India's DMPLOI - Jobs & Networking AppIpca Laboratories Limited, one of India’s leading pharmaceutical companies, has announced a Walk-In Interview Drive for Freshers at its Indore facility. This recruitment is aimed at candidates looking to start their careers in the pharmaceutical manufacturing sector. The positions are available on a third-party contract roll basis for immediate joiners.
The company is hiring for multiple departments, including PPA/Production (API) Technician, EHS (Fire & Safety), and PPA/Production (API) Chemist. Candidates with qualifications ranging from 12th Pass, B.Sc., Diploma, and B.Tech in Fire & Safety are encouraged to attend the interview.
Overview of the Walk-In Drive
Particulars Details
Company Name
Ipca Laboratories Limited
Job Type
Contract Roll (Third Party)
Location
Indore, Madhya Pradesh
Interview Date
20 June 2026
Interview Time
11:00 AM to 3:00 PM
Gender
Male Candidates
Joining
Immediate Joiners Preferred
Open Positions
1. PPA/Production (API) Technician
Qualification: 12th Pass
Key Responsibilities:
Support API production planning and manufacturing activities.
Maintain production records and batch documentation.
Coordinate with different departments for smooth operations.
Follow GMP and safety guidelines.
Monitor production processes and equipment.
2. EHS (Fire & Safety)
Qualification: Diploma/B.Tech in Fire & Safety
Key Responsibilities:
Assist in environmental, health, and safety activities.
Conduct fire safety inspections and audits.
Support employee safety training programs.
Participate in emergency preparedness activities.
Maintain EHS documentation and compliance records.
3. PPA/Production (API) Chemist
Qualification: B.Sc.
Key Responsibilities:
Perform batch charging and process operations.
Handle reactors, centrifuges, ANFDs, and RCVDs.
Maintain accurate production documentation.
Ensure compliance with GMP and safety standards.
Monitor manufacturing processes and product quality.
Why Join Ipca Laboratories?
Ipca Laboratories is a globally recognized pharmaceutical company known for its strong presence in APIs and finished dosage formulations. Working with Ipca offers:
Exposure to advanced pharmaceutical manufacturing processes.
Hands-on experience with API production equipment.
Learning opportunities in GMP-regulated environments.
Career growth within the pharmaceutical industry.
Experience in safety and compliance-driven operations.
Documents to Carry
Candidates attending the walk-in interview should bring:
Updated Resume/CV
Educational Certificates
Government Photo ID Proof
Passport Size Photographs
Experience Documents (if applicable)
Recent Salary Documents (if any)
Contact Information
Email: abhishekd.parmar@ipca.com
Note: Ipca Laboratories does not charge any fee at any stage of the recruitment process. Candidates should avoid dealing with unauthorized agencies or individuals claiming recruitment charges.
Technical FAQs
1. What is GMP and why is it important in API manufacturing?
GMP (Good Manufacturing Practices) ensures pharmaceutical products are consistently produced and controlled according to quality standards. It minimizes contamination risks, documentation errors, and quality deviations.
2. What is the function of a reactor in API production?
A reactor is used to carry out chemical reactions under controlled conditions such as temperature, pressure, and agitation during API manufacturing processes.
3. What are ANFD and RCVD equipment used for?
ANFD (Agitated Nutsche Filter Dryer) is used for filtration and drying of pharmaceutical products, while RCVD (Rotary Cone Vacuum Dryer) is used to dry sensitive materials under vacuum conditions.
4. What are the key responsibilities of an EHS professional in a pharmaceutical plant?
EHS professionals ensure workplace safety, conduct risk assessments, manage fire protection systems, provide safety training, and ensure compliance with environmental and safety regulations.
5. Why is batch documentation critical in pharmaceutical manufacturing?
Batch documentation provides complete traceability of production activities, supports regulatory compliance, helps during audits, and ensures product quality and patient safety.
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