Sarang Chouhan

Regulatory Affairs Manager at Marc Anthony Cosmetics Ltd.
  • Claim this Profile
Contact Information
us****@****om
(386) 825-5501
Location
Concord, Ontario, Canada, CA

Topline Score

Topline score feature will be out soon.

Bio

Generated by
Topline AI

You need to have a working account to view this content.
You need to have a working account to view this content.

Credentials

  • Regulatory Affairs Certification (RAC)
    Toronto Institute of Pharmaceutical Technology
    Oct, 2017
    - Nov, 2024

Experience

    • Canada
    • Manufacturing
    • 1 - 100 Employee
    • Regulatory Affairs Manager
      • Jan 2020 - Present

      • Successfully filed NHP site license and more than 300 cosmetics notification forms in Canada. • Successfully registered Natural Health Products. (Vitamins, Gummies & Hand Sanitizers) • Implemented Modernization of Cosmetics Regulations Act (MoCRA) FDA, to ensure the compliance with latest regulatory requirements. • Registered over 200 cosmetics products globally, including in Europe and China. • Reviewed 400+ cosmetics labels and NHP monographs for compliance with regulations. • Managed Wercsmart & Smart sorting Retailers registration portal. • Reviewed 300+ formulas for compliance with global and country-specific regulations. • Deeply involved in new product development process for successful product launch. • Managed reformulation projects of non-compliant formulas. • Created a blacklist of ingredients to ensure compliance with retailers and global requirements. • Partnered with the innovation team to research new ingredients. • Reviewed claims of 5 different cosmetics brands' websites to ensure regulatory compliance. • Provided support to the e-commerce team with Amazon queries. • Reviewed Websites of 5 brands to make sure they comply with regulatory standards. • Reviewed and approved press releases and claims published on social media. • Provided solutions to product-related queries from retailers and the sales team. • Able to create product UPCs & SCC codes. • Managed stewardship reporting. • Helped 4 brands get PETA certification. • Experience managing 5 different brands, each with over 100 products simultaneously. • Supervised regulatory team members to manage a database of 5 different brands. • Managed all quality issues related to product formulas and their components. • Managed communication with third-party testing labs, such as HRIPT and claims testing. • Created and updated (SOPs) and GMP forms as required. • Managed communication with contract manufacturers to ensure compliance with regulatory and quality standards. Show less

    • Cosmetics
    • 1 - 100 Employee
    • Regulatory Affairs/Quality Assurance/Quality Control Associate
      • Aug 2017 - Jan 2020

      • Registered Sunscreen (DIN) products and filed Cosmetics notification forms on behalf of customers with Health Canada. • Filed Site Licenses & Product Licenses for Natural health products and Drug products. • Reviewed customer labels for compliance and provided technical writing support for Standard. • Operating Procedures, OOS, CAPA, and NCR investigations. • Proofread technical documentation such as COA, MSDS, Stability Data, and Micro & Preservative reports. • Executed GMP & GLP protocols and gained experience in Health Canada audit. • Maintained good documentation practices and prepared finished good certificates of analysis and QA/QC documents. • Conducted internal audits to ensure quality and regulatory systems are in place and collaborating with internal staff and service providers for regulatory guidance. • Assisted the QA manager during Health Canada Audit by preparing documentation. • Identified quality issues that arise during manufacturing, filing, and packaging and conducted line clearance, finished goods inspection, and in-process inspection for dispensing, manufacturing, filling, and packaging. • Performed testing of raw materials, components, bulk, and finished products for OTC, NHP, and cosmetics, including Specific gravity, Ph, Density, Stability Testing & microbial sampling. • Validated raw material testing and reviewed vendor certificate of analysis to ensure results are within specifications. • Set up and maintained QC product standards and issued QC line standards to production. • Conducted environmental monitoring to evaluate air quality. Show less

Education

  • Toronto Institute of Pharmaceutical Technology
    Regulatory Affairs, Regulatory Affairs Certification
    2016 - 2017
  • Shri G S Institute of Technology & Science
    Bachelor of Pharmacy - B.Pharma, Pharmaceutical Sciences
    2012 - 2016

Community

You need to have a working account to view this content. Click here to join now