Director, Medical/Regulatory Writing

Found in: Jooble US O C2 - 3 weeks ago


Los Angeles CA, United States Yoh, A Day & Zimmermann Company Full time

Yoh has an exciting, entry-level opportunity for a Regulatory Affairs Manager to join our client in the Cosmetics Industry out of El Segundo, CA .


If after reviewing, you are interested in learning more about this role please apply with your updated resume ASAP.


Title: Regulatory Affairs Manager
Cosmetics Manufacturing/Consumer Products
Manage and prepare documentation related to a specific formula including preparing IL, SDS, QQ, and coordination of testing (upon customer’s needs).
Verify product compliance with US regulations.
Prepare documents required for export registration upon the customer’s request.
Manage regulatory compliance related to EU PIF/dossiers.
Collect data from vendors on raw materials to support the customer product claims.
Maintain regulatory files for each ingredient (TDS, SDS, Cof A, ingredient breakdown, Impurities profile etc.).
Maintain R&D administrative support role, ingredient compliance with different countries including authorized levels of ingredients in formulas, risk associated with the project.
Provide knowledge of current and future regulations about raw materials, packaging, labeling claims, and other related areas of compliance.
Develop and maintain regulatory standards and protocols to ensure compliance with various international regulations.
Verify product compliance for different countries or areas (when needed): Canada, US, EU, ASEAN countries, UAE.
Establish interaction with regulatory entities (ICMAD etc).
Identify and maintain updated records of complaint raw materials specifications, ability to source and collaborate with RM suppliers to ensure GMP/ISO regulations and standards
Oversee personal care regulatory matters including safety, quality, ingredients, labeling, advertising, source of materials.
Support ISO and CGMP quality systems in coordination with global network of corporate regulatory and quality management.
Keep involved in company’s continuous improvement program of waste minimization within a manufacturing system without sacrificing productivity.

5+ years experience in cosmetic manufacturing
~ Proficiency in Microsoft Excel, Word and Outlook required
~ Must be able to multi-task and handle many on-going projects at a time


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