Quality Assurance injectables and formulations

Globion; Hyderabad; On-site; INR 420,000 - 700,000; Full time

Job summary

Virbac Biologicals Private Limited, located near Hyderabad in Genome Valley, is seeking a Quality Assurance professional with a focus on microbiology and sterility testing.

The candidate will conduct microbiological analyses, develop testing protocols, and ensure compliance with cGMP. Experience in BET and sterility methods, plus strong documentation skills, is required for successful product releases.

Qualifications

• 2–5 years of lab experience in the pharmaceutical industry.
• Strong knowledge of microbiology, BET and sterility testing.
• Familiarity with cGMP and QA processes.
• Ability to work independently.

Responsibilities

• Conduct microbiological tests on pharmaceutical products to ensure sterility and quality.
• Develop and implement test protocols for sterility testing.
• Maintain accurate records and documentation of test results.
• Collaborate with cross-functional teams on product development and release.

Skills

Microbiology

cGMP

Quality Assurance

Sterility testing

Job description

Company Name- Virbac Biologicals Private limited (Formerly Known as Globion India Pvt Ltd)

It is an Poultry manufacturing company

Location- Karkapatla Genome Valley 50 kms from Hyderabad

Department- Quality Assurance

Roles and Responsibilities :

• Conduct microbiological tests on pharmaceutical products to ensure sterility and quality.
• Develop and implement test protocols, procedures, and methods for sterility testing.
• Collaborate with cross-functional teams to resolve issues related to product development, manufacturing, and release.
• Maintain accurate records of test results, reports, and documentation.

Job Requirements :

• 2-5 years of experience in a laboratory setting within the pharmaceutical industry.
• Strong knowledge of microbiology principles, including bacterial endotoxin testing (BET) and sterility testing methods.
• Experience with quality assurance processes and regulations (e.g., cGMP).
• Ability to work independently with minimal supervision.