Production Chemist

PS Human Resources And Consultants; Raigad; On-site; INR 900,000 - 1,200,000; Full time

Job summary

PS Human Resources And Consultants invites applications for a Senior Production Chemist to plan, supervise, and execute manufacturing of dialysis solutions and biomedical products ensuring safety, efficiency, and regulatory compliance.

You will monitor production processes (mixing, filtration, filling, sterilization, packaging), review BMR/BPR, investigate deviations, train staff, and coordinate with QA/QC for batch release and material availability. On-site in Raigad district, Maharashtra.

Qualifications

• Bachelor's or Master's in Chemistry or related field.
• 5–6 years of pharma/biomedical manufacturing experience.
• Strong knowledge of cGMP, ISO 13485 and related quality standards.

Responsibilities

• Plan and supervise daily production per approved schedules and procedures.
• Monitor processes: mixing, filtration, filling, sealing, sterilization, packaging.
• Ensure compliance with cGMP, ISO 13485, MDR 2017 and SOPs.
• Review BMR and BPR and investigate deviations/non-conformances.
• Coordinate with QA/QC and Stores for batch release and material availability.
• Supervise and train production chemists and operators.
• Optimize manpower, machinery, material utilization and minimize waste.
• Maintain EHS, cleanroom, housekeeping, PPE and safety standards.

Skills

Biomedical Manufacturing

Dialysis Solutions

IV Fluids

Sterile Manufacturing

Medical Devices

GMP & ISO Compliance

Production Documentation

Team Supervision

Education

B.Sc./M.Sc. in Chemistry

Job description

Role & responsibilities

Job Summary

The Senior Production Chemist will plan, supervise, and execute manufacturing activities to ensure safe, efficient, and compliant production of dialysis solutions and biomedical products.

Key Responsibilities

• Plan and supervise daily production as per approved schedules and procedures.
• Monitor critical production processes, including mixing, filtration, filling, sealing, sterilization, and packaging.
• Ensure compliance with cGMP, ISO 13485, MDR 2017, SOPs, and quality standards.
• Review Batch Manufacturing Records (BMR) and Batch Packing Records (BPR).
• Investigate deviations, incidents, and non-conformances and maintain accurate documentation.
• Coordinate with QA, QC, and Stores for in-process checks, batch release, and material availability.
• Supervise and train Production Chemists, Operators, and Production Assistants.
• Optimize manpower, machinery, material utilization, and minimize production wastage.
• Maintain EHS, cleanroom, housekeeping, PPE, and safety standards.
• Participate in audits and drive continuous process improvement.

Qualification & Experience

• Education: B.Sc./M.Sc. in Chemistry, Analytical Chemistry, Pharmaceutical Chemistry, or related discipline.
• Experience: 56 years in pharmaceutical, sterile, biomedical, IV fluid, or medical device manufacturing.

Key Skills

Biomedical Manufacturing | Dialysis Solutions | IV Fluids | Sterile Manufacturing | Medical Devices | GMP & ISO Compliance | Production Documentation | Team Supervision