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Division
Piramal Pharma Solutions
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 Title
Executive-QC
Job Description
Experienced Quality Control Analyst with expertise in sampling and analysis of in-process, stability, and hold-time study samples using UV and HPLC instruments as per SOPs and cGMP requirements. Skilled in stability program management, including sample charging/withdrawal, protocol and report preparation, and maintaining accurate documentation. Proficient in supporting deviation and OOS investigations, working in rotating shifts, and handling reporting authority responsibilities in the absence of supervisors while effectively supporting cross-functional laboratory operations.
- Analysis of in-process samples.
- Sampling and analysis of intermediate samples as per SOPs and in-house procedures.
- Sampling and analysis of stability samples.
- Charging and withdrawal of stability samples.
- Preparation of stability protocols and reports.
- Analysis of hold time study samples.
- Maintaining documentation as per cGMP requirements.
- Handling responsibilities of reporting authority in their absence.
- Performing any other work allocated by seniors.
- Perform UV and HPLC analysis in rotating shifts as per SOPs.
- Support the investigation of deviations and Out of Specification (OOS) results.
