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Job Responsibilities** * Perform analytical testing of raw materials, in-process samples, and finished products using various analytical techniques (e.g., HPLC, GC, UV-Vis, FTIR, dissolution, titrations). * Review and interpret analytical data, ensuring accuracy and completeness of results. * Document all analytical procedures, results, and observations in accordance with cGMP and company guidelines. * Troubleshoot and resolve analytical instrument issues investigations. * Develop, validate, and transfer analytical methods as required. * Participate in internal and external audits, providing necessary documentation and support. * Ensure compliance with all relevant regulatory requirements . * Maintain laboratory equipment and ensure calibration schedules are followed. * Contribute to continuous improvement initiatives within the Quality Control department.
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Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle.
We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.
This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms.
We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation.
Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide.
For more details, please visit : www.piramalpharmasolutions.com
Job Responsibilities** * Perform analytical testing of raw materials, in-process samples, and finished products using various analytical techniques (e.g., HPLC, GC, UV-Vis, FTIR, dissolution, titrations). * Review and interpret analytical data, ensuring accuracy and completeness of results. * Document all analytical procedures, results, and observations in accordance with cGMP and company guidelines. * Troubleshoot and resolve analytical instrument issues investigations. * Develop, validate, and transfer analytical methods as required. * Participate in internal and external audits, providing necessary documentation and support. * Ensure compliance with all relevant regulatory requirements . * Maintain laboratory equipment and ensure calibration schedules are followed. * Contribute to continuous improvement initiatives within the Quality Control department.
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Global pharmaceutical company specializing in CDMO, complex hospital generics, and consumer healthcare.
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