Pharma Jobs at Dr Reddy’s: AQA Associate Role | Dr Reddy’s Careers
Explore the latest Pharma Jobs at Dr Reddy’s Laboratories with this AQA Associate opportunity in Hyderabad. This opening under Dr Reddy’s Careers is ideal for science graduates and postgraduates looking to build strong careers through full-time, on-site roles in quality and biologics research within the pharmaceutical industry.
- Job Title: AQA Associate
- Location: Hyderabad, Telangana, India
About the Company
Dr. Reddy’s Laboratories Ltd. is a leading Indian multinational pharmaceutical company headquartered in Hyderabad, Telangana, founded in 1984 by Dr. K. Anji Reddy. The company develops, manufactures, and markets a wide range of generic medicines, branded formulations, active pharmaceutical ingredients (APIs), biosimilars, and OTC products across key therapy areas, including oncology, cardiovascular, gastroenterology, diabetology, and dermatology. With a strong global footprint across regulated and emerging markets, Dr. Reddy’s serves millions of patients worldwide and is driven by its purpose, “Good Health Can’t Wait,” focusing on affordable, accessible, and innovative healthcare solutions.
Job Description
Roles & Responsibilities
- Responsible for preparing necessary documents before experiments, including calculations for working stocks and reagent preparations, data templates, etc. Ensuring the availability of prerequisites (reagents and information) before executing experiments for the smooth execution of the given experiment.
- Executing experiments with minimized technical errors, according to defined Standard Operating Procedures (SOP) and development plans in compliance with safety and quality norms. Ensuring the generation of high-quality data and meeting project requirements as defined by the supervisor.
- Contemporaneous, accurate, legible, attributable, and original data documentation of day-to-day execution. Adhering to the organization’s quality management system and ensuring data reproducibility.
- Identifying and notifying the supervisor of any out-of-trend data and being involved in writing SOP/SDP (Standard Documentation Procedure)/any work instruction documents.
Qualifications
Educational qualification and work experience
- Educational qualification: A Graduation or post-graduation in Pharma and Technology.
- Minimum work experience: 3 to 8 years of Academic or Industrial experience.
Skills & Attributes
Technical Skills
- Basic understanding of relevant techniques, including cell-based and ligand binding assays. Familiarity with fundamental biotechnology industry practices.
- Understanding of protein-protein interactions, encompassing principles of ELISA (Enzyme-Linked Immunosorbent Assay), electrophoresis, and western blotting techniques.
- Knowledge of animal cell culture techniques, including the handling, maintenance, and propagation of cell lines.
Behavioural skills
- Learning orientation, seeking opportunities for personal and professional development.
- Stakeholder orientation focuses on understanding and meeting the needs of various stakeholders involved.
- Ability to build relationships, fostering positive connections with colleagues, clients, and other stakeholders.
