Job Openings
Regulatory Affairs
About the job Regulatory Affairs
Job Title: Regulatory Affairs
Job Location: Kheda, Gujarat, India
Job Location Type: On-site
Job Contract Type: Full-time
Job Seniority Level: Associate
Skills:
Cosmetics, English, Communication, Regulatory Affairs, Regulatory Compliance, Regulatory Requirements,
Responsibilities
Review formulations and claims and provide regulatory guidance to ensure full compliance to regulations including mandatory standards.
Stay abreast with legislation and guidelines that apply to the organizations product portfolio (cosmetics/personal care).
Oversight of the preparation and filing of regulatory documents with the FDA and international regulatory bodies; setting the standards for and reviewing all submissions to assure adequacy and accuracy.
Will scan regulations and mandatory BIS standards and identify opportunities to advocate for revisions in standards towards future fit regulations.
Will scan competition claims for potential challenges or take learnings to guide Unilever innovations.
Thoroughly study EU, USA, Gulf Region and ASEAN cosmetic regulations and help in building advocacy for cosmetic reforms.
Network with other cluster teams and bring regulatory best practices to India.
Artwork approvals for EU, USA, ASEAN, Gulf region scope.
Help drive the Digital RA agenda.
Collaborate closely with business partners to support key business objectives.
Work with cross functional teams and third parties to obtain regulatory documentation for new and existing products related to testing, production, raw materials, formulas, finished goods, supplier documentation and external certifications.
Work closely with third party partners and commercial teams to support international registrations, authorizations and product certifications.
Provide regulatory review of product labels, artwork, manuscripts, information, labels, claims & marketing material to ensure accuracy and compliance.
Update and maintain Product Information Files (PIF), track documentation, and support key regulatory deliverables to support global registration timelines and product launches.
Maintain current knowledge of global cosmetic regulations and chemical compliance through ongoing research and data management.
Compile and organize data for annual reporting requirements and to support product registration requests and cosmetic notification projects.
Support retailer inquiries, technical documentation requests, and general product questions from various communication platforms.
Support internal audits and external certification/audits including Vegan and Cruelty Free.
Qualification & Experience
Education
3+ years of combined regulatory affairs experience in the cosmetics or pharmaceutical industry, both domestically and internationally.
Masters degree in science, with 1-2 years industrial experience or / B. Pharm with at least 4 years of industrial experience in Regulatory Affairs or Cosmetics skin care, hair care, color cosmetics.
Cosmetics, English, Communication, Regulatory Affairs, Regulatory Compliance, Regulatory Requirements,
Responsibilities
Review formulations and claims and provide regulatory guidance to ensure full compliance to regulations including mandatory standards.
Stay abreast with legislation and guidelines that apply to the organizations product portfolio (cosmetics/personal care).
Oversight of the preparation and filing of regulatory documents with the FDA and international regulatory bodies; setting the standards for and reviewing all submissions to assure adequacy and accuracy.
Will scan regulations and mandatory BIS standards and identify opportunities to advocate for revisions in standards towards future fit regulations.
Will scan competition claims for potential challenges or take learnings to guide Unilever innovations.
Thoroughly study EU, USA, Gulf Region and ASEAN cosmetic regulations and help in building advocacy for cosmetic reforms.
Network with other cluster teams and bring regulatory best practices to India.
Artwork approvals for EU, USA, ASEAN, Gulf region scope.
Help drive the Digital RA agenda.
Collaborate closely with business partners to support key business objectives.
Work with cross functional teams and third parties to obtain regulatory documentation for new and existing products related to testing, production, raw materials, formulas, finished goods, supplier documentation and external certifications.
Work closely with third party partners and commercial teams to support international registrations, authorizations and product certifications.
Provide regulatory review of product labels, artwork, manuscripts, information, labels, claims & marketing material to ensure accuracy and compliance.
Update and maintain Product Information Files (PIF), track documentation, and support key regulatory deliverables to support global registration timelines and product launches.
Maintain current knowledge of global cosmetic regulations and chemical compliance through ongoing research and data management.
Compile and organize data for annual reporting requirements and to support product registration requests and cosmetic notification projects.
Support retailer inquiries, technical documentation requests, and general product questions from various communication platforms.
Support internal audits and external certification/audits including Vegan and Cruelty Free.
Qualification & Experience
Education
3+ years of combined regulatory affairs experience in the cosmetics or pharmaceutical industry, both domestically and internationally.
Masters degree in science, with 1-2 years industrial experience or / B. Pharm with at least 4 years of industrial experience in Regulatory Affairs or Cosmetics skin care, hair care, color cosmetics.
Lifelancer ( https://lifelancer.com ) is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains.
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