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Senior Executive Quality Assurance
4 weeks ago
All products are manufactured through qualified third-party (3 P) partners; world-class quality is mission-critical.
Role Mission Own end-to-end product quality across our 3 P manufacturing network.
Build and enforce gold-standard QA systems so every MARS batch is safe, compliant, high-performing, and consumer-delighting.
Key Outcomes (First 12 Months)
• Implement standardized QA agreements & GMP audit scorecards across 100% of 3 P sites.
• Reduce batch release cycle time to 95% on-spec batch acceptance rate (rolling 6 months).
Core Responsibilities
• 3 P Quality Governance – Draft, negotiate, and enforce quality & technical agreements; maintain approved vendor list.
• GMP Audits & Compliance – Plan and conduct risk-based onsite audits (≥2/site/year); issue NC reports; drive CAPA closure.
• Batch Release Control – Review COAs, in-process data, micro results, stability & packaging compatibility; authorize release/hold.
• Specifications & Change Control – Maintain master product & packaging specs; manage deviations, reworks, relabeling approvals.
• Regulatory Readiness – Ensure BIS registration, CDSCO compliance, labeling/claims checks; align with ISO 22716 & relevant global cosmetic regs.
• Complaint & Deviation Management – Lead root-cause analysis (5-Why, Fishbone); trend recurring issues; feed prevention actions to R& D & Procurement.
• Supplier / Material Qualification – Support onboarding of new formulas, actives, pigments, and packaging; conduct first-article & incoming QA checks.
• Stability & Shelf-Life – Coordinate accelerated/real-time studies; track results against claims and storage conditions.
• Documentation & QMS – Own SOPs, forms, logs, electronic records (ERP/LIMS); ensure data integrity & audit trails.
• Cross-Functional Support – Partner with R& D, Packaging Dev, Ops, and Logistics on scale-ups, artwork, line trials, and recall readiness.
Must-Have Qualifications
• B.
Pharm / B.
Tech (Cosmetic Tech, Chemical Engg, Pharmacy, or related).
• 5–8 years QA/QC experience in cosmetics, personal care, or FMCG with multi-site 3 P / contract manufacturing exposure.
• Working knowledge of ISO 22716 (Cosmetic GMP), BIS standards, stability & microbiological testing.
• Strong documentation discipline; proficient with MS Office / Google Sheets; exposure to ERP / LIMS / e QMS tools.
• Hands-on auditor comfortable in plants, labs, and with suppliers; willing to travel ~25%.
Soft Skills That Matter
• High ownership & follow-through in a fast, entrepreneurial environment.
• Clear written documentation; confident cross-functional communicator.
• Ability to negotiate quality expectations with external partners without damaging relationships.
• Analytical mindset; comfortable with numbers, risk scoring, and prioritization.