Scientist / Sr Scientist - Microbiologist (Pharma)

Vimta Labs Ltd.; Shamirpet mandal; On-site; INR 600,000 - 900,000; Full time

Job summary

Vimta Labs Ltd. in Hyderabad (Shamirpet) is seeking a Microbiologist with 2–5 years in pharma QC. You will perform MLT, BET and sterility testing on materials and finished products, and monitor environmental conditions in cleanrooms.

The role covers validations and strict GMP/quality systems compliance, including LIMS data entry and deviation tracking. The ideal candidate holds an MSc in Microbiology/Biotech or BPharm/MPharm, with knowledge of USP/IP/EP pharmacopoeias and aseptic techniques.

Qualifications

• 2–5 years of pharma QC/analytical microbiology experience.
• MSc in Microbiology/Biotech or BPharm/MPharm.
• Knowledge of USP/IP/EP pharmacopoeias and GMP basics.

Responsibilities

• Perform routine Microbial Limit Testing (MLT), BET, and Sterility Testing on materials and products.
• Conduct Environmental Monitoring including air, surface and water sampling in cleanrooms.
• Assist in MLT validation, Method Validation, and Growth Promotion Testing.
• Maintain compliance with cGMP, GDP, and ISO 17025; manage LIMS entries and track deviations.

Skills

MLT

BET

Environmental Monitoring

Aseptic techniques

Education

M.Sc. Microbiology/Biotech

B.Pharm/M.Pharm

Tools

LIMS

Autoclave

Biosafety cabinet

Job description

Job Opening: Microbiologist

Location: Hyderabad (Shamirpet)

Experience: 2 to 5 years in Pharma QC/Analytical Microbiology
Education: M.Sc. (Microbiology/Biotech) or B.Pharm/M.Pharm

Responsibilities

• Microbial Testing: Perform routine Microbial Limit Testing (MLT), Bacterial Endotoxin Testing (BET), and Sterility Testing on raw materials and finished products.
• Environmental Monitoring (EM): Conduct air, surface, and water sampling within classified cleanrooms (Grade AD).
• Validations: Assist in MLT validation, Method Validation, and Growth Promotion Testing (GPT).
• Compliance: Maintain strict adherence to cGMP, Good Documentation Practices (GDP), and ISO 17025 guidelines. Handle LIMS data entries and track laboratory deviations/OOS.

Key Skills Required

• Hands-on experience with MLT, BET, and EM protocols in a pharma lab.
• Strong knowledge of global pharmacopoeias (USP, IP, EP).
• Expertise in aseptic techniques, handling autoclaves, biosafety hoods, and culture maintenance.