Executive - Quality Control

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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

Responsible for cGMP-compliant QC testing, method validation/transfer activities, laboratory documentation, sample management, GLP/GMP and data integrity compliance, and timely reporting of quality events.

Analysis of Finished products, In-process, Hold time, Raw Materials, stability, and related documentation as per cGMP.

Analytical Method transfer/Validation/Verification activity for new Projects.

Preparation and Standardization of volumetric solutions/ Reagents/ Indicator solution preparation as and when required.

Concurrent documentation of analytical records and storage of raw data, online entries in Instrument/ Equipment’s usage logbooks.

Analysis of Vendor Approval samples.

Implementation of GLP / GMP requirements.

To control and maintain QC Laboratory Records. (Like Laboratory, notebook, Chromatograms, and COA etc.).