Associate
1 week ago
Company Description
Aurobindo Pharma Limited is a globally integrated pharmaceutical company headquartered in Hyderabad, India, operating in over 150 countries. Renowned as the largest generic pharmaceutical company in the United States, Aurobindo Pharma specializes in generic pharmaceuticals, branded specialty drugs, and active pharmaceutical ingredients (APIs). With over 30 advanced manufacturing and packaging facilities approved by global regulatory authorities like USFDA, UK MHRA, and WHO, the company prioritizes quality and compliance. Its diverse product portfolio encompasses eight key therapeutic areas, including CNS, ARV, CVS, and Oncology. Innovation is driven by a strong R&D infrastructure focused on affordability and accessibility.
Role Description
This is a full-time on-site Associate role, located in Hyderabad. The Associate will be responsible for supporting the development, manufacture, and quality assurance of pharmaceutical products. The candidate will assist in routine analysis, process monitoring, documentation, and compliance with regulatory standards. Collaboration with cross-functional teams and adherence to industry best practices are key components of this role. Additional tasks may include contributing to process optimization and supporting research and development activities as needed.
Qualifications
- Proficiency in Pharmaceutical Manufacturing, Quality Control, and Quality Assurance processes
- Research and Development skills with a focus on data analysis and innovation
- Strong organizational, documentation, and process monitoring skills
- Knowledge of regulatory guidelines and compliance standards, including USFDA and WHO requirements
- Attention to detail, problem-solving skills, and ability to work collaboratively
- Bachelor's degree in Pharmacy, Chemistry, Biotechnology, or a related field
- Relevant pharmaceutical industry experience is preferred
- Familiarity with Good Manufacturing Practices (GMP) and other pharmaceutical industry best practices
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