Senior Executive-QC

Piramal Pharma Ltd; India; On-site; INR 400,000 - 600,000; Full time

Job summary

Piramal Pharma Solutions is a leading CDMO, delivering end-to-end development and manufacturing services across the drug life cycle. The Senior Executive-QC will contribute to cGMP-compliant analysis of finished products, raw materials, and stability data, while ensuring proper documentation and data integrity at site.

The role involves handling QC samples, preparing standards, maintaining records, and reporting deviations.

Qualifications

• Experience in cGMP compliant laboratory practices and documentation.
• Receipt, storage, and disposition of QC samples.
• Ability to report deviations and maintain laboratory records.

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.

Skills

Analytical thinking

Attention to detail

Team coordination

Tools

GC

Dissolution

UV

Job description

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 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.