Piramal Pharma Limited Walk-In Interviews for Multiple Positions on 26th July' 2026 - Pharmawisdom.co.in

Piramal Pharma Limited is conducting a Walk-in Interview for multiple Quality Control (QC), Quality Assurance (QA), and IPQA positions for its Pithampur (Indore), Madhya Pradesh manufacturing facility. This recruitment drive is aimed at experienced pharmaceutical professionals with expertise in analytical testing, quality assurance, validation, stability studies, and regulatory compliance. Interested candidates can attend the walk-in interview on 26th July 2026 in Chhatrapati Sambhajinagar (Aurangabad), Maharashtra.

About Piramal Pharma Limited

Piramal Pharma Limited is one of India’s leading global pharmaceutical companies, offering integrated solutions across contract development and manufacturing (CDMO), complex hospital generics, and consumer healthcare products. With world-class manufacturing facilities and a strong commitment to quality, innovation, and regulatory excellence, Piramal Pharma provides exceptional career opportunities for professionals in manufacturing, quality, research, and operations.

Job Overview

Particulars Details
Company Piramal Pharma Limited
Departments Quality Control (QC), Quality Assurance (QA), IPQA
Job Location Pithampur (Indore), Madhya Pradesh
Interview Location Chhatrapati Sambhajinagar (Aurangabad), Maharashtra
Employment Type Full-Time
Interview Date 26th July 2026

Open Positions

Position Qualification Experience Required
QC Executive / Sr. Executive B.Pharm / M.Sc. Minimum 3 Years
QC Manager – Method Validation / Transfer B.Pharm / M.Sc. Minimum 10 Years
QC Manager – Stability B.Pharm / M.Sc. Minimum 10 Years
Lab QA / QC Reviewer – Sr. Executive / Dy. Manager B.Pharm / M.Sc. Minimum 6 Years
IPQA Manager B.Pharm / M.Sc. Minimum 9 Years

Key Responsibilities

QC Executive / Sr. Executive

  • Perform analytical testing using HPLC, GC, LCMS, and Dissolution instruments.
  • Ensure accurate documentation and compliance with GMP and quality standards.
  • Support routine quality control activities for pharmaceutical products.

QC Manager – Method Validation / Transfer

  • Lead analytical method validation and method transfer activities.
  • Manage and mentor a team of 8–10 members.
  • Ensure compliance with regulatory guidelines and quality systems.

QC Manager – Stability

  • Manage end-to-end stability studies for Oral Solid Dosage (OSD) products.
  • Lead a team of 15–20 members.
  • Monitor stability protocols, documentation, and regulatory compliance.

Lab QA / QC Reviewer – Sr. Executive / Dy. Manager

  • Review analytical and electronic QC data.
  • Investigate and manage OOS (Out of Specification) and OOT (Out of Trend) events.
  • Ensure compliance with Quality Management System (QMS) requirements.

IPQA Manager

  • Lead In-Process Quality Assurance (IPQA) activities for the OSD manufacturing unit.
  • Ensure compliance with cGMP and regulatory requirements.
  • Supervise a team of 8–10 members and drive quality improvement initiatives.

Required Skills

  • HPLC
  • Gas Chromatography (GC)
  • LCMS
  • Dissolution Testing
  • Analytical Method Validation
  • Method Transfer
  • Stability Studies
  • Quality Control
  • Quality Assurance
  • In-Process Quality Assurance (IPQA)
  • OOS & OOT Investigation
  • cGMP Compliance
  • QMS
  • Regulatory Compliance
  • Team Leadership
  • Pharmaceutical Documentation

Walk-in Interview Details

Particulars Information
Interview Date Sunday, 26th July 2026
Reporting Time 9:00 AM – 3:00 PM
Interview Venue Lemon Tree Hotel, R-7/2, Chikalthana, Airport Road, Chhatrapati Sambhajinagar (Aurangabad) – 431001, Maharashtra
Job Location Pithampur (Indore), Madhya Pradesh

Documents to Carry

Candidates should carry:

  • Updated Resume/CV
  • Current Appointment Letter
  • Latest Salary Slip
  • Educational Certificates and Marksheets
  • Government-issued Photo ID Proof
  • Experience Certificates
  • Passport-size Photographs

Contact Information

Why Join Piramal Pharma?

  • Join one of India’s leading global pharmaceutical organizations.
  • Work with advanced analytical laboratories and world-class manufacturing facilities.
  • Gain exposure to quality systems, regulatory compliance, and leadership roles in pharmaceutical operations.
  • Excellent opportunities for career growth, learning, and professional development.
  • Be part of a company committed to innovation, quality, and excellence in pharmaceutical manufacturing.

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