Job Summary
* Roles: Assistant Manager – Quality Assurance (IPQA) and Executive – Quality Assurance (IPQA).
* Industry: Leading Healthcare/Pharmaceuticals.
* Location: USFDA-Approved Facility, Daman.
* Experience Required: 6 to 11 years (depending on the role).
* Key Focus: Shopfloor IPQA, Process/Cleaning Validation, APQR, and Audit Readiness.
* Requirement: Mandatory experience in USFDA-approved OSD (Oral Solid Dosage) formulation sites.
Company Overview
USV Private Limited is a distinguished leader in the healthcare industry with a legacy spanning 63 years. As a top-ranked company in the Oral Anti-Diabetic segment, we maintain a robust global footprint across more than 65 countries. We are currently seeking highly skilled and dedicated Quality Assurance professionals to join our high-performance team at our state-of-the-art, USFDA-approved manufacturing facility located in Daman.
Position 1: Assistant Manager – IPQA
We are looking for an experienced QA leader to manage shopfloor operations and ensure strict regulatory compliance.
* Experience: 9 to 11 years in the pharmaceutical industry.
* Job Stability: Candidates must have a minimum of 2 years of service in their current organization.
* Essential Qualifications: Proven experience working in a USFDA-approved OSD formulation manufacturing environment is mandatory.
* Key Responsibilities:
* Oversight of shopfloor IPQA activities and real-time monitoring of manufacturing processes.
* Managing process and cleaning validation, including protocol development and execution.
* Leading the preparation of Annual Product Quality Reviews (APQR) and managing Continued Process Verification (CPV) activities.
* Ensuring ongoing regulatory compliance and maintaining high standards of audit readiness for global inspections.
Position 2: Executive – IPQA
We are looking for a detail-oriented QA professional to support our quality systems and shopfloor monitoring.
* Experience: 6 to 8 years in the pharmaceutical industry.
* Job Stability: Candidates must have a minimum of 2 years of service in their current organization.
* Essential Qualifications: Must have experience working at a USFDA-approved OSD formulation site.
* Key Responsibilities:
* Conducting shopfloor IPQA inspections and ensuring adherence to Standard Operating Procedures (SOPs).
* Providing real-time process monitoring to ensure product quality.
* Assisting in the preparation of APQR and supporting CPV-related tasks.
* Contributing to the overall maintenance of quality management systems within the production environment.
Why Join Us?
At USV Private Limited, we prioritize innovation, quality, and professional growth. Working at our Daman facility offers you the opportunity to operate within a globally recognized, USFDA-compliant environment. You will work alongside industry experts, gain exposure to international quality standards, and play a critical role in delivering life-saving healthcare products to patients worldwide. We foster a culture of excellence and value employees who are committed to precision and ethical manufacturing practices.
How to Apply
If you meet the above requirements and are ready to advance your career with a premier healthcare organization, we invite you to apply.
Please send your updated resume to: [email protected]
To ensure your application is processed efficiently, please use the following format in the email subject line:
[Position Name] – QA (Daman) | [Your Name]
Please ensure that your CV highlights your specific experience with USFDA-approved OSD formulation sites to help us expedite the review process. We look forward to reviewing your credentials and potentially welcoming you to our team as we continue to innovate in the healthcare space.
USV Private Limited is an equal opportunity employer committed to creating a diverse and inclusive workplace. We appreciate all applications; however, only those candidates whose qualifications align with our current requirements will be contacted for an interview.