Job Description

1. IPQA / Shop Floor Activities Perform In-Process Quality Assurance (IPQA) activities in production and packing areas. Verify line clearance before commencement of manufacturing and packing operations. Ensure compliance with approved BMR/BPR, SOPs, specifications, and process parameters. Monitor critical manufacturing and packing activities and perform required in-process checks. Verify equipment and area status before and during operations. Ensure proper identification and status labeling of materials, products, and equipment. Monitor compliance with GMP, hygiene, gowning, and housekeeping requirements. Report and document any deviation, incident, or non-compliance observed on the shop floor. 2. Batch Documentation Review manufacturing and packing records for completeness and compliance. Verify entries for accuracy, traceability, and data integrity. Ensure corrections in GMP documents are made as per approved procedures. Review equipment and area logbooks as applicable. Support batch record review and compilation for QA disposition. 3. Deviation, CAPA & Change Control Initiate and support investigation of deviations, incidents, and non-conformances. Assist in root-cause analysis and evaluation of impact. Support preparation, implementation, and monitoring of CAPA. Review and monitor change-control activities related to manufacturing and quality systems. Track assigned quality-system actions for timely closure. 4. Sampling & In-Process Checks Perform or coordinate in-process sampling and checks as per approved procedures. Coordinate with QC for testing of in-process, bulk, and finished-product samples. Ensure appropriate status identification and segregation of materials/products. 5. GMP & Compliance Ensure compliance with cGMP, GDP, data integrity, SOPs, and applicable regulatory requirements. Conduct routine GMP observations and report gaps to the concerned department. Support implementation of corrective actions arising from audits and inspections. Participate in internal audits, self-inspections, customer audits, and regulatory inspections.

Job Details

Role Level: Mid-Level Work Type: Full-Time
Country: India City: Dholka ,Madhya Pradesh
Company Website: https://www.cadilapharma.com/ Job Function: General Management
Company Industry/
Sector:
Pharmaceutical Manufacturing

What We Offer

About the Company

Searching, interviewing and hiring are all part of the professional life. The TALENTMATE Portal idea is to fill and help professionals doing one of them by bringing together the requisites under One Roof. Whether you're hunting for your Next Job Opportunity or Looking for Potential Employers, we're here to lend you a Helping Hand.

Report

Disclaimer: talentmate.com is only a platform to bring jobseekers & employers together. Applicants are advised to research the bonafides of the prospective employer independently. We do NOT endorse any requests for money payments and strictly advice against sharing personal or bank related information. We also recommend you visit Security Advice for more information. If you suspect any fraud or malpractice, email us at abuse@talentmate.com.

Ready to Apply?

One-click apply with your Talentmate profile.

Job Snapshot

Work TypeFull-Time
Role LevelMid-Level
Job FunctionGeneral Management
CityDholka
IndustryPharmaceutical Manufacturing
Posted04 Nov 2026
Job ID2611-6430-1355
Recent Jobs
View More Jobs
Talentmate Instagram Talentmate Facebook Talentmate YouTube Talentmate LinkedIn