Apply Online for Quality Control Team Member at Dr. Reddy’s Laboratories

Dr.Reddy's Laboratories offers a competitive total rewards package including base salary determined on the basis of role, experience, skill set and location. Additionally, employees are eligible for an annual discretionary bonus, and benefits including comprehensive health care coverage, retirement savings plan and leave benefits. Additional details about total compensation and benefits will be provided during the hiring process.

Post : Team Member - Quality Control (RM/PM)

Job Description
Job Summary :
We are seeking a competent and detail-oriented QC Analyst – RM & PM to perform testing of Raw Materials and Packing Materials in compliance with regulatory requirements and internal quality standards. The candidate should be well-versed in analytical techniques and instrument handling.

Key Responsibilities :
You will also be responsible for Perform analysis of Raw Materials (RM) and Packing Materials (PM) as per approved specifications and test methods.
• You will also be responsible to Operate and troubleshoot analytical instruments including:
o HPLC (High Performance Liquid Chromatography)
o GC (Gas Chromatography)
o Auto Titrator
o Karl Fischer (KF)
o UV-Visible Spectrophotometer
o FTIR Spectrophotometer
• You will also be responsible to Ensure compliance with GMP, GLP, and data integrity (ALCOA+) principles.
• You will also be responsible to Review and record analytical data in compliance with approved procedures.
• You will also be responsible to Perform calibration/verification of laboratory instruments as per schedule.
• You will also be responsible to Support investigations related to OOS, OOT, and deviations.
• You will also be responsible to Ensure proper documentation, logbook entries, and traceability of all activities.
• You will also be responsible to Maintain laboratory safety standards and good housekeeping practices.
• You will also be responsible for the proper use and care of instruments or equipment as instructed in relevant SOPs (Standard Operating Procedure), including cleaning before and after analysis.
• You will adhere to safety precautions and procedures during analysis.
• Your responsibilities include placing SOP/STP/reference standards at their designated locations after analysis, and reporting discrepancies or incidents promptly to the Group Leader.
• Lab safety, following JSA (Job Safety Analysis), and using proper PPE (Personal Protection Equipment) at the workplace are emphasized.
• You will oversee the handling and upkeep of the chemical and solvent store, preparation of Spec-check, catalog, and result entries, as well as maintaining volumetric solutions and reagents.
• Your role also includes preparation of out lab testing samples (as required), timely destruction of samples as per SOP, printing COA (Certificate of Analysis), completing assigned training, and any additional responsibilities assigned by the Group Leader.

Qualifications
Educational qualification : A Master’s degree in Chemistry, Analytical Chemistry, or a related field
Minimum work experience : 3 to 6 years of experience in a laboratory setting, preferably in the pharmaceutical or related industry.

Skills & attributes :
Technical Skills
• Proficient in various analytical techniques, including sampling and analysis of packaging and raw material samples.
• Experience with the operation and maintenance of analytical instruments, ensuring proper use and care as per SOPs.
• Competent in SAP activities related to sample tracking, documentation, and data entry.
• Knowledgeable about cGMP, SOPs, and STPs, ensuring accurate documentation and adherence to specifications.
• Adheres to safety precautions and procedures during analysis, emphasizing the importance of lab safety, JSA (Job Safety Analysis), and proper use of PPE (Personal Protective Equipment).
• Expertise in handling and upkeep of the chemical and solvent store, including the preparation and maintenance of volumetric solutions and reagents.

Behavioural Skills
• Keen attention to detail in analysis and documentation, ensuring accuracy in all tasks.
• Effective communication and collaboration skills for communicating with the Group Leader, reporting discrepancies, incidents, and providing timely updates.
• Takes initiative in ensuring the proper use and care of instruments, timely destruction of samples, and other assigned responsibilities.
• Demonstrates problem-solving skills in addressing discrepancies, incidents, and ensuring smooth laboratory operations.
• Upholds ethical standards, compliance with SOPs, and follows regulatory requirements in all activities.

Additional Information
Experience : 3 to 6 years
Qualification : Master’s degree in Chemistry, Analytical Chemistry
Location : Baddi, India
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Quality Control (RM/PM)
End Date : 30th August 2026