Intas Pharma R&D Jobs – Chemistry & Pharma Apply Online
Research and Development Associate
Location: Ahmedabad, Gujarat, India
About the Job
Education Experience: Master of Pharmacy or Master of Chemistry
Required Experience: 03-08 years of Analytical research and development experience in development, validation, and transfer of analytical methods
Key Responsibilities and Areas of Expertise:
Method Development & Validation and Analysis:
- Conduct analysis using various analytical instruments and development of methods and validation.
- Perform analysis of various samples adhering to the approved methods and pharmacopoeia standards.
- Respond to queries related to analytical methods/procedures.
- Prepare detailed analytical method development reports and protocols.
Instrument Operation & Calibration:
- Operate and calibrate instruments such as HPLC, GC / Other Analytical instruments as per established and approved procedures.
- Calibrate analytical instruments as per established schedules.
- Handle troubleshooting and resolve issues in analytical processes, instruments, and equipment.
- Develop analytical techniques.
Documentation & Compliance:
- Adhere to good documentation practices and ensure compliance with regulatory standards.
- Ensure accuracy of results, interpretation of chromatographic data, and preparation of precise reports/log-books.
Project Communication:
- Provide regular/periodical updates on work status and communicate any project-related issues promptly to team lead/hierarchy.
- Lead analytical problem-solving initiatives and comply with GLP requirements.
Knowledge of Regulatory Norms, QMS, and Working Standards:
- Stay updated with relevant regulatory standards (e.g., USP, ICH / Other Regulatory) and incorporate new techniques into practices.
- Implement continuous process improvements.
Analysis and Interpretation of Results:
- Support routine analysis and interpretation of analytical results, ensuring compliance with Good Laboratory Practice (GLP) standards and laboratory safety.
- Analyze results to identify gaps and opportunities for further process improvements.
Knowledge of QMS Requirements: Manage storage and retrieval of data/results.
Areas of Expertise:
- Analytical method development, validation, and transfer
- Instrument troubleshooting, calibration, and maintenance
- Ensuring cGMP compliance and documentation as per regulatory standards
- Maintaining reference standards and performing literature reviews
- Coordination across departments and resolving technical issues
- QMS, GLP, and laboratory safety
- Chromatographic techniques
