Executive-QC

Piramal Pharma Ltd; Navi Mumbai; On-site; INR 350,000 - 600,000; Full time

Job summary

Piramal Pharma Solutions in Navi Mumbai is seeking an Executive-QC to perform sampling and analysis across in-process, intermediate, and stability samples. The role requires UV and HPLC analyses per established SOPs and strict cGMP documentation practices.

You will support deviation and OOS investigations, rotate shifts, and ensure quality records are maintained for regulatory compliance. This position offers on-site work at our Navi Mumbai facility.

Qualifications

• Sampling and analysis of in-process, intermediate, stability, and hold-time study samples.
• Proficient in UV and HPLC analyses as per SOPs.
• Maintain cGMP-compliant documentation and records.

Responsibilities

• Perform analysis of in-process, intermediate, stability, and hold-time study samples.
• Conduct UV and HPLC analysis as per SOPs and in-house procedures.
• Handle charging and withdrawal of stability samples.
• Prepare stability study protocols and reports.
• Maintain all analytical records and documentation as per cGMP requirements.
• Support investigations related to deviations and OOS results.
• Perform reporting authority responsibilities in their absence.
• Work in rotating shifts as required.
• Perform other duties assigned by seniors.

Skills

UV analysis

HPLC analysis

cGMP documentation

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

Executive-QC

Job Description

Responsible for sampling and analysis of in-process, intermediate, stability, and hold-time study samples using UV and HPLC as per SOPs. Prepare stability protocols and reports, maintain cGMP-compliant documentation, support deviation and OOS investigations, and perform other assigned QC activities, including rotating shifts.

• Perform analysis of in-process, intermediate, stability, and hold-time study samples.
• Conduct UV and HPLC analysis as per SOPs and in-house procedures.
• Handle charging and withdrawal of stability samples.
• Prepare stability study protocols and reports.
• Maintain all analytical records and documentation as per cGMP requirements.
• Support investigations related to deviations and Out of Specification (OOS) results.
• Perform reporting authority responsibilities in their absence.
• Work in rotating shifts as required.
• Perform other duties assigned by seniors.
  cGMP Regulations, High-Performance Liquid Chromatography (HPLC), OOS Investigations, Out of Specifications, Stability Protocol