Regulatory Affairs Specialist (Barcelona)

Regulatory Affairs Specialist (Barcelona)

24 oct
|
Puig
|
Barcelona

24 oct

Puig

Barcelona

The Opportunity

Reporting to the Regulatory Affairs Manager and as part of the Safety and Regulatory Affairs Department, the role holder will be responsible for ensuring compliance with applicable chemical regulations and internal policies for the global Home Care portfolio, and to provide regulatory support on product development, ingredient compliance, hazard classification, labelling, safety documentation, and market access requirements.

What you'll get to do

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 integral 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

We'd love to meet you if you have

Experience:

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.

Education:

Master's degree in Chemistry, Pharmacy, Toxicology, Biology or another relevant scientific disciplines. Nice to have: training in REACH Regulation, CLP Regulation, and Safety Data Sheets (SDS)

Languages:

Spanish English

Competencies:

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.

Specific Knowledge required:

Advanced user of Microsoft Office applications, particularly Excel. ExESS knowledge is a valuable plus. SAP knowledge is a plus.

We welcome Creators Of All Kinds. If you are unsure of meeting all the requirements but trust you have the transferable skills to excel in this role, complete the application and our teams will get in touch if you are selected for an interview.

What you'll love about us

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

📌 Regulatory Affairs Specialist (Barcelona)
🏢 Puig
📍 Barcelona

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