Dr. Reddy’s Careers: Quality Assurance Jobs | Apply Now
Are you looking for Quality Assurance Jobs or M.Sc Chemistry Jobs in the pharmaceutical industry? Dr. Reddy’s Laboratories, Ranastalam, invites applications for the position of Team Member – Quality Assurance (Validation). This role is ideal for professionals seeking hands-on experience in process validation, GMP compliance, and pharmaceutical manufacturing operations. Join Dr. Reddy’s Careers and contribute to delivering high-quality medicines to millions of patients worldwide, while advancing your professional growth in a global, innovative environment.
About Dr. Reddy’s Laboratories Ltd.
Dr. Reddy’s Careers provides professionals with opportunities in Quality Assurance Jobs, M.Sc Chemistry Jobs, and Validation roles across global manufacturing operations. Employees gain hands-on experience in GMP compliance, regulatory adherence, and pharmaceutical manufacturing processes, contributing to life-saving medicines worldwide. With a culture focused on growth, innovation, and sustainability, Dr. Reddy’s empowers talent to advance their careers while making a meaningful impact on global healthcare.
Job Description
Job Summary
We are seeking an individual for the Quality Assurance team, responsible for overseeing various quality assurance activities to ensure compliance with regulatory requirements and maintain product quality. Your responsibilities will include managing change notifications, conducting investigations, handling market complaints, coordinating audits, and supporting regulatory
filings.Roles & Responsibilities
- Review of Technology transfer documents, Review of process and cleaning trial and validation documents, nitrosamine impurity assessments, CPV reports, batch production records, and cleaning records, etc.
- Reviewing and approving Quality Risk Management processes to identify, assess, and mitigate risks to product quality and patient safety.
- Performing SAP activities and updating Bills of Materials (BOM) and recipes accurately to reflect product specifications and changes.
- Monitoring plant activities related to trials and Validations.
- Supporting marketing queries and DMF filings.
- Ensuring compliance with good manufacturing practice (GxP) and other regulatory requirements through self-training and adherence to established procedures.
Qualifications
- Educational qualification: M.Sc in Chemistry.
- Minimum work experience: 3 to 12 years of experience in pharmaceutical manufacturing or a similar role
Skills & Attributes
Technical Skills
- Knowledge of process and cleaning validation activities, sampling and relevant standards.
- Proficiency in performing line clearance, material verification, start-up checks, and in-process checks following batch manufacturing and packing records.
- Experience in timely sampling and testing of in-process, reserve, and finished samples, as well as stability samples and environmental monitoring.
- Skilled in reviewing batch manufacturing and batch packing records, ensuring accuracy and certification after execution.
