Quality Control Associate - Molecular Biology

Dr Reddy's Laboratories Limited; Hyderabad; Sur place; INR 1 200 000 - 2 400 000; Plein temps

Résumé du poste

Dr Reddy's Laboratories Ltd. in Hyderabad, India, is seeking a detail-oriented Quality Control Associate (Molecular Biology) to join the Biologics unit.

The role focuses on planning and executing a range of QC assays for batch release and stability, with strict adherence to cGMP practices and comprehensive documentation. The candidate will collaborate with cross-functional teams to drive quality improvements, maintain lab safety, and address deviations through proper investigations, contributing

Qualifications

• Masters in Biotechnology, Microbiology, Biochemistry or related field.
• 6-9 years of experience in quality control or related field.
• Strong knowledge of QC methodologies and statistical analysis.
• ASQ certification or other QC certifications preferred.

Responsabilités

• Plan and execute SDS-PAGE, Western Blot, Dot Blot, IEF and related assays for batch release and stability.
• Plan and execute ELISA techniques such as HCP and Pro A for batch release and stability.
• Report lab deviations and OOS/OOT and address investigations.
• Maintain accurate QC documentation and records.
• Calibrate and maintain QC equipment to ensure testing accuracy.
• Collaborate with cross-functional teams to improve QC processes.
• Ensure compliance with cGMP, SHE, industry standards and company policies.

Description du poste

Quality Control Associate - Molecular Biology

• Full-time
• Job Family: Quality
• Sub Job Family: Quality Control
• Preferred type of working: On-Premise
• Business unit: Biologics

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.

For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. Asthepharmaceutical industry evolves and undergoes disruption, we see an opportunity –tostrengthen our core further (the next steps) and to build the future (the new bets).

‘TheNextand the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency

Dr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization.

We are seeking a detail-oriented and analytical Quality Control Associate to join our team in Hyderabad, India. In this role, you will be responsible for ensuring that our products meet the highest quality standards through rigorous testing, inspection, and data analysis.

• To Plan and execute SDS-PAGE, Western Blot, Dot Blot, IEF, assays for batch release and stability with in defined TAT.
• To Plan and execute HCD, Mycoplasma(RT-PCR) assays for batch release and stability with in defined TAT.
• To Plan and execute ELISA techniques like HCP and Pro A ELISA assays for batch release and stability with in defined TAT.
• To Plan and execute CE-SDS and CZE assays for batch release and stability with in defined TAT.
• To plan and execute Physicochemical, Biochemical assays for batch release and stability with in defined TAT
• To comply and maintain the laboratory with cGMP practices.
• To adhere and follow the safety practices and procedure as per SHE.
• To report Laboratory failures, Deviations, OOS, OOT upon observation and address the same through proper investigation.
• Maintain accurate and up-to-date quality control documentation and records
• Collaborate with cross-functional teams to implement and improve quality control processes
• Monitor and ensure compliance with industry standards, regulations, and company policies
• Participate in continuous improvement initiatives to enhance product quality and efficiency
• Calibrate and maintain quality control equipment to ensure accuracy in testing
• Assist in developing and updating quality control procedures and protocols
• Train and guide team members on quality control best practices and procedures

• Masters degree in Biotechnology/Microbiology/Biochemistry, or a related field
• 6-9years of experience in quality control or a related field
• Strong knowledge of quality control methodologies and statistical analysis
• Proficiency in quality control software and data management tools
• Familiarity with industry standards and regulations relevant to manufacturing
• Excellent attention to detail and analytical skills
• Strong problem-solving abilities and critical thinking skills
• Effective communication skills, both verbal and written
• Experience with manufacturing processes and quality management systems
• ASQ certification or other relevant quality control certifications preferred
• Ability to work efficiently in a fast-paced environment
• Strong organizational skills and ability to manage multiple priorities