Dr. Reddy’s Laboratories Ltd. is an Indian multinational pharmaceutical company based in Hyderabad, with U.S. headquarters in East Brunswick, New Jersey. The company was founded by Kallam Anji Reddy, who previously worked in the mentor institute Indian Drugs and Pharmaceuticals Limited.
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.
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Job Description:
We are seeking a detail-oriented and analytical Team Member for our Quality Control (QC) department to join our Quality Management System (QMS) team in Visakhapatnam, India. In this role, you will play a crucial part in ensuring our products and processes meet the highest quality standards.
- Implement and maintain quality control procedures within the QMS framework
- Conduct thorough inspections and tests on products and materials at various stages of production
- Analyze quality data and prepare comprehensive reports for management review
- Identify and document quality issues, proposing corrective actions when necessary
- Collaborate with cross-functional teams to improve product quality and manufacturing processes
- Ensure compliance with industry standards, regulations, and company policies
- Participate in quality improvement initiatives and projects
- Maintain accurate and up-to-date quality control documentation
- Assist in internal and external quality audits as required
Qualifications:
- Bachelor’s degree in Engineering, Quality Management, or a related field
- Proven experience in quality control or quality assurance, preferably in a manufacturing environment
- Strong knowledge of quality control methodologies and QMS principles
- Proficiency in using QMS software and quality control tools
- Excellent data analysis and reporting skills
- Meticulous attention to detail and strong problem-solving abilities
- Effective communication skills, both verbal and written
- Familiarity with industry-specific quality standards and regulations
- Experience with statistical process control and continuous improvement techniques
- Quality management certifications (e.g., Six Sigma, ISO 9001) preferred
- Ability to work efficiently in a fast-paced, team-oriented environment
- Willingness to adapt to changing priorities and deadlines
Role :
- Qualifications: B.Pharm / M.Pharm / M.Sc in Chemistry or related disciplines
- Experience: Minimum 5 years in Quality Control (QMS within sterile/injectables manufacturing
Skills:
- Strong understanding of QMS documentation & regulatory comp-
- Experience in handling deviations, change controls, CAPA & audit )readiness
- Familiarity with sterile manufacturing processes & GMP guidelines
- Proficiency in LIMS, TrackWise & other QMS tools.
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