




Job Summary: We are seeking a Senior Project Manager to manage and implement Lifecycle Management (LCM) and New Product Development (NPD) projects, focusing on direct materials and components manufactured by external partners, acting as a project leader within a development team and applying engineering principles. Key Highlights: 1. LCM and NPD project leadership 2. Experience with direct materials and external components 3. Application of engineering principles in development **Description:** ---------------- We seek a professional experienced in managing and implementing **Lifecycle Management (LCM) and New Product Development (NPD)** projects, with focus on direct materials and components manufactured by external partners. The role involves serving as a project leader integrated into a development team, applying engineering principles. **Position:** Senior NPD Project Manager **Salary:** R$ 6.900,00 per month + R$ 1.800,00 in flexible benefits per month **Employment Type:** CLT **Work Mode:** Hybrid in São José dos Campos – SP **Standard CLT Benefits:** **Health and Dental Insurance:** Bradesco, with no employee deduction or co-payment, extended to immediate dependents at differentiated rates; **Mobility Allowance:** R$ 200.00 per month; **Meal Voucher:** R$ 27.55 per day; **AS2 Academy:** R$ 500.00 per year for training and certifications; **Flexible CLT Benefits:** **Education Allowance:** R$ 350.00 per month; **Health/Wellness Allowance:** R$ 1.050,00 per month; **Culture Allowance:** R$ 400.00 per month; Best of all, this package grows with you and your career, offered according to your position. **Requirements:** * Bachelor’s degree in Mechanical Engineering, Production Engineering, or related fields; * Postgraduate degree/MBA in Project Management or Engineering. * Advanced English proficiency; * Experience in project coordination; * FPX, Lean, Six Sigma, Continuous Improvement, or Process Excellence. * **Manufacturing process knowledge (mandatory).** * Negotiation, conflict resolution, strategic planning, and assertive communication skills. **Main Responsibilities:** * Preparation of technical protocols and reports ensuring compliance with franchise procedures and regulations. * Evaluation and updating of documentation for changes in direct materials and components, including creation or modification of component drawings and specifications. * Support for supplier process qualification and internal process verification/validation activities. * Experience in planning and executing design changes and process confirmation projects. * Advanced understanding of GMPs, ISO standards, and related regulations. * Hands-on experience with agile methodologies: FPX, Lean, Six Sigma, Continuous Improvement, or Process Excellence. * Experience in the medical device industry or other regulated industries. **If you’re excited about this challenge, join us!**


