Senior Production Chemist

PS Human Resources And Consultants; Raigad; On-site; INR 800,000 - 1,200,000; Full time

Job summary

PS Human Resources And Consultants is seeking a Senior Production Chemist in Maharashtra to plan, supervise, and execute manufacturing activities with focus on safety, quality, and regulatory compliance. The role includes manpower supervision, production planning, documentation, equipment use, and continuous process improvement.

Responsibilities include ensuring dialysis and biomedical product manufacturing per approved Batch, monitoring process parameters, and coordinating with QA/QC for batch

Qualifications

• B.Sc./M.Sc. in Chemistry or related field required.
• 5–6 years QC experience in pharmaceutical manufacturing.
• Experience with cGMP, ISO 13485 (where applicable), MDR 2017.

Responsibilities

• Plan, supervise, and execute daily production activities as per the approved production schedule.
• Ensure manufacturing of dialysis solutions and biomedical products per Batch.
• Monitor critical process parameters for quality and consistency.
• Optimize manpower, machinery, and resources usage.
• Review Batch Manufacturing Records and Batch Packing Records.
• Document all production activities accurately.
• Coordinate with QA/QC for in-process checks and batch release.
• Supervise Production Chemists, Operators, and Assistants.
• Train personnel on GMP, SOPs, safety, and operations.
• Support audits and ensure EHS compliance.
• Maintain cleanroom discipline and housekeeping standards.

Skills

GMP Awareness

SOP Adherence

QA Oversight

Education

B.Sc./M.Sc. in Chemistry

Job description

Job Summary

The Senior Production Chemist is responsible for planning, supervising, and executing manufacturing activities to ensure products are produced safely, efficiently, and in compliance with cGMP, ISO 13485 (where applicable), Medical Device Rules (MDR) 2017, approved procedures, and company quality standards. The role includes manpower supervision, production planning, documentation, equipment utilization, and continuous process improvement

Role & responsibilities

Plan, supervise, and execute daily production activities as per the approved production schedule.

• Ensure manufacturing of dialysis solutions and biomedical products in accordance with approved Batch
• Monitor critical process parameters to ensure product quality and process consistency.
• Ensure optimum utilization of manpower, machinery, and production resources.
• Review and verify Batch Manufacturing Records (BMR) and Batch Packing Records (BPR).
• Ensure accurate documentation of all production activities.
• Monitor dispensing, mixing, filtration, filling, sealing, sterilization, and packaging processes.
• Investigate and document deviations, incidents, and non-conformances.
• Ensure compliance with GMP, GLP, ISO 13485, WHO-GMP, and company quality standards.
• Maintain strict adherence to SOPs and safety procedures.
• Coordinate with Quality Assurance (QA) and Quality Control (QC) for in-process checks and batch release activities.
• Participate in internal and external audits.
• Supervise Production Chemists, Operators, and Production Assistants.
• Allocate work and monitor employee productivity.
• Train production personnel on GMP, SOPs, safety, and operational procedures.
• Promote teamwork and continuous improvement.
• Coordinate with Stores for timely availability of raw materials and packing materials.
• Monitor material consumption and minimize wastage.
• Ensure proper storage and handling of production materials.
• Ensure compliance with EHS (Environment, Health & Safety) policies.
• Maintain cleanroom discipline and housekeeping standards.
• Promote safe working practices and use of PPE.

Preferred candidate profile

Qualification

- B.Sc./M.Sc. in Chemistry, Analytical Chemistry, Pharmaceutical Chemistry, or a related science discipline.

Experience

: 5-6 years of Quality Control experience in pharmaceutical manufacturing.