travel
- A diverse and challenging role within a leading, growth-oriented company at the forefront of the medical field
- A collaborative and respectful working environment with flat hierarchies and short decision-making paths
- Long-term, secure career prospects in an innovative and forward-thinking industry
- Company-sponsored occupational pension schemes
- Monthly allowances via the givve® Card, a voucher-based employee benefit system
- Access to corporate benefits, offering exclusive discounts on various products and services
- Special bonuses for service anniversaries (5, 10, 15, and 20 years) and on your birthday
- Flexible working hours and remote working options (home office)
- Comprehensive onboarding and continuous opportunities for personal and professional development
Elevate your career with a role that offers both strategic impact and operational involvement at a global leader in medical aesthetics. Our HR department will be happy to answer your questions from Monday to Friday between 8:00 am and 5:00 pm on +49 6071 9863 1718 or by e-mail at Bewerbung[at]polytechhealth.com.
POLYTECH Health & Aesthetics is one of the world's leading developers and manufacturers of soft tissue implants for reconstructive and aesthetic plastic surgery, and the only company of its kind in Germany. At our state-of-the-art production facility in Dieburg, just south of Frankfurt (Main), we produce innovative products that are sold in over 80 countries worldwide.
Due to our continuous growth, we are seeking dedicated professionals to strengthen our dynamic team. Join us and become part of a forward-thinking and innovative company where your contributions will have a global impact.
