Team Member - Manufacturing (Derma)

Dr. Reddy's Laboratories; Andhra Pradesh; On-site; INR 1,200,000 - 1,800,000; Full time

Job summary

Dr. Reddy's Laboratories in Andhra Pradesh is seeking an experienced manufacturing professional to operate production equipment and execute batch manufacturing for dermatology products such as creams, ointments, gels, and lotions.

You will follow BMRs/SOPs, monitor process parameters, and ensure safety, quality, and regulatory compliance throughout operations. Responsibilities include line clearance, record-keeping, participating in investigations, and supporting audits while maintaining audit

Qualifications

• 6–10 years of experience in manufacturing operations.
• Experience in pharmaceutical manufacturing is a plus.
• Knowledge of cGMP, GDP, and QA processes.

Responsibilities

• Follow cGMP and GDP in daily operations.
• Maintain batch records and documentation accurately.
• Support investigations and CAPA implementation.
• Participate in audits and inspection readiness.
• Ensure clean and compliant production areas.

Skills

Lean

Operational Excellence

Kaizen

5S

Education

B.Sc, M.Sc, Diploma - Mechanical Engineering, or related discipline

Job description

Job Description

Role Purpose

To manufacture dermatology products such as creams, ointments, gels, lotions, and topical solutions by operating production equipment, following approved Batch Manufacturing Records (BMRs), complying with cGMP requirements, and ensuring safety, quality, productivity, and regulatory compliance during manufacturing operations.

Key Responsibilities

Manufacturing Operations

• Perform dispensing, sifting, mixing, homogenization, emulsification, and manufacturing activities as per approved BMRs and SOPs.
• Operate manufacturing equipment such as mixers, homogenizers, planetary mixers, manufacturing vessels, transfer pumps, and storage tanks.
• Execute batch manufacturing activities within scheduled timelines.
• Monitor and control process parameters such as temperature, mixing speed, pressure, vacuum, and processing time.
• Carry out batch charging and material addition activities as per manufacturing instructions.
• Perform product transfers between manufacturing vessels and holding tanks.
• Support scale-up and technology transfer batches when required.

Equipment Operation & Maintenance

• Perform equipment preparation, assembly, dismantling, and cleaning activities.
• Conduct pre-operation checks and ensure equipment is fit for use before manufacturing.
• Record equipment usage in logbooks.
• Identify equipment abnormalities and report them to supervisors and engineering teams.
• Support preventive maintenance and equipment qualification activities.

GMP & Documentation

• Complete manufacturing records accurately and contemporaneously.
• Maintain BMRs, equipment logbooks, cleaning records, and area checklists.
• Follow Good Documentation Practices (GDP) at all times.
• Report deviations, incidents, and non-conformances immediately.
• Participate in investigations and CAPA implementation activities.

Quality Compliance

• Ensure adherence to current Good Manufacturing Practices (cGMP).
• Follow approved SOPs, specifications, and manufacturing procedures.
• Perform line clearance verification before and after batch activities.
• Ensure no mix-ups, contamination, or cross-contamination occur during production.
• Support QA during in-process checks and audits.
• Maintain batch traceability throughout manufacturing operations.

Cleaning & Hygiene

• Perform cleaning and sanitization of manufacturing equipment and production areas.
• Follow cleaning validation requirements and cleaning procedures.
• Ensure manufacturing areas are maintained in a clean and inspection-ready condition.
• Dispose of waste materials as per approved procedures.

Safety, Health & Environment

• Follow EHS policies and safe work practices.
• Use required PPE during manufacturing activities.
• Report unsafe conditions, near misses, and safety incidents.
• Participate in safety observations, risk assessments, and emergency response activities.
• Handle chemicals, active ingredients, and cleaning agents safely.

Productivity & Continuous Improvement

• Minimize process losses and material wastage.
• Support Lean, Operational Excellence, and Continuous Improvement initiatives.
• Participate in Kaizen, 5S, and productivity improvement projects.
• Contribute ideas to improve process efficiency, quality, and safety.

Audit & Inspection Readiness

• Maintain production areas in a state of audit readiness.
• Support internal, customer, and regulatory audits.
• Demonstrate process and documentation knowledge during inspections.
• Ensure compliance with USFDA, MHRA, EU GMP, WHO GMP, and other applicable regulatory requirements.

Qualifications

Qualification Requirements

Educational Qualification

Essential

• B.Sc,M.Sc, Diploma - Mechanical Engineering, or related discipline.

6–10 Year

Experience