USV Private Limited – Hiring for Quality Assurance & Quality Control Positions at USFDA Formulation Manufacturing Plant – Apply Now

USV is inviting applications from experienced pharmaceutical quality professionals for senior-level opportunities at its USFDA formulation manufacturing plant in Daman, near Vapi, Gujarat. The current openings are available in Quality Assurance and Quality Control functions for candidates with extensive experience in QA, IPQA, audit compliance, investigations and QC review activities.

Professionals looking to build their careers in a USFDA-compliant manufacturing environment can review the position-wise eligibility and submit their updated CV.

Open Positions at USV

AGM – Quality Assurance

Department: Quality Assurance
Section: QA (OSD) – General QA / Audit Compliance / Investigations
Position: AGM
Experience Required: 18 to 24 Years

The position is suitable for senior pharmaceutical professionals with extensive experience in Oral Solid Dosage quality systems, general quality assurance activities, regulatory audit compliance and investigation management.

Candidates should have strong knowledge of pharmaceutical quality systems and regulated manufacturing environments.

Manager – Quality Assurance

Department: Quality Assurance
Section: IPQA – Oral Solids
Position: Manager
Experience Required: 15 to 18 Years

Candidates should have relevant experience in In-Process Quality Assurance activities for Oral Solid Dosage manufacturing operations.

Professionals with practical knowledge of shop-floor quality systems, manufacturing compliance, documentation and quality monitoring can submit their CV for this position.

Manager – Quality Control

Department: Quality Control
Section: QC Reviewer – Oral Solids & Sterile
Position: Manager
Experience Required: 15 to 18 Years

This position requires experienced Quality Control professionals with relevant exposure to QC review activities in Oral Solid and Sterile pharmaceutical manufacturing.

Candidates should possess strong analytical documentation and quality review experience in a regulated pharmaceutical environment.

Job Location

Daman, Near Vapi, Gujarat

The selected candidates will work at USV’s USFDA formulation manufacturing plant.

Experience Required

USV is currently hiring senior and experienced pharmaceutical professionals with 15 to 24 years of relevant industry experience.

Experience requirements vary according to the position:

AGM – QA: 18 to 24 Years
Manager – IPQA: 15 to 18 Years
Manager – QC Reviewer: 15 to 18 Years

Key Areas of Experience

Candidates with relevant experience in the following pharmaceutical quality functions may be considered:

• General Quality Assurance
• OSD Quality Assurance
• Audit Compliance
• Investigations
• In-Process Quality Assurance
• Oral Solid Dosage Manufacturing
• QC Review
• Oral Solids
• Sterile Manufacturing
• Pharmaceutical Quality Systems
• USFDA-Regulated Manufacturing Environment

Why Join USV?

The hiring opportunity offers experienced professionals the chance to work in a USFDA-compliant formulation manufacturing environment.

The company highlights opportunities for professional growth, continuous learning and working with an experienced pharmaceutical team focused on quality.

How to Submit Your CV

Interested and eligible candidates can send their updated CV to:

Email: rohan.kale@usv.in

Candidates should ensure that their resume clearly mentions their current designation, total experience, relevant department and experience in QA, IPQA or Quality Control.

Important Note

Applicants should carefully review the experience requirements before submitting their CV. These positions are intended for senior pharmaceutical professionals with relevant experience in regulated formulation manufacturing operations.

Candidates are advised to use only the official email address mentioned in the recruitment notification for submitting their resume.

Frequently Asked Questions (FAQ)

Q1. Which company is hiring for QA and QC positions?

USV is hiring experienced professionals for Quality Assurance and Quality Control positions at its formulation manufacturing plant.

Q2. Which positions are currently available?

The current openings are for AGM – Quality Assurance, Manager – Quality Assurance and Manager – Quality Control.

Q3. What experience is required for USV jobs?

Candidates should have 15 to 24 years of relevant pharmaceutical industry experience, depending on the position.

Q4. Which departments have vacancies?

Openings are available in the Quality Assurance and Quality Control departments.

Q5. What are the key areas of experience required?

Relevant experience is required in General QA, Audit Compliance, Investigations, IPQA, Oral Solids, Sterile Manufacturing and QC Review activities.

Q6. Where is the USV job location?

The job location is Daman, near Vapi, Gujarat.

Q7. How can candidates submit their CV?

Eligible candidates can send their updated CV to rohan.kale@usv.in.

Q8. Is experience in a regulated pharmaceutical environment important?

Yes. These senior-level roles are focused on quality functions at a USFDA formulation manufacturing plant, so relevant regulated pharmaceutical manufacturing experience is important.