Dr. Reddy’s Laboratories: Team Member Packing (CAM Auto cartonator HV1 ) — Baddi, India

Dr. Reddy’s Laboratories lists a Team Member Packing (CAM Auto cartonator HV1 ) opening in Baddi, India. The position is listed as full-time. The job description covers Lean, maintenance, GMP, audit, compliance, training, root-cause analysis.

Recruitment overview

OrganisationDr. Reddy’s Laboratories
Post / roleTeam Member Packing (CAM Auto cartonator HV1 )
Employment typeFull-time
Notification / job IDREF26198O
Job locationBaddi, India
Work arrangementOn-site
Educational qualificationDegree / qualification: Educational qualificatio n: Diploma in Pharmaceutical Sciences, Pharmacy, Industrial Engineering or a related field is mandatory
Experience required2+ / 4+ years of experience
Salary / stipendSee employer notice for pay details
Last date to applySee official notice

About Dr. Reddy’s Laboratories

Dr. Reddy’s Laboratories is a pharmaceutical business with research and development, medicine-manufacturing and commercial activities. Its employer description centres on making affordable and innovative medicines accessible. The organisation connects scientific development with the production and delivery of pharmaceutical products, rather than operating only as a research laboratory. Its published business priorities include strengthening existing medicine activities, developing future opportunities and conducting operations with attention to people, resources and corporate governance.

The position and its setting

Dr. Reddy’s Laboratories lists Team Member Packing (CAM Auto cartonator HV1 ) in Baddi, India, under reference REF26198O. The details below separate the work described by the employer from essential conditions, preferred experience and practical preparation advice.

  • Employment type: Full-time
  • Employer listing date: 23 October 2026
  • Job Family: Manufacturing
  • Brands: Dr Reddy's Laboratories Limited

Responsibilities and work described

  • Job Summary
  • This role is for a packing operations associate responsible for setting up and operating packing line machinery, ensuring compliance with GMP, GDP, and safety standards
  • The position involves performing line clearance, managing changeovers, recording batch activities, and maintaining equipment through CLTI and preventive maintenance
  • Contribution: to regulatory readiness by maintaining accurate documentation, supporting RCA and CAPA during breakdowns, and cooperating during audits
  • The role emphasizes adherence to SOPs, personal safety practices, and continuous improvement through Kaizen, 5S, and lean initiatives
  • Additionally, you will engage in training programs, safety drills, and digital system usage (SOR, OEE dashboards) to strengthen operational efficiency and compliance
  • Be responsible for setting up and operating packing line machinery, loading materials, and ensuring efficient operations
  • Be responsible for performing line clearance, managing changeovers, and ensuring correct product labeling with batch and regulatory information
  • Be responsible for recording all activities in compliance with GMP, maintaining documentation, and supporting audits
  • Be responsible for cleaning and sanitizing packing lines, performing CLTI activities, verifying calibration, and troubleshooting minor equipment issues
  • Be responsible for reporting equipment issues, supporting preventive maintenance, and implementing CAPA for repeat issues
  • Be responsible for consistently following PPE, hygiene, and safety standards, reporting incidents, and executing LOTO procedures
  • Be responsible for participating in training sessions, safety drills, SOP updates, and engaging in Kaizen, 5S, and lean initiatives
  • Be responsible for using computerized systems (SOR), digital dashboards (OEE, Plant Visibility, AMPLE), and supporting root cause analysis to improve efficiency

Essential requirements and candidate background

  • Educational qualificatio n: Diploma in Pharmaceutical Sciences, Pharmacy, Industrial Engineering or a related field is mandatory
  • Minimum work
  • 2+ / 4+ years of experience
  • Skills & attributes &Critical exposures
  • Functional Skills
  • Equipment Maintenance
  • Incident Reporting
  • Material Handling
  • Packaging Machine Operation
  • Pharmaceutical Packaging
  • Regulatory Compliance
  • Resident Skills
  • Current Good Manufacturing Practices (cGMPS)
  • Digital Literacy
  • Good Documentation Practices
  • Safety Standards
  • Lean Methodologies
  • Behavioural Skills
  • Safety-first mindset with compliance and regulatory alignment
  • Collaborative across cross-functional teams and external stakeholders

Preferred experience and additional strengths

  • Exposure: troubleshooting, assisting in the qualification and calibration of packing equipment, and understanding overall equipment efficiency (OEE) is preferred
  • Exposure: basic safety knowledge (EHS) related to moving machinery risks and compliance with Safety Standards standards is preferred

Location, schedule and contract conditions

  • Work arrangement: On-site
  • Advertised location: Baddi, India

Pay and application dates

A verified salary figure is not established in this article. An online estimate for another Team Member Packing (CAM Auto cartonator HV1 ) vacancy is not an offer for reference REF26198O; use the employer’s own pay disclosure and recruitment communication.

A closing date is not confirmed in this article. Check the current employer page before submitting: an undated posting can change or be withdrawn.

How to apply to Dr. Reddy’s Laboratories

Applications follow the official employer page linked below.

Open the official Dr. Reddy’s Laboratories posting below and match the title and reference REF26198O.

Compare your qualifications and experience with the essential conditions for the Baddi, India position, then read the preferred criteria separately.

Prepare an accurate CV and the supporting items requested in that employer’s application. Provide only information and documents you are authorised to share.

Use the employer’s application option, complete the required fields and review the submission. Retain the acknowledgement when one is provided. Job Alerts World does not receive the application.

Practical preparation: GMP

GMP references concern work performed within a controlled manufacturing or quality environment. In an application, explain your actual involvement with procedures, records, deviations or other controls relevant to the post.

Relevant skills

  • GMP
  • Lean
  • maintenance
  • audit
  • compliance
  • training
  • root-cause analysis
  • problem resolution
  • manufacturing
  • pharmacy

Important links

Official notification / job descriptionOpen official page
Online application portalOpen official page

Read the complete official notice before applying. Availability and requirements can change.

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