- Bachelor's degree in Materials Science, Chemistry, Chemical Engineering, Mechanical Engineering, or related scientific discipline.
Experience
- 2 to 5 years of experience in material compliance, product stewardship, regulatory support, or a related engineering function within a regulated industry.
- Internship or final-year project experience in a regulated or data-intensive engineering environment is an advantage.
- Working knowledge of global material regulations including REACH, RoHS, PFAS, TSCA, Prop 65, and
EU MDR chemical safety requirements (Engineer level).
- Hands-on experience with PLM or ERP systems such as Agile PLM, ProLima, SAP, or NX Teamcenter for BOM data extraction and management (Engineer level; training provided for Junior Engineer).
- Experience with material compliance data systems such as Assent, iPoint, or BoM Check preferred for
Engineer level.
- Exposure to medical device quality systems and documentation standards is an advantage.
Required Skills
- Strong technical background in R&D; engineering disciplines.
- Strong attention to detail and commitment to data accuracy — the quality of compliance data depends on the rigour applied at this level.
- Good organisational skills with the ability to manage structured, process-driven tasks methodically and consistently.
- Comfortable working with large datasets across spreadsheets, databases, and engineering systems.
- Transparent written and verbal communication in English for supplier coordination, documentation, and internal reporting.
- Team-oriented, reliable, and proactive in flagging issues and seeking guidance when needed.
- Willingness to learn and develop technical knowledge in an evolving regulatory and compliance environment.
- Ability to handle high-volume data tasks with consistent quality and thoroughness under guidance.