Senior Executive-QC

Piramal Pharma Ltd; India; On-site; INR 600,000 - 900,000; Full time

Job summary

Piramal Pharma Solutions is hiring a Senior Executive-QC in India to perform stability and finished product analysis in a cGMP environment. The role involves handling QC samples, preparing reagents, maintaining records, and ensuring data integrity.

The incumbent will support the section head, manage laboratory documentation, and contribute to GLP/GMP implementation across the site. This position focuses on accuracy, compliance, and timely reporting of deviations.

Responsibilities

• Analysis of Finished products, Raw Materials, stability and related documentation as per cGMP.
• Receipt/Inward/Storage of QC samples and Disposition of sample after analysis.
• 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/ Equipments 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 only run the method in the GC, Dissolution & UV 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.

Job description

Division

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 Stability and Finish product samples.

• Analysis of Finished products, Raw Materials, stability and related documentation as per cGMP.
• 2. Receipt/Inward/Storage of QC samples and Disposition of sample after analysis.
• 3. Preparation and Standardization of volumetric solutions/ Reagents/ Indicator solution preparation as and when required.
• 4. Concurrent documentation of analytical records and storage of raw data, Online entries in Instrument/ Equipments usage log books.
• 5. Instant reporting in case of any deviation, incident, OOT or OOS to Section Head/ Head QC.
• 6. Requirement / Procurement of chemical/ reagents/ standards/ columns required for new project.
• 7. Any additional responsibility assigned by section head.
• 8. Maintenance of Bin Card of chemical store.
• 9. Implementation of GLP / GMP requirements.
• 10 Allocate works to workmen and trained them.
• 11. To control and maintain QC Laboratory Records. (Like Laboratory note Book, Chromatograms, and COA etc.).
• 12. Analysis of Vendor Approval samples.
• 13. Review of laboratory chemicals.
• 14. Responsible for only run the method in the GC, Dissolution & UV does not access to Change the method, report format, cancellation of any run, or system and method configuration.
• 15. Support to site DICO (Data Integrity Compliance Officer) for monitoring and implementation of actions related to Data Integrity awareness at site.