QA- Officer / Sr. Officer(QA Lab) 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: QA- Officer / Sr.Officer(QA Lab)
- Qualification: BPharm
- Location: Brawn Laboratories Limited - Faridabad, Haryana
- Work Experience: 2 to 3 Years
Job Description
- Implement and maintain QA policies, SOPs, and compliance standards in the laboratory.
- Review and approve batch manufacturing records, QC test reports, and analytical data.
- Ensure proper documentation of deviations, non-conformances, and investigations.
- Monitor lab operations for adherence to GMP/GLP guidelines.
- Conduct internal audits and assist in regulatory inspections.
- Perform root cause analysis and implement CAPA for quality issues.
- Ensure equipment calibration, validation, and maintenance.
- Coordinate with QC and production teams for smooth workflow.
- Prepare and maintain quality reports and metrics.
- Provide training and guidance to junior QA/QC staff.
- Ensure regulatory compliance with national and international guidelines.
- Support continuous improvement initiatives in quality processes.
Take this opportunity to join Brawn Laboratories Limited - Faridabad, Haryana as a QA- Officer / Sr. Officer (QA Lab) 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 Assurance (QA)
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.
Aggregated job.
Learn more