USV Hiring Quality Assurance – QMS (Formulation)

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/M.Sc 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 M.Sc 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 / M.Sc

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 M.Sc 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

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