Senior Project Manager

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🕒 Junho 2

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Fortive

10.000+ funcionários

Fundada em 2016

🏢 Corporativo

⚕️ Seguro de Saúde

💰 Post-IPO Equity em 2020-03

Enterprise • Healthcare Insurance

A Fortive é uma empresa global de tecnologia industrial que se especializa em oferecer soluções avançadas para a área da saúde, soluções operacionais inteligentes e tecnologias de precisão. Com uma equipe de 18. 000 colaboradores, a Fortive trabalha para resolver desafios técnicos complexos, promovendo operações industriais mais seguras, inteligentes e eficientes. A empresa enfatiza sustentabilidade, integridade e melhoria contínua, buscando um futuro mais forte, mais seguro e mais inteligente. A Fortive foi reconhecida como uma das empresas mais responsáveis dos Estados Unidos, demonstrando seu compromisso com impacto social e ambiental positivo.

Descrição

• Lead high-impact medical device development projects across hardware, systems, and consumables from concept through commercialization • Align and lead cross-functional teams across Engineering, Quality, Regulatory, Operations, Marketing, and external partners to deliver integrated project outcomes on time and to standard • Develop and continuously refine integrated project plans, proactively managing scope, schedule, resources, dependencies, and critical path • Proactively identify, assess, and mitigate project risks, prioritizing actions based on business impact • Facilitate structured, data-driven problem solving for complex technical and organizational challenges • Own alignment of projects with evolving business priorities, customer needs, and applicable regulatory and quality system requirements • Own executive-level communication, influence cross-functional alignment, resolve trade-offs, and maintain momentum across projects • Promote a collaborative, high-performance environment that encourages innovation and shared accountability

🎯 Requisitos

• Bachelor’s degree in Engineering, Life Sciences, or a related technical discipline required • 3+ years of project management experience leading end-to-end product development and commercialization of regulated products • 2+ years in the Medical Device industry, including hands-on experience leading projects that resulted in FDA 510(k) clearance • Working knowledge of 21 CFR 820 and ISO 13485 • Demonstrated ability to lead medium to large, global, and interdependent projects in technical domains • Hands-on experience with process improvement and metrics, including use of tools like Jira, Confluence, and Fortive Business Systems (FBS) • Track record of mentoring and developing high-performing project teams

🏖️ Benefícios

• Proactively support ASP’s Environmental, Health and Safety (EHS) Policy • Provide necessary resources and give equal emphasis with other functions • Ensure implementation of safety and environmental procedures, guidelines and standards • Evaluate employee compliance and enforce established safety and environmental procedures and rules • Create a safe work area environment, recognize safe activities, and reward good safety performance • Provide training to employees when needed • Measure safety performance and hold persons accountable for activities and results • Ensure that incidents are investigated to determine root cause, and that corrective actions are taken • Ensure employees wear required protective equipment • Ensure EHS inspections are conducted monthly and corrective actions are implemented

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