Executive (QC Micro) Jobs in Brawn Laboratories Limited - Faridabad, Haryana
2 - 3 Years of Experience
Not disclosed 
Full TimeBrawn Laboratories Limited
Faridabad, Haryana, India
Posted on 30-01-2026
1 Vacancy
Description
- Job Title: Executive (QC Micro)
- Qualification: MSc/BSc
- Location: Brawn Laboratories Limited - Faridabad, Haryana
- Work Experience: 2 to 3 Years
Job Description
- Perform routine microbiological testing on raw materials, in-process samples, and finished products.
- Conduct sterility tests, microbial limit tests, bioburden testing, and environmental monitoring.
- Prepare and maintain accurate laboratory records, SOPs, and test reports.
- Assist in investigating deviations and Out of Specification (OOS) results.
- Support the QA team during internal audits and inspections.
- Monitor cleanroom hygiene and lab safety protocols.
- Maintain and operate laboratory equipment as per SOPs.
- Participate in validation, calibration, and preventive maintenance activities.
- Follow cGMP / GLP / ISO standards in all testing activities.
- Coordinate with production and QA teams to ensure product quality.
- Maintain biohazard and chemical waste disposal protocols.
Take this opportunity to join Brawn Laboratories Limited - Faridabad, Haryana as a Executive (QC Micro) in Faridabad, Haryana and build a successful career in the healthcare industry. Apply today for this job opportunity and grow with a leading healthcare organization.
Category
Paramedical / Technician
Preferred Education
Key Skills
About Organization
Brawn Laboratories Limited, Faridabad, Haryana, is a well-established pharmaceutical manufacturing company known for its strong quality systems, compliance with regulatory standards, and commitment to producing safe and effective medicines. The organization is expanding its quality assurance function and invites applications from qualified QA professionals. The role involves reviewing and approving laboratory test results, ensuring compliance with GMP and internal SOPs, supporting stability studies, managing documentation and batch records, and coordinating with QC and production teams. Responsibilities also include handling deviations, OOS/OOT investigations with CAPA support, participation in internal audits, monitoring laboratory compliance, and contributing to continuous quality improvement initiatives. This opportunity offers hands-on exposure to regulated pharmaceutical operations, professional skill development, and long-term career growth in a structured, quality-driven manufacturing environment.
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