Executive/ Sr. Executive For Vaccines Manufacturing

Reliance Life Sciences; Mumbai, Navi Mumbai; On-site; INR 800,000 - 1,100,000; Full time

Job summary

Reliance Lifesciences is seeking an Executive/Sr. Executive for vaccines manufacturing based in Navi Mumbai/Mumbai. The role requires 4–5 years of hands-on experience in GMP vaccine production and familiarity with media preparation, aseptic transfers, and batch records.

The ideal candidate will perform environmental monitoring, CIP/SIP operations, and in-process testing, ensuring compliance with GMP and QA review timelines.

Qualifications

• 4–5 years of experience in vaccine manufacturing or related bioprocessing roles.
• Qualification in Biotechnology or Microbiology with relevance to GMP facilities.
• Experience with batch records, GMP documentation and cleanroom protocols.

Responsibilities

• Prepare media and inoculum for vaccine manufacturing processes.
• Conduct environmental monitoring in controlled production areas.
• Execute harvest inactivation and aseptic transfers per GMP guidelines.
• Operate CIP/SIP for production vessels and maintain clean utilities.
• Perform aseptic filtration and in-process sterility testing during production.
• Ensure proper inactivation and transfers to secondary containers under sterile conditions.
• Maintain and complete BMR and other GMP documentation.
• Record daily production activities and submit BMR to QA in a timely manner.

Skills

GMP compliance

Aseptic technique

Documentation

Quality control

Education

M.Sc in Biotechnology

B.Tech in Biotechnology

M.Tech in Biotechnology

M.Sc in Microbiology

Tools

CIP/SIP systems

Environmental monitoring equipment

Job description

We at Reliance Lifesciences are looking to hire a Executive/ Sr. Executive for Vaccines Manufacturing with 4 to 5 years of experience.

Location: Navi Mumbai/ Mumbai

Reliance Life Sciences

Qualification: M.Sc/B.Tech/M.Tech in Biotechnology/Microbiology

KEY RESPONSIBILITIES

• 1. Perform media and inoculum preparation for vaccine manufacturing processes.
• 2. Conduct environmental monitoring in controlled production areas.
• 3. Execute harvest inactivation and aseptic transfer operations as per GMP guidelines
• 4. Operate CIP (Cleaning in Place) and SIP (Sterilization in Place) of production vessels.
• 5. Perform aseptic filtration and In process sterility testing during production stages.
• 6. Perform inactivation and aseptic transfer to secondary containers under sterile condition.
• 7. Maintain and completed BMR (Batch Manufacturing Records) and other GMP documentation.
• 8. Record daily production activities and ensured timely review and submission of BMR to QA.