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Sarita Patade

Mid-level Regulatory Affairs Manager specializing in cosmetics, OTC, and global compliance

Frisco, TXRegulatory Affairs ManagerMid-LevelCosmeticsPersonal Care & BeautyPharmaceuticals
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About

Sourcing/product professional with hands-on experience managing end-to-end contract manufacturing for consumer products (including a pressed eyeshadow palette) from vendor selection and GMP-focused audits through formula approval, pilot batches, claims testing, and launch. Demonstrates strong commercial negotiation (MOQs, tiered pricing, component cost-downs tied to service metrics) and pragmatic risk mitigation, including a COVID-era nutrition drink mix launch pivot to a flavor extension leveraging existing inventory.

Experience

Regulatory Affairs ManagerIthos Global (Cordance Group)
Product Development LeadAtlas World US
Director, New Product LaunchAuraline Beauty
Product Manager, R&DRevital U
Technical Information SpecialistShiseido America Inc
Senior Analytical Lead ScientistShiseido America Inc
Analytical ScientistShiseido America Inc
Analytical ChemistSun Pharma (formerly Able Labs)
Quality ChemistActavis (formerly Amide Pharmaceutical Inc)
Research AssociateIndian Institute of Technology

Education

Mumbai Universitymaster, Organic Chemistry

Key Strengths

  • Owned end-to-end sourcing and launch for a pressed eyeshadow palette (on-time launch, met margin targets)
  • Negotiated flexible MOQs and tiered pricing using multi-vendor proposals and cost breakdowns
  • Reduced costs by sourcing components separately at lower price than manufacturer
  • Built pricing tied to performance/service metrics (defects, shade consistency, on-time production)
  • Thorough CM due diligence (R&D/Quality, GMP, regulatory, equipment, documentation, financials, site audits)
  • Mitigated COVID supply chain risk by pivoting to a flavor extension using existing raw material inventory (6-month execution)
  • Resolved pilot-batch sample delay risk by aligning stakeholders and repurposing lab batch samples for claims testing
  • Improved supplier performance by setting clear documentation expectations, timelines, and recurring check-ins (completed docs for existing SKUs in 3 months)

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Languages

English

Skills

Regulatory affairsRegulatory complianceProduct lifecycle managementProduct registrationRegulatory submissionsRegulatory reportingHealth authority interactionsFDA regulationsFDA 21 CFRFTC complianceDSHEAHealth Canada regulationsEU cosmetic regulationsUK cosmetic regulationsFrench cosmetic regulations