Dr. Reddy’s Laboratories: Team Member - Manufacturing (Peptide) — Pydibimavaram, AP, India

Dr. Reddy’s Laboratories lists a Team Member - Manufacturing (Peptide) opening in Pydibimavaram, AP, India. The position is listed as full-time. The job description covers quality control, quality assurance, manufacturing, maintenance, compliance, warehouse operations.

Recruitment overview

OrganisationDr. Reddy’s Laboratories
Post / roleTeam Member - Manufacturing (Peptide)
Employment typeFull-time
Notification / job IDREF24946S
Job locationPydibimavaram, AP, India
Work arrangementOn-site
Educational qualificationDegree / qualification: Educational qualification: An B.Sc/ M.Sc (Analytical/ Organic Chemistry)
Experience requiredMinimum work experience: 3 to 5 years 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 - Manufacturing (Peptide) in Pydibimavaram, AP, India, under reference REF24946S. 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: 21 October 2026
  • Job Family: Manufacturing
  • Brands: Dr Reddy's Laboratories Limited

Responsibilities and work described

  • Job Summary
  • An individual to ensure strict adherence to safety protocols, SOPs, and quality standards, ensuring batch manufacturing activities, coordinating with various departments to maintain operational efficiency
  • The role involves executing production activities, coordinating with cross-functional teams and meeting production targets
  • Be responsible for adherence to company safety norms, policies, and SOPs (Standard Operating Procedures)
  • Execute batch manufacturing activities according to e-BMR instructions and workflow, ensuring submission of executed e-BMR and workflows to IPQA (In-Process Quality Assurance) department
  • With support of the MSAT and IPDO team execute trial, validation and commercial batches
  • Your role involves coordination with other departments such as warehouse, QC (Quality Control) and others
  • Be accountable for timely completion of calibration, preventive maintenance activities, and reducing production breakdown time through coordination with shift in-charge and engineering department
  • Initiate quality notification, breakdown notification
  • Involve in commissioning and qualification activities of the equipment
  • Quality / delivery: qualification, validation, calibration of equipment, and process validation are done as per schedule and requirements
  • Quality / delivery: clean room practices are followed as per the SOP and maintain as per the desired conditions
  • Be responsible for maintaining overall operating area to meet current regulatory compliance and norms

Essential requirements and candidate background

  • Educational qualification: An B
  • Sc/ M
  • Sc (Analytical/ Organic Chemistry)
  • Minimum work experience: 3 to 5 years Experience
  • Skills & attributes:
  • Operation of critical equipment like reverse phase chromatography, Micro-wave reactor, Lyophilizer
  • Ensuring the OEE of the equipment and utilization
  • Proficiency: utilizing MES software to execute batch manufacturing activities and ensure compliance with e-BMR instructions
  • Understanding: Quality Management Systems, including SOPs, URS and protocols, to ensure adherence to quality standards
  • Familiarity: SAP software for initiating quality notifications, breakdown notifications
  • Knowledge: Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP) to ensure compliance with regulatory requirements and quality standards
  • Experience: executing the qualification, validation, and calibration of equipment, as well as process validation activities, ensuring adherence to schedule and regulatory requirements
  • Behavioural skills
  • Keen leaner and implement what has been learnt and ensuring adherence to safety norms and quality standards
  • Effective communication skills to communicate with various departments, ensuring seamless collaboration and alignment of activities
  • Capacity to identify and address production-related issues promptly
  • Ensure timely completion of calibration, preventive maintenance and other operational activities
  • Commitment to maintaining current regulatory compliance and adherence to norms to uphold product quality and safety standards

Location, schedule and contract conditions

  • Work arrangement: On-site
  • Advertised location: Pydibimavaram, AP, India

Benefits mentioned by the employer

  • At Dr
  • Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs
  • The benefits you will enjoy at Dr
  • Reddy’s are on par with the best industry standards
  • They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself
  • Our Work Culture
  • Ask any employee at Dr
  • Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait
  • This is our credo as well as the guiding principle behind all our actions
  • We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit
  • And to do this, we foster a culture of empathy and dynamism
  • People are at the core of our journey over the last few decades

Pay and application dates

A verified salary figure is not established in this article. An online estimate for another Team Member - Manufacturing (Peptide) vacancy is not an offer for reference REF24946S; 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 REF24946S.

Compare your qualifications and experience with the essential conditions for the Pydibimavaram, AP, 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: SAP

For SAP, identify the module or business process and the type of contribution: configuration, development, integration, testing or user support. Give one example that connects the system change to the business need.

Relevant skills

  • SAP
  • GMP
  • quality control
  • quality assurance
  • manufacturing
  • maintenance
  • compliance
  • warehouse operations
  • chemistry

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.

For corrections, see our editorial policy and contact information.