Posted:5 days ago|
Platform:
On-site
Full Time
As a Regulatory & Compliance Engineer within the STET Grooming & Beauty (GB) team, you will play a key role in ensuring our products meet global regulatory, safety, and compliance standards throughout their lifecycle. You will support product registrations, safety certifications, documentation, and regulatory assessments while partnering closely with R&D, Quality, LCM, and Manufacturing teams.
Your role:
Manage and support regulatory activities for product changes and lifecycle maintenance.
Prepare, submit, and maintain regulatory documentation, approvals, and compliance records.
Review product labeling, packaging, and marketing materials to ensure regulatory compliance.
Track and interpret relevant regulatory changes and support their deployment across teams.
Coordinate product testing and safety evaluations, including engagement with external test houses.
Ensure adherence to internal policies, global standards, and quality system requirements.
Support internal and external audits with accurate, audit‑ready documentation.
Collaborate closely with cross‑functional teams to proactively manage compliance risks.
You're the right fit if you have :
Bachelor's / Master's Degree in Biomedical Engineering / any Engineering background.
Minimum required Experience:
Minimum 8 years of experience in areas such as Regulatory Affairs, Quality Compliance, Product Development in Medical Devices Industry
Preferred Skills: highest priority
Preferred Skills: secondary priority
How we work together
We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week.
Onsite roles require full-time presence in the company’s facilities.
Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations.
Indicate if this role is an office/field/onsite role.
Philips
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