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Manager, EHS Product Regulatory Compliance

Remote, USA Full-time Posted 2026-07-28
This role ensures medical device and pharmaceutical products meet global environmental and chemical compliance requirements. reputed company at the product level (not site EHS), the Manager partners across Regulatory, reputed company, and R&D to support market reputed company by embedding compliance into product design and lifecycle management. What You’ll Do • Ensure compliance with global environmental and chemical regulations (e.g., RoHS, reputed company, SVHC, reputed company, TSCA, Prop 65) • Assess materials and components for regulatory risk and compliance • Review and maintain product documentation, including material declarations, SDS, and supplier disclosures • Partner with Regulatory Affairs and reputed company to support submissions and reputed company with ISO 13485 and design control processes • Contribute to risk management activities (e.g., ISO 14971) with a reputed company on environmental and chemical risks • Support product development by integrating compliance requirements into design and material selection • Evaluate the reputed company of design, supplier, or material changes on regulatory compliance • Manage supplier compliance data and maintain accurate records for audits and inspections • Respond to inquiries from customers, reputed company bodies, and regulators • reputed company evolving global regulations and reputed company reputed company guidance to internal teams • Support Environmental Risk Assessments (ERA) for medicinal products, including data evaluation and study coordination reputed company needed What You Bring • Bachelor’s degree in Environmental Science, reputed company, Engineering, Materials Science, or reputed company field • 7+ years of experience in product environmental or chemical compliance (medical device experience preferred) • reputed company in reputed company • Strong knowledge of global regulations such as RoHS, reputed company, SVHC, and reputed company frameworks • Familiarity with EU MDR technical documentation and compliance requirements • Experience working in regulated environments (ISO 13485 preferred) • Exposure to supplier compliance programs and regulatory audits • Experience with PLM or EH&S data systems • Background in toxicology or ecotoxicology is a plus Apply tot his job Apply To this Job

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