Team Member QC Job at Dr Reddy’s Labs – Apply Online
Team Member – Quality Control
Baddi, Himachal Pradesh, India
About the job
Company Description
Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait.
Job Description
Job Summary
We are seeking an associate for the Quality team responsible for conducting sampling and analysis of packaging and raw material samples. The role involves ensuring accuracy in documentation, adherence to safety procedures, reporting discrepancies, and maintaining lab safety.
Roles & Responsibilities
- Conduct sampling and analysis of IP/FP, Stability, packaging, and raw material samples as allotted by the group leader.
- Responsible for SAP activities, ROA (Record of Analysis) preparation, and reviewing analytical records and raw data against Specification and STP (Standard Testing Protocol).
- Ensure accuracy of documentation before submitting it for the Group Leader’s review or uploading it online.
- Proper use and care of instruments or equipment as instructed in relevant SOPs (Standard Operating Procedures), including cleaning before and after analysis.
- Adhere to safety precautions and procedures during analysis.
- Place SOP/STP/reference standards at their designated locations after analysis and promptly report discrepancies or incidents to the Group Leader.
- Ensure lab safety, follow JSA (Job Safety Analysis), and use proper PPE (Personal Protection Equipment) at the workplace.
- Oversee handling and upkeep of the chemical and solvent store, prepare Spec-check, catalog, result entries, and maintain volumetric solutions and reagents.
- Prepare out-lab testing samples (as required), ensure timely destruction of samples as per SOP, and print COA (Certificate of Analysis).
- Complete assigned training and any additional responsibilities assigned by the Group Leader.
Qualifications
- Educational qualification:
- A Bachelor’s degree in Chemistry, Analytical Chemistry, or a related field
- Minimum work experience:
- 2 to 5 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 lab safety, JSA (Job Safety Analysis), and proper use of PPE (Personal Protection 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.
