Brawn Laboratories is Hiring: Experienced Quality Assurance Professionals in Faridabad
About Brawn Laboratories:
Brawn Laboratories is a leading name in the pharmaceutical manufacturing sector, dedicated to producing high-quality healthcare products. We are committed to maintaining the highest standards of quality assurance and regulatory compliance across all our operations. As we continue to grow, we are expanding our talented Quality Assurance team.
The Opportunity:
We are seeking dedicated and experienced QA professionals to join us at our facility in Faridabad. If you have a strong background in pharmaceutical Quality Assurance and are ready to contribute to a dynamic and compliant manufacturing environment, we invite you to explore the following exciting opportunities:
1. QA Sr. Executive / Assistant Manager
- Experience: 4+ years in pharmaceutical Quality Assurance.
- Key Responsibilities:
- Manage Vendor Qualification and conduct Vendor Audits to ensure compliance.
- Oversee and manage CAPA (Corrective and Preventive Actions), Deviation, and Change Control systems.
- Perform comprehensive reviews of Process Validation (PV), Batch Manufacturing Records (BMR), and Batch Packing Records (BPR).
- Ensure robust Quality Management System (QMS) implementation and meticulous documentation practices.
- Handle COPP (Certificate of Pharmaceutical Product) and Dossier Documentation.
2. QA Reviewer – Executive / Sr. Executive
- Experience: 3+ years in pharmaceutical Quality Assurance.
- Key Responsibilities:
- Lead the preparation, thorough review, and final approval of Process Validation documentation.
- Manage the preparation, review, and approval processes for BMR/BPR.
- Conduct comprehensive Quality & Quantity (Q&Q) and Bill of Material (BOM) reviews.
- Contribute significantly to COPP and Dossier Documentation efforts.
3. Sr. Executive – QA
- Experience: 4+ years in pharmaceutical Quality Assurance.
- Key Responsibilities:
- Drive Process Validation activities, including preparation, rigorous review, and ultimate approval.
- Oversee BMR/BPR preparation, review, and approval to ensure accuracy and compliance.
- Execute Dossier Data Review and assist with Drug Regulatory Authority (DRA) Submissions.
- Demonstrate strong leadership and project management skills by individually handling and managing a team.
Mandatory Requirement for All Positions:
Candidates must possess prior, demonstrable experience within the Pharma Manufacturing industry.
Location:
Faridabad
How to Apply:
Interested and qualified candidates are encouraged to apply by calling or sending a WhatsApp message to: 9319995661. Please clearly mention the position you are applying for in your communication.
