Executive - Production Mammalian

Lupin; Pune District; On-site; INR 600,000 - 900,000; Full time

Job summary

Lupin in Pune is seeking a Shift Supervisor for the downstream team to lead, train, and mentor staff in buffer prep, IPQC sampling, and chromatography operations. You will ensure CIP/SIP, maintain SOPs, and coordinate with QC/QA for daily production tasks.

The role emphasizes strict GMP adherence and continuous improvement across processing steps. Ideal candidates have 4-8 years of related experience and a biotech background (B.Tech or PG in Biotechnology).

Qualifications

• 4-8 years of relevant experience in biopharma manufacturing.

Responsibilities

• Act as shift supervisor, lead, train and mentor the downstream team.
• 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.
• Monitor key process parameters.
• Prepare, execute and maintain SOPs, BPRs, qualification documents and other facility related documents.
• Coordinate with QC/QA teams on day-to-day activities of production operations.
• Review of executed BPRs.
• Raw material and consumables inventory planning and maintenance.
• Operation, maintenance of sterile and decontamination autoclave.
• Deviation identification, initiation and investigation assistance for facility related deviations.
• Preparation of GMP documents like- Qualification and validation protocols and other process or facility related documents for media preparation and cell culture operations.

Skills

Result Orientation

Strategic Agility

Customer Centricity

Education

B.Tech in Biotechnology

Post Graduation in Biotechnology

Job description

• Act as shift supervisor, lead, train and mentor the downstream team.
• 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.
• Monitor key process parameters.
• 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.
• Preparation of GMP documents like- Qualification and validation protocols and other process or facility related documents for media preparation and cell culture operations.

Work Experience

4-8 years of relavant experience.

Education

B.Tech in Biotechnology or Biotechnology

Post Graduation in Biotechnology or Biotechnology

5. Result Orientation

1. Strategic Agility

3. Customer Centricity

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