Dr Reddy’s QA Vacancies – Life Sciences Apply Online Now
Quality Assurance Associate
Location: Hyderabad, Telangana, 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 Summary
We are seeking an individual to verify compliance for activities in the respective counter function regularly. This role involves supporting in establishing the Quality Management Systems, reviewing, and monitoring the performance of Quality Management Systems.
Roles & Responsibilities
Review of procedures relating to Quality Assurance and implementing the global procedures at site with effective training.
Deviation Management System:
- Establishing the deviation management master data in the application and managing changes, facilitating implementation at the site.
- Reviewing daily logged deviations for their category, adequacy of investigations, and taking appropriate actions with line QA.
- Escalating serious deviations for immediate action towards Quality Defect Notification and identifying opportunities for Quality Risk Assessment.
- Conducting dip-stick reviews of closed investigations for appropriate root cause identification and adequate CAPA.
- Performing quarterly trend analysis of deviations for repetitive nature and identifying opportunities for holistic CAPAs.
CAPA Management System:
Reviewing the adequacy of Corrective Actions and Preventive Actions and periodically discussing them with line functions for adequacy.
Change Management System:
- Reviewing change controls for category, adequacy of supportive documents, and post-change effectiveness requirements.
- Coordinating change control review meetings for all significant changes across QA Leads and QPs.
- Tracking change controls for regulatory notification and their implementation.
Daily Routine Logs:
Maintaining daily routine logs and developing the team to analyze the data meaningfully.
Training Facilitation:
Facilitating training across quality management systems, including digital systems and processes.
Quality Risk Management System:
- Reviewing Quality Risk Assessments for mitigation plans and creating a risk register for the site.
- Communicating high risks to the senior leadership team.
Qualifications
- Educational Qualification: A B.Pharm. or Post-Graduation (Life Sciences).
- Minimum Work Experience: 6-8 years of industrial experience with specific operational experience in Manufacturing, Quality Control, Quality Assurance, or Engineering.
Skills & Attributes
Technical Skills
- Solid understanding of Quality Systems and ability to comprehend and navigate counter functions within the organization.
- Ability to develop simplified and robust quality systems.
- Troubleshooting issues with simple solutions.
- Knowledge of the Bio Pharma and Pharma markets, including product knowledge, market trends, competitors, and customer needs.
- Familiarity with global cGMP regulatory requirements (FDA, EU, Indian authorities).
- Awareness of broader market dynamics, industry trends, and factors influencing the pharmaceutical market.
- Understanding and implementing organizational policies to ensure compliance.
Behavioral Skills
- Commitment to continuous learning.
- Strong communication and influencing skills.
- Analytical and logical thinking abilities.
- Self-motivated and takes initiative.
- Adaptability to the work environment and being a team player.
- Proactive and innovative approach to going beyond boundaries.
Keywords: Quality Assurance Associate, Dr. Reddy’s Laboratories, Pharmaceutical, Quality Systems, Compliance, Regulatory Requirements. Dr Reddy’s QA Vacancies – Life Sciences Apply Online Now. Please ensure you are subscribed to the Biotecnika Times Newsletter and our YouTube channel to be notified of the latest industry news. Follow us on social media like Twitter, Telegram, Facebo
