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Division
Piramal Pharma SolutionsPiramal 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 Title
Executive-QCJob Description
Responsible for sampling, analysis, and testing of in-process, intermediate, and stability samples using UV and HPLC techniques. Ensure compliance with cGMP, SOPs, and documentation requirements while supporting investigations related to deviations and OOS results.
- Perform analysis of in-process, intermediate, and stability samples as per SOPs.
- Conduct UV and HPLC analysis in rotational shifts.
- Handle stability sample charging, withdrawal, and analysis.
- Prepare stability protocols and reports.
- Perform hold-time study sample analysis.
- Maintain analytical records and documentation as per cGMP requirements.
- Support investigations of deviations and Out of Specification (OOS) results.
- Handle reporting authority responsibilities in their absence.
- Perform additional responsibilities as assigned by seniors.
cGMP Regulations, High-Performance Liquid Chromatography (HPLC), Out of Specifications, Quality Control (QC), Sample Analysis, Standard Operating Procedure (SOP)