Executive - Quality Assurance (Vasai)

Foxtale; Vasai; Presencial; INR 500.000 - 750.000; Jornada completa

Descripción de la vacante

Foxtale in Vasai, Maharashtra is seeking an Executive - Quality Assurance to support day-to-day QA/QC across internal and contract manufacturing operations. You will perform routine shop-floor quality checks, review batch records, and assist in investigations to ensure compliance with cGMP and brand safety standards.

The ideal candidate has a B.Pharm or related degree, 3-5 years hands-on QA/QC experience in cosmetics or pharmaceutical manufacturing, and strong knowledge of ISO 22716 and batch

Formación

• Ideal candidate holds a B.Pharm or related science degree with hands‑on QA/QC exposure.
• Strong understanding of cosmetic cGMP (ISO 22716) and FDA basics.
• Experience reviewing Batch Manufacturing Records and Certificates of Analysis.

Responsabilidades

• Perform line clearances, sample collection, and daily quality inspections on site.
• Review BMR, BPR, and COA to ensure release specifications are met.
• Log complaints, document deviations, and assist in RCA and CAPA activities.
• Monitor GMP adherence and SOPs across production lines and warehouses.
• Support internal/vendor audits and routine stability testing sample pullouts.

Conocimientos

Attention to detail

Execution focus

Educación

B.Pharm

Chemistry

Biotechnology

Descripción del empleo

Designation: Executive - Quality Assurance

Location: Vasai, Maharashtra

Employment Type: Full-time

Job Summary

The Executive - Quality Assurance will support day-to-day Quality Assurance and Quality Control (QA/QC) execution across internal and contract manufacturing operations. In this role, you will perform routine shop-floor quality checks, review batch records, support complaint investigations, and ensure that all production runs meet cGMP and brand safety standards.

Key Responsibilities

• Routine QA/QC Execution: Perform line clearances, sample collections, and daily quality inspections at manufacturing and packaging sites.
• Batch Record Review: Review Batch Manufacturing Records (BMR), Batch Packaging Records (BPR), and Certificates of Analysis (COA) to ensure specifications are met before product release.
• Deviations & Complaints Support: Log customer complaints, document quality deviations, and assist in conducting Root Cause Analysis (RCA) and Corrective & Preventive Actions (CAPA).
• GMP Compliance: Monitor daily adherence to ISO 22716 (Cosmetic GMP) guidelines and internal quality SOPs across production lines and warehouses.
• Audit & Stability Assistance: Support internal and vendor quality audits, maintain quality documentation archives, and assist with routine stability testing sample pullouts.

Ideal Candidate Background

• Education: Bachelors degree in Pharmacy (B.Pharm), Chemistry, Biotechnology, or a related scientific field.
• Experience: 3-5 years of hands-on QA/QC experience in cosmetics, skincare, personal care, or pharmaceutical manufacturing setups.
• Technical Familiarity: Good working knowledge of Cosmetic cGMP (ISO 22716), basic FDA requirements, and batch documentation review.

What We're Looking For

• Attention to Detail: Meticulous eye for numbers, batch logs, and physical product inspections.
• Execution Focus: Strong willingness to work on the shop floor, follow SOPs, and maintain accurate records under tight operational timelines.

Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.