USV Hiring Quality Assurance – QMS (Formulation)
- About USV Pvt. Ltd.
- Role Overview: QA – QMS (Formulation)
- Department: Quality Assurance
- Section: QMS (Formulation)
- Designation: Assistant Manager / Deputy Manager
- Experience: 10–14 Years
- Qualification: B Pharm / M.Pharm / MSc
- Location: Daman
- Key Responsibilities
- H2: Regulatory & QMS Responsibilities
- H3: Audit & Compliance
- Desired Candidate Profile
- Why Join USV?
- Application Process
- Summary Table
B Pharm/M.Pharm QA Jobs in Daman – 10–14 Years Experience in Formulation QMS
Apply now for QA Manager Jobs at USV Pvt Ltd in Daman. Openings for B Pharm/M.Pharm/MSc graduates with 10–14 years’ experience in Formulation QMS.
Advance Your QA Career in Pharma – Join USV Private Limited, Daman
Are you an experienced pharma professional specializing in Quality Assurance (QMS)? USV Pvt. Ltd., a trusted name in the pharmaceutical sector, is inviting applications for the role of Assistant Manager / Deputy Manager – QA (QMS – Formulation) at its state-of-the-art manufacturing facility in Daman. This position is ideal for professionals with 10 to 14 years of in-depth QA experience who are looking for leadership opportunities and to work in a globally compliant GMP environment.
This opportunity is ideal for graduates from B Pharm, M.Pharm, or MSc backgrounds with a passion for compliance, documentation, and audit preparedness.
About USV Pvt. Ltd.
USV is a leading pharmaceutical company known for its high-quality generics and active pharmaceutical ingredients (APIs). With a strong presence in both domestic and international markets, USV prides itself on its regulatory compliance and robust manufacturing standards.
Role Overview: QA – QMS (Formulation)
Department: Quality Assurance
Section: QMS (Formulation)
Designation: Assistant Manager / Deputy Manager
Experience: 10–14 Years
Qualification: B Pharm / M.Pharm / MSc
Location: Daman
This leadership QA position involves deep exposure to manufacturing investigations, compliance management, and risk assessment compilation. The selected candidate will play a pivotal role in ensuring regulatory compliance, market complaint handling, and audit readiness within the Formulation QMS section.
Key Responsibilities
H2: Regulatory & QMS Responsibilities
- Execution and timely closure of manufacturing investigations.
- Coordination for handling market complaints and product recalls.
- Preparation and review of Nitrosamine Risk Assessments (NRAs).
- Compilation and documentation of Elemental Impurity Risk Assessments (EIRAs).
- Implementing corrective and preventive actions (CAPAs).
H3: Audit & Compliance
- Ensure audit readiness at all times for regulatory bodies.
- Maintain and update QMS documentation per GMP and ICH guidelines.
- Align with evolving regulatory changes and ensure site-level compliance.
Desired Candidate Profile
- Education: B Pharm, M.Pharm, or MSc in Chemistry/Pharmaceutical Sciences.
- Experience: 10–14 years in QA (Formulation) – must include QMS exposure.
- Preferred Industry: Regulated market exposure (e.g., USFDA, MHRA, TGA).
- Location Preference: Willing to relocate or commute to Daman.
Why Join USV?
- Opportunity to work in a globally recognized pharma company
- Exposure to advanced regulatory compliance frameworks
- Strong learning and growth environment
- Attractive compensation aligned with industry benchmarks
Application Process
Interested and qualified professionals are invited to share their updated resumes at:
recruiterdamanusv@usv.in
Please mention “QA – QMS Application – Daman” in the subject line of your email. Early applicants will be given preference
Summary Table
| Company Name | USV Pvt. Ltd. |
|---|---|
| Current Vacancies | Quality Assurance – QMS (Formulation) |
| Required Education | B Pharm / M.Pharm / MSc |
| Experience Required | 10–14 Years |
| Location | Daman |
To apply for this job email your details to recruiterdamanusv@usv.in
