Senior QC Executive – Stability & Finished Goods

Piramal Pharma Limited; United Kingdom; On-site; GBP 28,000 - 45,000; Full time

Job summary

Piramal Pharma Solutions in the United Kingdom seeks a Senior Executive-QC to analyze stability and finished product samples in a cGMP environment. You will support the QC section by handling finished products, raw materials, stability testing, and related documentation.

Responsibilities include preparation and standardization of reagents, documentation of analytical results, data entry into logs, and immediate reporting of deviations.

Qualifications

• Analysis of Stability and Finish product samples.
• Receipt/Inward/Storage of QC samples and Disposition of sample after analysis.
• Preparation and Standardization of volumetric solutions/ Reagents/ Indicator solution preparation.

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.
• 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 for new projects.
• 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.
• 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

Attention to detail

Documentation

Tools

GC

UV

Dissolution

Job description

Piramal Pharma Solutions in the United Kingdom seeks a Senior Executive-QC to analyze stability and finished product samples in a cGMP environment. You will support the QC section by handling finished products, raw materials, stability testing, and related documentation.

Responsibilities include preparation and standardization of reagents, documentation of analytical results, data entry into logs, and immediate reporting of deviations.