New Pharma Job Alert! Dr Reddy’s is hiring for an Analytical Quality Assurance Associate role | Apply Now
Looking for a promising Quality Assurance Job in the pharmaceutical industry? Dr Reddy’s Careers brings an excellent opportunity for professionals through the Analytical Quality Assurance Associate role in Hyderabad. This Pharma Job offers candidates the chance to work in biologics, analytical research, and quality systems while contributing to innovative healthcare solutions at a globally recognised pharmaceutical organisation.
- Job Title: Analytical Quality Assurance Associate
- Location: Hyderabad, Telangana, India
About the Company
Dr Reddy’s careers is a globally recognised multinational pharmaceutical company headquartered in Hyderabad, India. Founded in 1984, the company has grown from a small startup with limited employees into one of India’s leading pharmaceutical organisations focused on providing affordable and innovative medicines worldwide.
The company operates across research & development, manufacturing, and commercialisation, serving patients in more than 75+ countries through a strong global presence. Its business spans generic medicines, branded generics, biosimilars, active pharmaceutical ingredients (APIs), and over-the-counter healthcare products, addressing major therapeutic areas such as oncology, cardiovascular diseases, diabetes, gastroenterology, pain management, and dermatology.
Key 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 minimised 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 organisation’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: A Graduation or post-graduation in Science, including 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.
