IPCA Laboratories Mega Walk-In Drive API & Formulation Roles in Production, QA, QC, and R&D

IPCA Laboratories, a leading, fully integrated Indian pharmaceutical company with world-class, USFDA-approved manufacturing facilities, is conducting a large-scale walk-in interview event. The drive aims to recruit experienced professionals for its Sejawta, Ratlam unit.

The company is particularly looking for candidates with experience in WHO, MHRA, or USFDA-approved Pharmaceutical API and Formulation plants.

Walk-In Interview Details

The interviews will be held in Indore:

Date: Sunday, 16th November 2025
Time: 11:00 hrs to 16:00 hrs
Venue: Ipca Laboratories Limited, Pologround, Indore
Alternative: Candidates unable to attend may share their resumes via email to hrd.ratlam@ipca.com.

Detailed Job Roles and Requirements

Roles are open for Chemist, Officer, Senior Officer, and Executive levels.

1. Production (Formulation – Injection)

Qualification & Experience: B.Sc / M.Sc / B.Pharm / M.Pharm / ITI, with 2 to 10 years of experience.
Focus: Must have experience in Sterile area manufacturing (Ampoule and Vial), Shift supervision, and thorough knowledge of OOS, OOT, CAPA, and online documentation as per SOP/BMR. Requires expertise with equipment like Autoclave, Washing, Filling and Sealing Machines, media preparation, media filling, and 2D serialization.

2. Production (Formulation – Tablet)

Qualification & Experience: B.Sc / M.Sc / B.Pharm / M.Pharm, with 4 to 8 years of experience.
Focus: Experience operating Tablet Manufacturing machines (Granulation, Compression, Coating) and dispensing raw materials. Must be proficient in handling batch record documentation (BMR, BPR, E-Log Book). Knowledge of Primary Packing machines (Blister Packing, Cartonater, 2D Printing) and Secondary Packing machines (BQS, Elmac, Strip Machine, Track & Trace Machine) is required.

3. Quality Assurance (Formulation)

Qualification & Experience: B.Sc / M.Sc / B.Pharm / M.Pharm, with 4 to 8 years of experience.
Focus: Expertise in IPQA (Sterile & Non-Sterile), Qualification (Sterile), Validation (Sterile), Analytical QA, and Stability Studies. Must have exposure to QMS (Deviation, CAPA, etc.) utilizing the Trackwise system, OOS investigation (Microbiological), Risk Assessment, and Market Complaint handling.

4. Production (API)

Qualification & Experience: B.Sc / M.Sc / Diploma Chemical / B.Tech Chemical / ITI, with 2 to 10 years of experience.
Focus: Experience in the powder processing area, Batch Planning, and Manpower Handling. Requires hands-on experience with equipment such as Reactors, GMP, Filters, Centrifugation, GLR, Dryer, FBD, RCVD, VTD, STD, JET MILL, MULTI MILL, BLENDER, SHIFTER, and performing unit operations strictly as per BPR.

5. Quality Control (API)

Qualification & Experience: B.Sc / B.Pharm, with 2 to 10 years of experience.
Focus: Seeking Analyst/Reviewer for Wet lab/Stability/Inprocess Lab & Micro lab. Requires analytical expertise in HPLC/GC/LCMS/GCMS operations and classic instruments (UV, Autotitrator, IR, Karlfisher, pH meter). Also includes Micro-related testing like Sterility Test Validation, MLT (Microbiological Limit Test), Reconciliation, and Environmental/Water Analysis.

6. PCE Lab (R&D)

Qualification & Experience: M.Sc / B.Pharm / M.Pharm, with 4 to 10 years of experience.
Focus: To perform, supervise, and review analysis for Process optimization, cost reduction, and Trouble Shooting experiments. Provide technical inputs for OOS/OOT/deviation/market complaint investigations. Involve in scale-up (lab to pilot/commercial) and analytical method transfer to IPQC/QC.

7. Engineering (API)

Qualification & Experience: BE/B.Tech/Diploma (Mechanical/Electrical/Instrumentation/Civil), with 4 to 10 years of experience.
Focus: Experience in mechanical & electrical breakdown and troubleshooting, routine maintenance of API equipment (Reactors, Filters, Centrifugation). Knowledge of Engineering Pharma Projects (Civil/Mechanical) and Documentation (DQ, IQ, OQ) is required, with preference given to candidates who have faced USFDA and other audits.