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Puig

Regulatory Affairs Specialist – Home Care, Chemical Compliance

Puig

. Perform regulatory compliance assessments for Home Care products and related categories.

Posted 10/23/2026contractBarcelona • SpainJuniorWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in regulatory compliance assessments and guidance for Home Care products, with a strong focus on global chemical and cosmetic regulations. Proficient in managing regulatory documentation and ensuring adherence to applicable standards while contributing to process improvements.

Highest-signal resume keywords
Regulatory Compliance AssessmentsKnowledge of CLP RegulationsSafety Data Sheets (SDS) GenerationRegulatory Documentation ManagementAdvanced Microsoft Excel Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Regulatory Compliance AssessmentsKnowledge of CLP RegulationsSafety Data Sheets (SDS) GenerationRegulatory Documentation ManagementChemical Labeling ComplianceHazard ClassificationRegulatory Process ImprovementInternational Market AccessKnowledge of K-REACHKnowledge of AICIS
Soft Skills
Analytical SkillsProblem-Solving SkillsOrganizational SkillsAttention to DetailFlexibility
Tools & Technologies
Microsoft OfficeExcelExESSSAP
Industry Keywords
Regulatory AffairsChemical IndustryCosmetic IndustryGlobal RegulationsIngredient Compliance

About the role

Key responsibilities & impact
  • Perform regulatory compliance assessments for Home Care products and related categories.
  • Provide regulatory guidance to cross-functional teams during product development and approval processes.
  • Assess packaging constraints and labelling feasibility, and review and approve product artworks to ensure regulatory compliance.
  • Ensure technical documentation and regulatory processes comply with applicable global regulations and internal standards.
  • Conduct hazard classification in accordance with CLP and other applicable chemical regulations.
  • Generate, review and approve Safety Data Sheets (SDS) where required.
  • Create, review and approve chemical product labels in compliance with applicable regulatory requirements.
  • Manage regulatory documentation and substance inventories required for international market access and export compliance.
  • Monitor regulatory developments and assess their impact on products, ingredients and business processes.
  • Contribute to regulatory process improvement and digitalisation initiatives.

Requirements

What you’ll need
  • Minimum 1 to 2 years of experience in Regulatory Affairs within the chemical and/or cosmetic industry.
  • Knowledge of Regulation (EC) No. 1272/2008 on Classification, Labelling and Packaging (CLP) of substances and mixtures.
  • Knowledge of global cosmetic regulations and ingredient compliance requirements would be an asset.
  • Knowledge of international chemical regulations such as K-REACH (Korea), CSCL (Japan), DSL/NDSL (Canada) and AICIS (Australia) would be considered a strong advantage.
  • Master's degree in Chemistry, Pharmacy, Toxicology, Biology or another relevant scientific disciplines.
  • Spanish.
  • English.
  • Strong analytical, problem-solving and organizational skills with a high level of attention to detail.
  • Ability to meet deadlines while being flexible to changes in priorities and interruptions.
  • Ability to manage multiple priorities and deliver high-quality results in a fast-paced environment.
  • Advanced user of Microsoft Office applications, particularly Excel.
  • ExESS knowledge is a valuable plus.
  • SAP knowledge is a plus.

Benefits

Comp & perks
  • An entrepreneurial, creative and welcoming work culture
  • A range of learning and development opportunities
  • An international company with plenty of opportunities to grow
  • A competitive compensation & benefits package