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Straumann Group in Curitiba seeks a Product Development LCM Specialist to drive lifecycle management of marketed dental implants and instruments, ensuring ongoing compliance and cost improvements.
You will lead cross-functional projects, perform technical assessments, maintain DHF documentation, and support regulatory submissions under MDR, FDA, ISO standards. The role emphasizes collaboration with dentists, engineers, and Operations, with strong opportunities for growth.
Opportunity based in CIC.
The Product Development LCM Specialist at the Straumann Development Center, plays a crucial role in ensuring the ongoing success of dental implant products that are already released and available on the market. This role focuses on maintaining, improving, optimizing, and supporting products throughout their commercial life cycle. This includes evaluating product and design changes, assessing design optimization opportunities, and identifying COGS and cost improvement opportunities.
The specialist performs technical assessments for product and design changes and ongoing product improvements, ensuring continued compliance with regulatory standards. Collaboration with dentists, engineers, materials scientists, and Operations is essential for addressing clinical needs, manufacturing requirements, product performance, and market demands. Additionally, the role includes preparing and updating technical and product documentation for life cycle activities and regulatory submissions to ensure compliance with FDA and ISO standards. The specialist supports root cause investigations, using feedback and operational information to implement continuous improvements and maintain product reliability and user satisfaction.
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At Straumann Group, we believe in the power of diversity. That’s why all our opportunities are open to everyone, regardless of gender, race, sexual orientation, religion, nationality, age, or disability.
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