Unilever
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Senior Scientist, Regulatory Affairs
role at
Unilever
4 days ago Be among the first 25 applicants
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About Unilever With 3.4 billion people in over 190 countries using our products every day, Unilever is a business that makes a real impact on the world. Work on brands that are loved and improve the lives of our consumers and the communities around us. We are driven by our purpose: to make sustainable living commonplace, and it is our belief that doing business the right way drives superior performance. At the heart of what we do is our people – we believe that when our people work with purpose, we will create a better business and a better world.
Job Purpose Unilever is the place where you can bring your purpose to life with the work that you do – creating a better business and a better world. If you are inquisitive and a true lover of the personal care industry, then this role is just for you!
Main Responsibilities
Provide regulatory expertise and assessments to R&D project leaders and key business partners across the PC USA product portfolio, aligned with strategic priorities.
Collaborate with the PC North America Regulatory Affairs team to implement regulatory strategies supporting business growth.
Guide R&D through regulatory assessments and formulation reviews for major projects using digital tools.
Manage labeling and artwork activities, including Mastertext discussions and final review of Marketing Masterlock Document (MMLD).
Secure regulatory clearance for clinical, consumer, home-use tests, and sensory studies.
Lead OTC drug expiration date stability programs for regulatory input.
Contribute regulatory input for digital tools development and implementation in R&D.
Work closely with global and local teams to ensure regulatory documentation, safety, and quality compliance.
Collaborate with the Beauty & Wellness Regulatory Team on shared topics.
Qualifications & Experience
BSc in Chemistry, Pharmacy, Biological Science, Toxicology, Environmental Science, or related field.
3-5+ years' experience in FMCG, with expertise in personal care and OTC regulatory requirements.
Knowledge of US federal and state regulations relevant to personal care products.
Experience working with R&D and external partners to support innovation.
Proactive, flexible, results-oriented with strong communication skills.
Ability to influence and develop innovative solutions.
Skills
Proficiency in Microsoft Office; experience with SAP is a plus.
Familiarity with FDA Cosmetics portals and California Safe Cosmetic Program is advantageous.
Leadership & Behaviors
Drive high performance, demonstrate resilience, and collaborate effectively.
Maintain high standards, focus on consumer needs, and exhibit humility and curiosity.
Adhere to standards of leadership like passion, mastery, consumer love, purpose, and agility.
What We Offer Competitive pay, bonus eligibility, long-term incentives, comprehensive benefits including health, retirement, paid leave, and more. We foster a diverse, inclusive environment where all voices matter.
#J-18808-Ljbffr
Senior Scientist, Regulatory Affairs
role at
Unilever
4 days ago Be among the first 25 applicants
Get AI-powered advice on this job and more exclusive features.
About Unilever With 3.4 billion people in over 190 countries using our products every day, Unilever is a business that makes a real impact on the world. Work on brands that are loved and improve the lives of our consumers and the communities around us. We are driven by our purpose: to make sustainable living commonplace, and it is our belief that doing business the right way drives superior performance. At the heart of what we do is our people – we believe that when our people work with purpose, we will create a better business and a better world.
Job Purpose Unilever is the place where you can bring your purpose to life with the work that you do – creating a better business and a better world. If you are inquisitive and a true lover of the personal care industry, then this role is just for you!
Main Responsibilities
Provide regulatory expertise and assessments to R&D project leaders and key business partners across the PC USA product portfolio, aligned with strategic priorities.
Collaborate with the PC North America Regulatory Affairs team to implement regulatory strategies supporting business growth.
Guide R&D through regulatory assessments and formulation reviews for major projects using digital tools.
Manage labeling and artwork activities, including Mastertext discussions and final review of Marketing Masterlock Document (MMLD).
Secure regulatory clearance for clinical, consumer, home-use tests, and sensory studies.
Lead OTC drug expiration date stability programs for regulatory input.
Contribute regulatory input for digital tools development and implementation in R&D.
Work closely with global and local teams to ensure regulatory documentation, safety, and quality compliance.
Collaborate with the Beauty & Wellness Regulatory Team on shared topics.
Qualifications & Experience
BSc in Chemistry, Pharmacy, Biological Science, Toxicology, Environmental Science, or related field.
3-5+ years' experience in FMCG, with expertise in personal care and OTC regulatory requirements.
Knowledge of US federal and state regulations relevant to personal care products.
Experience working with R&D and external partners to support innovation.
Proactive, flexible, results-oriented with strong communication skills.
Ability to influence and develop innovative solutions.
Skills
Proficiency in Microsoft Office; experience with SAP is a plus.
Familiarity with FDA Cosmetics portals and California Safe Cosmetic Program is advantageous.
Leadership & Behaviors
Drive high performance, demonstrate resilience, and collaborate effectively.
Maintain high standards, focus on consumer needs, and exhibit humility and curiosity.
Adhere to standards of leadership like passion, mastery, consumer love, purpose, and agility.
What We Offer Competitive pay, bonus eligibility, long-term incentives, comprehensive benefits including health, retirement, paid leave, and more. We foster a diverse, inclusive environment where all voices matter.
#J-18808-Ljbffr