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Regulatory Affairs Manager

Philips

Regulatory Affairs Manager

full-timePosted: Jan 13, 2026

Job Description

Job Title

Regulatory Affairs Manager

Job Description

Job title:
Regulatory Affairs Manager

Your role:
• The greater impact of this role. 

This role ensures that Philips’ products comply with global regulatory standards, enabling safe and effective healthcare solutions. This directly impacts patient safety, accelerates product approvals, and supports innovation in medical technology.

• Detail elements of the team and stakeholders for this role. 

You’ll collaborate cross-functionally with Regulatory Affairs Specialists, Quality Assurance, R&D and Engineering, Clinical Affairs, Marketing and Product Management, to ensure compliance throughout the product lifecycle.

• What are the professional and personal opportunities for development within this role?  

Exposure to global regulatory frameworks (FDA, EU MDR, ISO standards), Opportunities for international collaboration and cultural exposure

• From Health and wellness programs to Work-life balance initiatives, a career at Philips comes with all sorts of wonderful benefits. Be sure to speak to your recruiter about benefits in your region. 

You're the right fit if:  
1. Experience: Typically requires 10-15 years of experience in the medical device industry, with a proven track record of successful submissions.
2. Skills: USFDA 510k submission, CE certification, EU MDR, ISO 13485, ISO 14971, 21 CFR 820, Health Canada & CDSCO submission, medical device rules 2017, CAPA
3. Education: Bachelor’s degree in a scientific field (Pharmacy, Biology, or Chemistry) or Engineering; a master’s degree or Regulatory Affairs Certification (RAC) is highly preferred.
4. Anything else: Capacity to manage multiple high-stakes projects simultaneously under strict deadlines.

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

Estimated Salary Rangemedium confidence

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

  • USFDA 510k submissionintermediate
  • CE certificationintermediate
  • EU MDRintermediate
  • ISO 13485intermediate
  • ISO 14971intermediate
  • 21 CFR 820intermediate
  • Health Canada & CDSCO submissionintermediate
  • CAPAintermediate

Required Qualifications

  • 10-15 years experience in medical device industry (experience)
  • Bachelor’s degree in scientific field (Pharmacy, Biology, Chemistry) or Engineering (experience)
  • Master’s degree or RAC preferred (experience)
  • Manage multiple high-stakes projects under deadlines (experience)

Responsibilities

  • Ensure products comply with global regulatory standards
  • Collaborate with QA, R&D, Engineering, Clinical Affairs, Marketing

Benefits

  • general: Health and wellness programs
  • general: Work-life balance initiatives

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Format & readability score

Tags & Categories

USFDA 510k submissionCE certificationEU MDRISO 13485ISO 1497121 CFR 820Health Canada & CDSCO submissionCAPAHealthcare Technology
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Answer 10 quick questions to check your fit for Regulatory Affairs Manager @ Philips.

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Philips logo

Regulatory Affairs Manager

Philips

Regulatory Affairs Manager

full-timePosted: Jan 13, 2026

Job Description

Job Title

Regulatory Affairs Manager

Job Description

Job title:
Regulatory Affairs Manager

Your role:
• The greater impact of this role. 

This role ensures that Philips’ products comply with global regulatory standards, enabling safe and effective healthcare solutions. This directly impacts patient safety, accelerates product approvals, and supports innovation in medical technology.

• Detail elements of the team and stakeholders for this role. 

You’ll collaborate cross-functionally with Regulatory Affairs Specialists, Quality Assurance, R&D and Engineering, Clinical Affairs, Marketing and Product Management, to ensure compliance throughout the product lifecycle.

• What are the professional and personal opportunities for development within this role?  

Exposure to global regulatory frameworks (FDA, EU MDR, ISO standards), Opportunities for international collaboration and cultural exposure

• From Health and wellness programs to Work-life balance initiatives, a career at Philips comes with all sorts of wonderful benefits. Be sure to speak to your recruiter about benefits in your region. 

You're the right fit if:  
1. Experience: Typically requires 10-15 years of experience in the medical device industry, with a proven track record of successful submissions.
2. Skills: USFDA 510k submission, CE certification, EU MDR, ISO 13485, ISO 14971, 21 CFR 820, Health Canada & CDSCO submission, medical device rules 2017, CAPA
3. Education: Bachelor’s degree in a scientific field (Pharmacy, Biology, or Chemistry) or Engineering; a master’s degree or Regulatory Affairs Certification (RAC) is highly preferred.
4. Anything else: Capacity to manage multiple high-stakes projects simultaneously under strict deadlines.

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

Estimated Salary Rangemedium confidence

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

  • USFDA 510k submissionintermediate
  • CE certificationintermediate
  • EU MDRintermediate
  • ISO 13485intermediate
  • ISO 14971intermediate
  • 21 CFR 820intermediate
  • Health Canada & CDSCO submissionintermediate
  • CAPAintermediate

Required Qualifications

  • 10-15 years experience in medical device industry (experience)
  • Bachelor’s degree in scientific field (Pharmacy, Biology, Chemistry) or Engineering (experience)
  • Master’s degree or RAC preferred (experience)
  • Manage multiple high-stakes projects under deadlines (experience)

Responsibilities

  • Ensure products comply with global regulatory standards
  • Collaborate with QA, R&D, Engineering, Clinical Affairs, Marketing

Benefits

  • general: Health and wellness programs
  • general: Work-life balance initiatives

Target Your Resume for "Regulatory Affairs Manager" , Philips

Get personalized recommendations to optimize your resume specifically for Regulatory Affairs Manager. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Regulatory Affairs Manager" , Philips

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score

Tags & Categories

USFDA 510k submissionCE certificationEU MDRISO 13485ISO 1497121 CFR 820Health Canada & CDSCO submissionCAPAHealthcare Technology
Quiz Challenge

Answer 10 quick questions to check your fit for Regulatory Affairs Manager @ Philips.

10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.