Life Science Jobs at Dr. Reddy’s Laboratories
Searching for high-growth Life Science Jobs in the pharmaceutical industry? Here is a golden opportunity from Dr. Reddy’s Laboratories for talented candidates passionate about analytical testing, GMP compliance, and quality assurance. This latest opening under Dr. Reddy’s Jobs is perfect for professionals looking for stable quality control jobs and an excellent opportunity for life science graduates to build a rewarding career in one of India’s leading pharma companies.
About the Company
Dr. Reddy’s Laboratories is one of the world’s leading pharmaceutical companies with operations in over 66 countries. Founded in 1984, the company focuses on affordable and innovative healthcare solutions. Dr. Reddy’s Jobs are highly preferred among professionals seeking long-term pharmaceutical careers, advanced learning opportunities, and rewarding Life Science Jobs in India and globally.
Job Details:
- Job Title: Quality Control Associate – In-Process
- Company: Dr. Reddy’s Laboratories
- Location: Hyderabad
- Employment Type: Full-Time
Overview
The Quality Control Associate – In-Process will be responsible for planning and executing biochemical and physicochemical assays for batch release and stability studies within defined turnaround timelines. The role also involves analytical instrument maintenance, compliance management, audit readiness, and collaboration with cross-functional teams to ensure quality and operational excellence in pharmaceutical manufacturing.
Key Responsibilities
- Perform biochemical and physicochemical assays for batch release and stability testing within defined turnaround time (TAT).
- Conduct physicochemical analyses including:
- Protein estimation
- Moisture content analysis
- pH testing
- Physical appearance assessment
- Sub-visible particle measurement
- Reconstitution testing of lyophilized vials
- Extractable volume testing
- General product description evaluation
- Carry out scheduled calibration and maintenance of analytical instruments.
- Perform breakdown analysis and support preventive maintenance activities.
- Collaborate with cross-functional teams to resolve quality discrepancies and implement corrective and preventive actions (CAPA).
- Ensure compliance with GMP standards, safety procedures, and Standard Operating Procedures (SOPs).
- Maintain audit readiness and support Quality Management System (QMS) activities including documentation, training, and CAPA closure.
Educational Qualifications
Graduation or Post-Graduation in:
- Biochemistry
- Biotechnology
- Microbiology
Experience Required
2 to 6 years of relevant industry experience in pharmaceutical quality control or related functions.
Technical Skills
- Audit Management
- Current Good Manufacturing Practices (cGMPs)
- Lean Methodologies
- Risk Management
- Total Productive Maintenance (TPM)
Behavioral Competencies
- Strong accountability and ownership mindset.
- Strategic and data-driven problem-solving approach.
- Focus on people development, coaching, and team collaboration.
Benefits & Work Culture
Dr. Reddy’s Laboratories offers a collaborative and inclusive work environment focused on innovation, professional development, and employee well-being. Benefits include:
- Personalized learning and career development programs
- Joining and relocation support
- Maternity and paternity benefits
- Medical insurance coverage for employees and families
- Life insurance coverage
- Exposure to global pharmaceutical operations and cross-functional collaboration
The organization promotes a purpose-driven culture centered around improving access to affordable and innovative healthcare solutions worldwide.
