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  • Ipca Laboratories Organizes Mega Walk-in Interview in Indore for Dewas API & Pithampur Injectable Units: Openings in Production, Technology Transfer, DP Manufacturing, and QC
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Ipca Laboratories Organizes Mega Walk-in Interview in Indore for Dewas API & Pithampur Injectable Units: Openings in Production, Technology Transfer, DP Manufacturing, and QC

Pharm'Up 3 min read

Ipca Laboratories Limited—a globally integrated pharmaceutical leader with over 60 years of presence across 120+ countries, supplying over 350 formulations and 80 APIs with regulatory clearances from the UK-MHRA, EDQM, and WHO-Geneva—has announced a comprehensive walk-in recruitment drive in Indore, Madhya Pradesh.

The interview session is scheduled for Sunday, September 27, 2026, targeting qualified professionals in chemical engineering, chemistry, pharmacy, microbiology, and biotechnology for diverse roles across its Dewas API manufacturing site and the Pithampur Bio-Manufacturing (Sterile/Injectable) facility.

Dewas API Unit Opportunities

1. Production API

  • Designations: Officer / Chemist / Technician
  • Educational Background: Diploma / B.E. / B.Tech in Chemical Engineering, or B.Sc. in Chemistry
  • Experience Required: 2 to 7 years
  • Core Responsibilities:
    • API batch manufacturing, synthesis operations, and shift supervision.
    • Operation and monitoring of process equipment including chemical reactors, centrifuges, distillation setups, and filtration units.
    • Accurate real-time documentation and completion of Batch Manufacturing Records (BMR) and Batch Cleaning & Packing Records (BCPR).

2. Continuous Process & Technology Transfer

  • Designation: Officer
  • Educational Background: B.E. / B.Tech in Chemical Engineering
  • Experience Required: 2 to 5 years
  • Core Responsibilities:
    • Process engineering, pilot plant operations, batch scale-up, and technical transfer workflows.
    • Direct hands-on expertise in flow chemistry platforms and continuous manufacturing systems.

Pithampur Bio-Manufacturing Unit Opportunities (Sterile / Injectables)

1. Drug Product (DP) Manufacturing

  • Assistant Manager (9–13 Years Experience):
    • Qualification: B.Pharm / M.Pharm
    • Key Scope: Audit readiness, global regulatory inspection compliance, QMS handling and investigations (Deviations, Incident Management, Change Control, CAPA), SOP authoring, and log review.
  • Executive / Senior Executive (6–9 Years Experience):
    • Qualification: B.Pharm / M.Pharm
    • Key Scope: Aseptic shop-floor monitoring, core batch execution, aseptic assurance protocols, and facility/equipment qualification and validation in DP sterile areas.
  • Officer (2–5 Years Experience):
    • Qualification: B.Pharm / M.Pharm
    • Key Scope: Autoclave operations, terminal sterilization/aseptic preparation, injectable batch manufacturing, and related floor documentation.

2. Quality Control (Sterile / Injectable)

  • Executive – Microbiology (5–9 Years Experience):
    • Qualification: M.Sc. in Microbiology
    • Key Scope: Supervision of sterility testing, Bacterial Endotoxin Testing (BET), bioburden monitoring, water system evaluation, analytical record review, and failure investigations (OOS/OOT).
  • Executive – QMS (5–9 Years Experience):
    • Qualification: Post Graduate in Biotechnology or Microbiology
    • Key Scope: Handling electronic QMS modules, logging and investigating deviations, executing CAPA plans, and leading Quality Risk Management (QRM) assessments.
  • Executive – Bioassay (5–7 Years Experience):
    • Qualification: M.Sc. / B.Tech in Biotechnology or Biochemistry
    • Key Scope: Carrying out bioassay testing protocols for finished drug products and ongoing stability program samples.
  • Officer – Biochemistry (2–5 Years Experience):
    • Qualification: M.Sc. / B.Tech in Biotechnology or Biochemistry
    • Key Scope: Wet lab analysis and biochemical testing of in-process stages, finished batches, and stability study samples.
  • Officer – Raw Materials & Packaging Materials (RM/PM) (2–5 Years Experience):
    • Qualification: M.Sc.
    • Key Scope: Verification and processing of Goods Inward Movement (GIM) for RM/PM, analytical sampling and status labeling, routine operation of Karl Fischer (KF) titrators, autotitrators, Total Organic Carbon (TOC) analyzers, and analytical balances.

Walk-in Interview Schedule & Location

  • Date: September 27, 2026 (Sunday)
  • Time: 09:00 AM to 05:00 PM (09:00 to 17:00 hrs)
  • Venue:Papaya Tree Hotel,A.B. Road, Rau Bypass Square,Opposite Dr. Hardia Eye Hospital,Indore, Madhya Pradesh

Direct Contact for Queries

  • Dewas API: Mr. Gautam Anand — gautam.anand@ipca.com
  • Pithampur Bio-Mfg.: Ms. Geetanjali Sahu — geetanjali.sahu@ipca.com

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