Sr. Officer (QC Micro) Jobs in Brawn Laboratories Limited - Faridabad, Haryana

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Sr. Officer (QC Micro) Jobs in Brawn Laboratories Limited - Faridabad, Haryana

work outline icon2 - 3 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Brawn Laboratories Limited

time outline iconFaridabad, Haryana, India

Posted on 30-01-2026

1 Vacancy

Description

  1. Job Title: Sr. Officer (QC Micro)
  2. Qualification: MSc/BSc
  3. Location: Brawn Laboratories Limited - Faridabad, Haryana
  4. Work Experience: 2 to 3 Years

Job Description

  1. Conduct microbiological testing of raw materials, in-process samples, and finished products.
  2. Perform sterility testing, microbial limit tests, bioburden testing, and environmental monitoring.
  3. Ensure compliance with cGMP, GLP, and other regulatory guidelines.
  4. Prepare and maintain accurate QC microbiology documentation and reports.
  5. Investigate and document microbiological deviations / OOS (Out of Specification) results.
  6. Monitor cleanroom environments and hygiene standards.
  7. Ensure proper calibration and maintenance of microbiology lab instruments.
  8. Support validation and qualification activities of lab equipment.
  9. Assist QA team during audits and regulatory inspections.
  10. Train and guide junior QC microbiologists and lab technicians.
  11. Ensure proper handling and disposal of biological / microbial waste.
  12. Participate in continuous improvement initiatives in QC processes.

Take this opportunity to join Brawn Laboratories Limited - Faridabad, Haryana as a Sr.Officer (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

Pharmaceuticals

Functional Area

Pharma Quality Control (QC)

Preferred Education

BSc MicrobiologyMSc Microbiology

Key Skills

Coordination SkillsTeamworkAttention to DetailDocumentation

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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