Environmental Compliance Program Manager

Company Description

It started with a simple idea: what if surgery could be less invasive and recovery less painful? Nearly 30 years later, that question still fuels everything we do  a global leader in robotic-assisted surgery and minimally invasive care, our technologies—like the da Vinci surgical system and Ion—have transformed how care is delivered for millions of patients worldwide.

We're a team of engineers, clinicians, and innovators united by one purpose: to make surgery smarter, safer, and more human. Every day, our work helps care teams perform with greater precision and patients recover faster, improving outcomes around the world.

The problems we solve demand creativity, rigor, and collaboration. The work is challenging, but deeply meaningful-because every improvement we make has the potential to change a life.

If you're ready to contribute to something bigger than yourself and help transform the future of healthcare, you'll find your purpose here.

Primary Function of the Position

Responsibilities include supporting Intuitive's Environmental Management System with delivery and execution of related projects including the administration and maturity of Restricted/Regulated Substance Database, Battery and Packaging program management, collaboration tools and development of operational reports and tools for use by the broader functional and regional teams. This role is intended to help Intuitive demonstrate compliance to its Environmental and Social Responsibility competencies.

• Partner cross functionally with regional regulatory teams as well as Product Operations teams to develop and design programs in accordance with various regulatory requirements
• Effectively manages the execution of the Regulated Materials process ensuring compliance to identified regulations/directives
• Ensure products and parts are scoped appropriately
• Partner cross functionally within the organization to drive conformance and compliance
• Ensure the right support is given from/to other departments to accomplish the goals
• Ensuring process compliance to applicable regulations, directives, and standards (e.g. PPWR, Batteries, WEEE, etc...)
• Drive maturity of Extended Producer Responsibility Process
• Continuously monitor compliance to applicable regulations/directives
• In partnership with cross functional teams, define strategies to mitigate compliance issues.
• Support business functions in creating a defensible, documented compliance package
• Additional tasks may be assigned as needed

• Minimum 5 years relevant experience
• Data management, database creation, or data and information modeling
• Deep understanding of product compliance regulations in regulated industry required
• Ability to manage multiple objectives and priorities concurrently
• Familiarity with key business applications such as SAP and Agile PLM
• Exceptional knowledge of global Environmental Compliance Directives, Regulations and Standards including but not limited to: EU RoHS, Packaging, Battery, WEEE, REACH, Prop 65 and Conflict Minerals.
• Experience analyzing compliance data to verify accuracy
• Product, supply chain, and design control in a medical device manufacturer (such as BOM, COTS, Custom, ASL, AML, etc...)
• Translating regulatory documents to extrapolate business requirements and or product requirements

• Exceptional organizational, data entry, decision making and analytical skills.
• Excellent communication skills, both written and verbal.
• Cross functional teamwork across all levels of the organization
• Demonstrated self-starting, results driven, high energy level and ability to focus
• Self-motivated and resourceful
• Ability to manage multiple objectives and priorities concurrently
• Excellent analytical skills,…