Executive Associate – Production Mammalian

Lupin; Pune District; On-site; INR 420,000 - 620,000; Full time

Job summary

Lupin in Pune District, Maharashtra, is seeking a Biotechnology graduate with 2-5 years of experience for production operations support. The role covers buffer prep, CIP/SIP for chromatography, and coordination with QC/QA teams to ensure GMP-compliant processes.

Responsibilities include maintaining SOPs and BPRs, material inventory, autoclave operation, and deviation management, contributing to overall facility performance.

Qualifications

• 2-5 years of experience in biotechnology operations.
• Graduation in Biotechnology.

Responsibilities

• Buffer preparation for small and large-scale operations, IPQC operation of buffer and protein intermediate samples.
• CIP of chromatography systems, TFF systems and process vessels.
• SIP of TFF systems and process vessels.
• Operation of chromatography systems, TFF systems, Virus Filtration System, DS filtration for protein purification.
• Preparation, execution and maintenance of SOP’s, BPRs, qualification documents and other facility related documents.
• Co- ordinate with QC/QA teams on day-to-day activities of production operations.
• Review of executed BPR’s.
• Raw material and consumables inventory planning and maintenance.
• Operation, maintenance of sterile and decontamination autoclave.
• Deviation identification, initiation and investigation assistance for the facility related deviations.

Skills

IPQC operation

Buffer preparation

GMP documentation

Education

Graduation in Biotechnology

Tools

Chromatography systems

TFF systems

Virus Filtration System

DS filtration

Job description

• Date: Oct 12, 2026
• Company: Lupin

Job Description

• Buffer preparation for small and large-scale operations, IPQC operation of buffer and protein intermediate samples.
• CIP of chromatography systems, TFF systems and process vessels.
• SIP of TFF systems and process vessels.
• Operation of chromatography systems, TFF systems, Virus Filtration System, DS filtration for protein purification.
• Preparation, execution and maintenance of SOP’s, BPRs, qualification documents and other facility related documents.
• Co-ordinate with QC/QA teams on day-to-day activities of production operations.
• Review of executed BPR’s.
• Raw material and consumables inventory planning and maintenance.
• Operation, maintenance of sterile and decontamination autoclave.
• Deviation identification, initiation and investigation assistance for the facility related deviations.

Additional Job Responsibilities:

• Routine monitoring of facility and record maintenance e.g. temperature, humidity, differential pressure.
• Overall housekeeping management.
• To assist in facility validation in coordination with QA.

Work Experience

2-5 years of experience

Education

Graduation in Biotechnology or Biotechnology

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