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.We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries.
- Vacancy details:
- Department: Team Member QC (Nasal)
- Experience: 4 to 8 years
- Qualification: Bachelor’s degree in Chemistry, Analytical Chemistry, Pharmacy and Master in Pharmacy or a related field.
Job Description: Greeting From Dr. Reddy’s Laboratories Ltd. !!!!!!!!
- Important Details :
- Location: Pydibimavaram
- Post of date: 30/07/2024
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to Face
- Interview Rounds of Interview: HR
Job Summary
We are seeking an associate for the Quality team responsible for conducting analysis of Nasal Spray Finished samples and Stability Sample, In use and In process sample. The role involves ensuring accuracy in documentation, adherence to safety procedures, reporting discrepancies, and maintaining lab safety.
Roles & Responsibilities
• You will be responsible for conducting analysis of Nasal Spray(Both solution and suspension) Finished samples, Stability Sample and In process sample and In Use samples as allotted by the group leader.
• You will be responsible for calibration of Nasal related instrument like Spray Tec, Spray view, Osmometer, Microscope as per master schedule.
• 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.
Educational qualification: A Bachelor’s degree in Chemistry, Analytical Chemistry, Pharmacy and Master in Pharmacy or a related field.
Minimum work experience: 4 to 8 years of experience in analysis of Nasal product (Nasal Spray) in the pharmaceutical.
Skills & attributes:
Technical Skills
• Experience with the operation and maintenance of analytical instruments HPLC, UPLC, and “specially Spray tech and Spray View” ensuring proper use and care as per SOPs.
• Expertise in analysis of DSD, DDU and APSD of Nasal Spray.
• 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.
Behavioral 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.
- Vacancy details:
- Department: Team Member – Manufacturing QMS
- Experience: 3 to 5 years
- Qualification: B Pharmacy, M Pharmacy, B Tech, BE
1.1 To ensure and adhere Organization Safety/Quality policies, Procedures and norms effective implementation from time to time.
1.2 Ensure the adherence of SHE standards and policies across the plant with respect to MSI
1.3 Investigation management:
· Ensure to log the incident in SAP/FIORI as per the timelines mentioned in the SOP
· Preparation, review and approval of investigations related to Incident, OOS, OOT, batch failures, Market complaints and recalls.
· Tracking of incident closure and approval of QMS elements within the timelines
· Preparation of trends
1.4 CAPA, change control Quality risk management:
· Log the QMS elements in SAP/FIORI as per the requirement.
· Preparation, review and approval of documents through DOCHUB related to the QMS elements
· Tracking and approval of QMS elements within the timelines
· Preparation of trends for QMS elements
1.5 To review of SOPs, BMR/BPR and all other GMP records as per requirements.
1.6 Audit compliance and Audit management:
· Perform Gap analysis for procedure vs practices
· To participate in GMP/Regulatory Inspections (Internal/External) its compliance.
· Conducting Self inspection and ensure all time audit readiness
1.7 Build organization and people capability by boosting confidence, reduce turnover, increase job security, and stimulate employees to think beyond their role so they can meet future
challenges in a way that adds value to the company and to ensure right first time and Zero Incidents.
1.8 Operational Excellence:
· Preparation and tracking and cost saving policies to reduce of OPEX budget for the plant.
· Improvement plans to improve the quality, safety and efficacy of the product.
· Reducing the complexity and simplifying the activities/ procedures.
1.9 To perform any other task/project assigned by production head from time to time.
Educational qualification: B Pharmacy, M Pharmacy, B Tech, BE
Minimum work experience: 3 to 5 years of experience
