
DRA (Drug Regulatory Affairs)-Officer Jobs in Brawn Laboratories Limited - Faridabad, Haryana
Brawn Laboratories Limited
Faridabad, Haryana, India
Posted on 30-01-2026
1 Vacancy
Description
- Job Title: DRA (Drug Regulatory Affairs)-Officer
- Qualification: MPharm/BPharm
- Location: Brawn Laboratories Limited - Faridabad, Haryana
- Work Experience: 1 to 2 Years
Job Description
- Prepare, review, and submit regulatory dossiers for drug approvals.
- Ensure compliance with national and international regulatory guidelines (CDSCO, USFDA, EMA).
- Maintain and update regulatory submission records and correspondence.
- Monitor approval timelines and follow-up with regulatory authorities.
- Assist in drug license applications, renewals, and amendments.
- Support clinical trial applications and post-marketing regulatory submissions.
- Coordinate with R&D, QA, Production, and Marketing teams for regulatory compliance.
- Maintain SOPs, guidelines, and regulatory documentation.
- Track changes in regulations and update the team accordingly.
- Assist in regulatory audits and inspections.
- Ensure labeling, packaging, and promotional material compliance.
Take this opportunity to join Brawn Laboratories Limited - Faridabad, Haryana as a DRA (Drug Regulatory Affairs)-Officer 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
Regulatory Affairs / Pharmacovigilance
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