JOB DETAILS
Team Member - Manufacturing (Derma)
CompanyDr Reddy's Laboratories Limited
LocationIndia
Work ModeOn Site
PostedSeptember 15, 2026
About The Company
Established in 1984, we are a global pharmaceutical company headquartered in Hyderabad, India. Driven by our purpose of ‘Good Health Can’t Wait’, we work to provide access to affordable and innovative medicines. We offer a portfolio of products and services including APIs, generics, branded generics, biosimilars and OTC. Our major markets include USA, India, Russia & CIS countries, China, Brazil and Europe. As a company with a history of deep science that has led to several industry firsts, we continue to plan ahead and invest in future growth drivers such as access to novel molecules, digital therapeutics and consumer healthcare. As an early adopter of sustainability and ESG actions, we released our first Sustainability Report in 2004. Our current ESG goals aim to set the bar high in environmental stewardship; access and affordability for patients; diversity; and governance. For more information, log on to: www.drreddys.com.
Caution Notice: Dr. Reddy's has been made aware of candidates receiving fraudulent job opportunities from unauthorised recruiting agencies or people impersonating Dr. Reddy's leaders. These fraudulent jobs may be advertised on employment sites or mimic our careers site and company email addresses. Please know that Dr. Reddy's Laboratories has no affiliation or connection to these situations. Dr. Reddy's (and its associated/group companies) follows a formal recruitment process through its own HR department. Please report immediately in case you suspect a fraudulent job. You may raise your concern by:
Accessing https://drreddys.ethicspoint.com.
Calling on the hotline number. List of hotline numbers are available in https://drreddys.ethicspoint.com. The hotline is available 24x7 in multiple languages.
Writing to complianceofficer@drreddys.com or chiefombudsperson@drreddys.com.
For our community guidelines on LinkedIn, please visit: https://shorturl.at/LTvNZ
About the Role
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.
Experience
6–10 Year
Key Skills
Manufacturing operationscGMP complianceBatch manufacturing recordsEquipment operationHomogenizationEmulsificationQuality controlDocumentation practicesProcess monitoringEquipment maintenanceSafety protocolsLean manufacturingAudit readinessRegulatory complianceWaste managementLine clearance
Categories
ManufacturingScience & ResearchEngineeringSecurity & Safety
Job Information
📋Core Responsibilities
The team member is responsible for manufacturing dermatology products by operating production equipment and following approved Batch Manufacturing Records. They must ensure compliance with cGMP standards, maintain equipment, and support quality audits throughout the production process.
📋Job Type
full time
📊Experience Level
5-10
💼Company Size
32976
📊Visa Sponsorship
No
💼Language
English
🏢Working Hours
40 hours
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