Hiring QC Investigation Team Member at Dr. Reddys Laboratories

Dr. Reddys Laboratories is an Indian multinational pharmaceutical company located in Hyderabad, Telangana, India. The company was founded by Kallam Anji Reddy, who previously worked in the mentor institute Indian Drugs and Pharmaceuticals Limited.

Post : Team Member - QC Investigation

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
• You will be responsible for investigations of quality notifications like OOT, OOS, Incidents.
• Shall able to drive the investigation step to step till closure of incidents or quality notifications.
• Shall be able to track CAPA's Assigned to the individual team member.
• Shall be responsible for implementation of CAPA and CAPA effectiveness check.
• You will be responsible for testing and Release of RM,PM materials as per the production requirement.
• You will be responsible for SAP activities, ROA (Record of Analysis) preparation, and reviewing analytical records and raw data against Specification and STP (Standard Testing Protocol).
• You will ensure accuracy of the documentation before submitting it for the Group Leader’s review or uploading online.
• 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.

Candidate Profile
• A Bachelor’s degree in Chemistry, Analytical Chemistry, or a related field
• MSC, M.Pharmacy, B.Pharmacy
• 6 to 9 years of experience in a laboratory setting, preferably in the pharmaceutical or related industry
• Proficient Communication Skills required for designing the investigation reports.
• 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 : 6 to 9 years
Qualification : MSC,M Pharmacy, B Pharmacy
Location : Visakhapatnam
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Quality Control - GMO
End Date : 20th July 2024