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Regulatory affairs specialist

Page Personnel
Publicada el Publicado hace 21 hr horas
Descripción

Raw Material Assessment

Perform risk assessments of raw materials to ensure compliance with applicable regulatory frameworks (e.g., REACH, CLP, cosmetic regulations).

Liaise with suppliers to collect and verify technical documentation (INCI lists, Safety Data Sheets, IFRA certificates, etc.).

Manage the homologation process for new raw materials, ensuring traceability and regulatory alignment.


Regulatory Data Management

Gather, organize, and maintain regulatory data related to raw materials and finished products.

Ensure accuracy and completeness of documentation in internal databases and regulatory systems.

Prepare and support documentation for audits, product registrations, and regulatory submissions.


Process Optimization

Identify opportunities to streamline regulatory workflows, including change control and documentation processes.

Collaborate with cross‑functional teams (R&D, Quality, Purchasing, Production) to facilitate timely approvals and product launches.

Implement digital tools and automation to improve efficiency and reduce manual workload.


Qualifications

Bachelor's degree in Regulatory Affairs, Life Sciences, Chemistry, Pharmacy, Chemical Engineering, or a related field.

Additional training or certification in regulatory affairs is a plus.


Experience & Skills

* Solid experience in regulatory environments related to cosmetics or chemical raw materials.
* In‑depth knowledge of global regulatory frameworks (EU, FDA, ASEAN, LATAM, etc.).
* Strong analytical and data management skills.
* Advanced proficiency in Excel; experience with SAP is a plus.
* High attention to detail and accuracy.
* Excellent communication skills, adaptability, and persistence.
* Ability to work independently and collaboratively in a team‑oriented environment.


Languages

* Spanish: Fluent
* English: Fluent
* French: a plus
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