About the Company: ROOTT is a fast-growing dental implant company delivering innovative, precision-engineered implant solutions for clinicians worldwide. With a strong focus on quality, R&D, and professional education, ROOTT supports dentists with reliable products and practical solutions designed to improve patient outcomes.
We are seeking a highly strategic and detail-oriented Product Specialist to lead
product commercialization, portfolio development, clinical product communication,
and regulatory coordination for our growing global medical device portfolio.
This role acts as the bridge between R&D, Manufacturing, Quality, Regulatory,
Marketing, Sales, and Clinical teams to ensure products are market-ready, globally
compliant, and commercially successful. The ideal candidate combines strong
technical knowledge with commercial understanding and cross-functional leadership
capabilities.
Key Responsibilities
Product Portfolio & Commercialization
Lead preparation and market readiness of new and existing products.
Develop and maintain product descriptions, technical specifications, usage guidelines, and supporting documentation.
Support New Product Introduction (NPI) launches in collaboration with Sales and Marketing teams.
Conduct portfolio reviews and provide recommendations for product improvements,
updates, launches, extensions, or phase-outs.
Translate technical product information into customer-focused commercial tools and sales enablement materials.
Product Content & Visual Coordination
Coordinate with designers, illustrators, and technical teams for:
o Product renders
o 3D animations
o Product images
o Instruction manuals
o Demonstration materials
o IFU and training content
Ensure all visual and technical materials align with product specifications and regulatory
standards.
Clinical & Customer Intelligence
Collect and analyze customer, distributor, clinician, and internal stakeholder feedback.
Collaborate with Key Opinion Leaders (KOLs) to support clinical validation and product
positioning.
Prepare product recommendations and technical responses for clients and internal teams.
Support post-market product evaluation and continuous improvement initiatives.
Regulatory & Compliance Coordination
Manage and maintain product-related documentation and technical records.
Coordinate with QA and Regulatory teams regarding:
o Product changes
o Regulatory documentation
o Technical files
o UDI/GTIN assignments and updates
o Global registration support
Participate in internal and external audits as required.
Support compliance initiatives related to MDR, CE, FDA, and other applicable regulatory
frameworks.
Cross-Functional Collaboration
Work closely with Manufacturing, Engineering, QA, CRM, and Marketing teams to identify
product issues and improvement opportunities.
Provide technical product training internally and externally, including factory training
sessions.
Support exhibitions, product demonstrations, clinical events, and promotional campaigns.
Key Skills & Competencies
Strong understanding of medical device products and commercialization processes.
Knowledge of regulatory standards and documentation requirements (MDR, CE, FDA, UDI,
GTIN preferred).
Ability to translate technical information into commercial and clinical communication.
Excellent project coordination and stakeholder management skills.
Strong analytical and problem-solving abilities.
High attention to detail and documentation accuracy.
Effective communication and presentation skills.
Ability to manage multiple projects in a fast-paced environment.
Qualifications & Experience
Bachelor’s degree in Biomedical Engineering, Life Sciences, Dentistry, Healthcare, or related field.
3+ years of experience in product management, product specialization, regulatory
coordination, or medical device commercialization.
Experience within the dental, implantology, or medical device industry preferred.
Familiarity with product lifecycle management and technical documentation systems is an
advantage.
Key Performance Indicators (KPIs)
Successful launch and commercialization of new products.
Timely completion and maintenance of regulatory and technical documentation.
Product portfolio growth and optimization.
Resolution of technical and product-related inquiries within defined timelines.
Reduction of product-related issues through continuous improvement initiatives.
High-quality support for sales, marketing, and clinical teams.
Why Join Us
Opportunity to work in a rapidly growing global medical device organization.
Strategic role with cross-functional leadership exposure.
Direct impact on innovation, product success, and market growth.
Collaborative and dynamic work environment focused on continuous improvement and
innovation.
Job Types: Full-time, Permanent
Work Location: In person
