Senior Executive-QC

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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

Senior Executive-QC

Job Description

Analysis of Finished products, Raw Materials, stability, instrument calibrations, WS qualification and related documentation as per cGMP.

• Key Roles/Responsibilities: -
• Analysis of Finished products, Raw Materials, stability, Calibrations , WS qualifications and related documentation as per cGMP.
•  Receipt/Inward/Storage of QC samples.
•  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 log books.
•  Instant reporting in case of any deviation, incident, OOT or OOS to Section Head/ Head QC.
•  Requirement / Procurement of chemical/ reagents/ standards/ columns required for new project.
•  Any additional responsibility assigned by section head.
•  Maintenance of Bin Card of chemical store.
•  Implementation of GLP / GMP requirements.  
•  Allocate works to workmen and trained them.
•  To control and maintain QC Laboratory Records. (Like Laboratory note Book, Chromatograms, and COA etc.).
•  Analysis of Vendor Approval samples.
•  Review of laboratory chemicals.
•  Responsible for analysis in the FTIR, KF Instrument and HPLC Instrument. Does not access to Change the method, report format, cancellation of any run, or system and method configuration.
•  Support to site DICO (Data Integrity Compliance Officer) for monitoring and implementation of actions related to Data Integrity awareness at site.