Job Overview

We are seeking an experienced QA Chemist to support production quality, manufacturing readiness, and factory capacity. This role will serve as a key technical approval authority for production release, ensuring products are manufactured consistently

Key Responsibilities

- Review factory production capacity, manufacturing schedules, and timelines to minimize production delays.
- Monitor production plans to ensure complete quantities are manufactured according to approved orders.
- Identify material or component shortages and ensure appropriate quantities are available for uninterrupted production.
- Confirm timely availability of components and third-party filling or manufacturing services.
- Review and approve master manufacturing instructions, batch manufacturing records, filling specifications, and final pack-out requirements.
- Verify formulas, batch sizes, filling tolerances, assembly procedures, coding requirements, and inspection standards before production.
- Review pilot batches, scale-up production, line trials, and process validation activities.
- Monitor in-process quality controls, including filling accuracy, torque, sealing, crimping, capping, coding, assembly, and finished-product appearance.
- Review and investigate production deviations, non-conformances, OOS results, and quality-related manufacturing issues.
- Evaluate and support CAPA implementation and follow-up activities.
- Approve, reject, quarantine, or require rework of finished production based on established quality requirements.
- Confirm availability of bulk formula, packaging components, equipment, labour, production capacity, and approved documentation before manufacturing starts.
- Track actual production output against planned capacity and production schedules.
- Analyze yield, scrap, setup losses, rework, material shortages, damaged components, and overall production efficiency.




- Maintain records of components damaged during filling or assembly and support documentation for factory chargebacks with Production Finance.
- Identify and escalate quality, capacity, material, or manufacturing risks that could impact production schedules or customer deliveries.
- Maintain accurate technical documentation and communicate production quality decisions clearly with contract manufacturers and internal stakeholders.

Required Skills

- Strong knowledge of GMP, production quality systems, and manufacturing controls.
- Practical understanding of bulk manufacturing, filling, assembly, and finished-product release.
- Ability to review and interpret batch records, manufacturing instructions, specifications, and production documentation.
- Robust knowledge of in-process testing and production quality inspection.
- Experience investigating deviations, non-conformances, OOS results, and implementing CAPA.
- Hands-on experience with production quality, bulk manufacturing, filling, assembly, batch documentation, in-process testing, and finished-product release.
- Demonstrated experience working with GMP requirements, quality investigations, deviations, CAPA, process validation, and manufacturing controls.
- Experience supporting production planning, factory capacity assessment, and manufacturing readiness.
- This position requires travel to South Korea for factory inspections about 6 times a year.
- You must have a valid passport and meet visa requirements

Pay: ₹300,000.00 - ₹500,000.00 per year

Application Question(s):

- Are you an immediate joiner
- What is your highest level of education, and in which field did you study?
- Describe your experience in cosmetic, personal care manufacturing
- What is your experience with batch manufacturing records and production documentation.
- Describe your experience with GMP, CAPA, and quality management systems.
- What was your last verifiable monthly salary and expected salary
- Do you have valid passport and ready to travel occasionally as per business requirements

Work Location: Remote

📌 Quality Assurance Chemist (India)
🏢 Creations Craft
📍 India