Description
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:**
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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!**