Introduction

Ipca Laboratories Limited, one of India’s leading pharmaceutical companies, has announced a Walk-In Interview for experienced professionals in its Bio-Manufacturing Division at Pithampur, Madhya Pradesh. The recruitment drive is focused on candidates with experience in Biotech and Biosimilar Manufacturing across Drug Substance Manufacturing, Drug Product Manufacturing, Engineering & Maintenance, Quality Assurance, Quality Control, and Mammalian Pilot operations.

This hiring initiative provides an excellent opportunity for qualified professionals seeking career growth in the biotechnology and pharmaceutical manufacturing industry.

Walk-In Interview Details

Company: Ipca Laboratories Limited (Bio-Manufacturing)

Location: Pithampur, Madhya Pradesh

Interview Date: 23rd August 2026 (Sunday)

Walk-In Time: 8:30 AM to 4:00 PM

Interview Venue: Hotel Enrise (By Sayaji), Survey No. 80/1, Phase-2, Marunji Road, Vinode Nagar, Wakad, Hinjewadi, Pimpri-Chinchwad, Pune, Maharashtra

Department-Wise Vacancies

1. Drug Substance Manufacturing

Downstream Processing Executive / Sr. Executive

Qualification:

M.Sc.

M.Tech.

B.Tech. in Biotechnology or Biochemistry

Experience Required: 5–9 Years

Key Skills:

Downstream processing

TFF Systems

Buffer preparation

Change Control

Deviation Handling

CAPA

OOS & OOT investigations

Upstream Processing Executive / Sr. Executive

Qualification:

M.Sc.

M.Tech.

B.Tech. in Biotechnology or Biochemistry

Experience Required: 5–9 Years

Key Skills:

Seed propagation

Media preparation

Bioreactor operations

Vial revival

Upstream manufacturing process

QMS documentation

2. Drug Product Manufacturing

Aseptic Technician

Qualification:

ITI

Diploma Mechanical

Diploma Chemical

Fitter Trade

Experience Required: 2–6 Years

Key Skills:

Vial labeling machine operation

PFS labeling machine handling

Troubleshooting

Aseptic shop-floor management

3. Engineering & Maintenance

Instrumentation & Automation Assistant Manager

Qualification:

B.E./B.Tech in E&C Engineering

Experience Required: 7–12 Years

Key Skills:

PLC Programming

SCADA Systems

Process automation

Equipment troubleshooting

Autoclave systems

Chromatography systems

TFF and Filling operations

Instrumentation & Automation / Process Maintenance Technician

Qualification:

ITI

Diploma Mechanical

Diploma E&C Engineering

Experience Required: 2–6 Years

Key Skills:

Preventive maintenance

Breakdown maintenance

Mechanical equipment handling

Shift maintenance operations

4. Quality Assurance (QA)

IPQA Executive / Sr. Executive

Qualification:

PG in Biotechnology

Microbiology

B.Pharm

Experience Required: 5–9 Years

Key Skills:

In-Process Quality Assurance

Vendor Qualification

Process Validation

Cleaning Validation

GMP Compliance

5. Quality Control (QC)

Bioassay / Biochemistry / QMS Executive / Sr. Executive

Qualification:

M.Sc.

M.Tech.

B.Tech Biotechnology

Biochemistry

Experience Required: 5–9 Years

Key Skills:

Bioassay Testing

Host Cell Protein (HCP)

Host Cell DNA (HCD)

Bioprocess Analysis

Impurity Profiling

Quality Management Systems

6. Mammalian Pilot

Assistant Manager / Executive

Qualification:

B.Tech

M.Tech

M.Sc Biotechnology

Microbiology

Biochemistry

Experience Required: 5–12 Years

Key Skills:

Upstream Processing

Downstream Processing

Quality Control

Quality Assurance

Engineering Operations

Important Eligibility Criteria

Only candidates with Biotech/Biosimilar Manufacturing Experience will be considered.

Candidates must possess relevant educational qualifications and industry experience.

Strong understanding of GMP, QMS, Validation, and Manufacturing Processes is preferred.

Documents Required

Candidates should carry the following documents:

Updated Resume

Passport Size Photographs

Aadhaar Card / Passport

Birth Certificate

10th Pass Certificate

Highest Qualification Certificates

Current Company Appointment Letter

Current Company CTC Proof

Last 3 Months Salary Slips

Relieving & Experience Letters from Previous Employers

PAN Card

UAN Number Details

Why Join Ipca Laboratories?

Career opportunities in advanced Bio-Manufacturing

Exposure to Biosimilar and Biotechnology operations

Professional growth in regulated pharmaceutical environments

Work with experienced industry professionals

Strong quality and compliance-driven culture

Technical FAQs

1. What is the difference between Upstream and Downstream Processing in Biopharmaceutical Manufacturing?

Upstream Processing involves cell culture development, media preparation, inoculum preparation, and bioreactor operations.

Downstream Processing focuses on purification, filtration, chromatography, concentration, and final product recovery after cell cultivation.

2. What is TFF (Tangential Flow Filtration) and why is it important?

TFF is a membrane filtration technology used for concentration, diafiltration, and purification of biological products. It improves product recovery, reduces processing time, and maintains product quality in biopharmaceutical manufacturing.

3. What are CAPA, OOS, and OOT in Quality Management Systems?

CAPA: Corrective and Preventive Action

OOS: Out of Specification Results

OOT: Out of Trend Results

These systems help pharmaceutical companies investigate deviations, identify root causes, and maintain regulatory compliance.

4. Why is PLC and SCADA knowledge important in pharmaceutical manufacturing?

PLC and SCADA systems automate production equipment and monitor manufacturing processes in real time. They improve operational efficiency, reduce human errors, and ensure compliance with GMP requirements.

5. What is IPQA and how does it support GMP compliance?

In-Process Quality Assurance (IPQA) monitors manufacturing activities during production. It verifies process compliance, documentation accuracy, cleanliness standards, and adherence to GMP guidelines to ensure consistent product quality.

Conclusion

The Ipca Laboratories Walk-In Interview 2026 offers excellent career opportunities for experienced biotechnology, biosimilar manufacturing, engineering, quality assurance, and quality control professionals. Candidates meeting the eligibility criteria should attend the interview with all required documents and take advantage of this opportunity to build a rewarding career in the pharmaceutical and biotechnology sector.