Regulatory and Compliance Engineer
Philips
Regulatory and Compliance Engineer
Job Description
Job Title
Regulatory and Compliance EngineerJob Description
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
• Technical Product Documentation
• Regulatory Submission Documentation
• Conformity Assessment
• Regulatory Requirements (particularly on major markets and jurisdictions, e.g. US CFR, EU MDR)
• Standards (e.g. 60601 series, 14971, 62304)
• Regulatory Compliance activities
• Document Review / Auditing
• Product Registrations
• Product Labeling
• Continuous Improvement
• People Management
Preferred Skills: secondary priority
• Strategy Implementation
• Stakeholder Management
• Regulatory Intelligence
• Risk Mitigation Strategies
• Project Management
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.
About Philips
We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others.
• Learn more about our business.
• Discover our rich and exciting history.
• Learn more about our purpose.
If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our culture of impact with care here.
Locations
- Pune, Maharashtra, India
Salary
800,000 - 2,000,000 INR / yearly
Source: ai estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Technical Product Documentationintermediate
- Regulatory Submission Documentationintermediate
- Conformity Assessmentintermediate
- Regulatory Requirements (US CFR, EU MDR)intermediate
- Standards (60601 series, 14971, 62304)intermediate
- Regulatory Complianceintermediate
- Document Review/Auditingintermediate
- Product Registrationsintermediate
- Product Labelingintermediate
- Continuous Improvementintermediate
- People Managementintermediate
Required Qualifications
- Bachelor's/Master's in Biomedical Engineering or any Engineering (experience)
- Minimum 8 years experience in Regulatory Affairs, Quality Compliance, or Product Development in Medical Devices (experience)
Responsibilities
- Manage regulatory activities for product changes and lifecycle maintenance
- Prepare, submit, and maintain regulatory documentation
- Review product labeling, packaging, and marketing materials
- Track and interpret regulatory changes
- Coordinate product testing and safety evaluations
- Ensure adherence to policies and standards
- Support audits
- Collaborate with cross-functional teams
Tags & Categories
Answer 10 quick questions to check your fit for Regulatory and Compliance Engineer @ Philips.
Regulatory and Compliance Engineer
Philips
Regulatory and Compliance Engineer
Job Description
Job Title
Regulatory and Compliance EngineerJob Description
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
• Technical Product Documentation
• Regulatory Submission Documentation
• Conformity Assessment
• Regulatory Requirements (particularly on major markets and jurisdictions, e.g. US CFR, EU MDR)
• Standards (e.g. 60601 series, 14971, 62304)
• Regulatory Compliance activities
• Document Review / Auditing
• Product Registrations
• Product Labeling
• Continuous Improvement
• People Management
Preferred Skills: secondary priority
• Strategy Implementation
• Stakeholder Management
• Regulatory Intelligence
• Risk Mitigation Strategies
• Project Management
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.
About Philips
We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others.
• Learn more about our business.
• Discover our rich and exciting history.
• Learn more about our purpose.
If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our culture of impact with care here.
Locations
- Pune, Maharashtra, India
Salary
800,000 - 2,000,000 INR / yearly
Source: ai estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Technical Product Documentationintermediate
- Regulatory Submission Documentationintermediate
- Conformity Assessmentintermediate
- Regulatory Requirements (US CFR, EU MDR)intermediate
- Standards (60601 series, 14971, 62304)intermediate
- Regulatory Complianceintermediate
- Document Review/Auditingintermediate
- Product Registrationsintermediate
- Product Labelingintermediate
- Continuous Improvementintermediate
- People Managementintermediate
Required Qualifications
- Bachelor's/Master's in Biomedical Engineering or any Engineering (experience)
- Minimum 8 years experience in Regulatory Affairs, Quality Compliance, or Product Development in Medical Devices (experience)
Responsibilities
- Manage regulatory activities for product changes and lifecycle maintenance
- Prepare, submit, and maintain regulatory documentation
- Review product labeling, packaging, and marketing materials
- Track and interpret regulatory changes
- Coordinate product testing and safety evaluations
- Ensure adherence to policies and standards
- Support audits
- Collaborate with cross-functional teams
Tags & Categories
Answer 10 quick questions to check your fit for Regulatory and Compliance Engineer @ Philips.