Job Function: Research & Development (R&D;)

Location: Hyderabad, Telangana, India

Experience Required: 5–8 Years

Employment Type: Full-time

About the Role

We are looking for an experienced Senior Engineer – Material Compliance to strengthen global material governance and compliance capabilities across medical device products.

The role will focus on ensuring products meet global material regulatory requirements, managing Materials of Concern (MoC) data, and supporting cross-functional teams in material compliance and Environmental Product and Process (EPP) data requirements.

You will work closely with R&D;, QARA, Supply Chain, Procurement and external suppliers to support compliant material selection and disclosure throughout the product lifecycle.

Key Responsibilities

- Lead the development and maintenance of Material Compliance policies, procedures and playbooks to establish consistent global practices.
- Manage and validate material declaration data, including CAS numbers, regulatory status and supplier disclosures.
- Ensure compliance with global regulations such as REACH, RoHS, PFAS, TSCA, Prop 65, MDR and other applicable frameworks.
- Support the creation and governance of the Materials of Concern (MoC) List, incorporating regulatory updates and industry trends.
- Conduct proactive MoC/EPP data gap assessments and coordinate corrective actions with suppliers and internal stakeholders.
- Respond to material compliance inquiries from regulatory authorities, customers and internal teams with accurate and timely information.
- Collaborate with R&D;, QARA, Procurement and Supply Chain to integrate material compliance into design, supplier engagement and quality systems.
- Monitor global regulatory developments and assess their impact on existing and future products.
- Maintain material compliance data systems, dashboards and reporting tools to support transparency, traceability and audit readiness.




- Facilitate internal training and awareness sessions on material compliance requirements and best practices.
- Extract and manage BOM data across PLM and ERP systems, including Agile PLM, ProLima, SAP and NX Teamcenter.

Required Qualifications & Experience

- Bachelor's degree in Materials Science, Chemistry, Chemical Engineering, Mechanical Engineering or a related scientific discipline.
- 5–8 years of experience in Material Compliance, Product Stewardship, Regulatory Material Compliance or related engineering roles.
- Experience in medical devices or other highly regulated industries.
- Hands-on experience with global material regulations, including REACH, RoHS, MDR, PFAS, TSCA, Prop 65, POP, CMR and ED.
- Experience conducting material compliance gap assessments and managing MoC/EPP data.
- Working knowledge of medical device quality and regulatory systems, including ISO 13485 and MDR requirements.
- Experience collaborating with R&D;, QARA, Supply Chain, Procurement and suppliers.

Technical Skills

- Familiarity with material compliance tools such as BoM Check, Assent and iPoint.
- Knowledge of PLM/ERP compliance modules and management of large, complex datasets.
- Strong technical reading, writing and documentation skills.
- Ability to interpret regulatory requirements and translate them into actionable engineering requirements.
- Strong analytical, problem-solving and decision-making capabilities.
- Excellent communication and stakeholder management skills.
- Ability to work independently and collaborate with global, cross-functional teams.

Preferred Qualifications

- Master's degree or advanced certification in a relevant discipline.
- Experience working in a global or international business workplace.
- Experience supporting multiple regions and stakeholders.

Location

Hyderabad, Telangana, India

How to Apply

Interested candidates can share their updated resume at:

[email protected]

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