USV Pharma Hiring Quality Control Officer & Executive
- Company Overview
- Job Role & Responsibilities
- 1. QC – Validation – Officer
- 2. QC – Raw Material (RM) – Sr. Officer / Executive
- 3. QC – GLP – Sr. Executive
- Eligibility / Qualifications
- Location & Salary
- Application Process
- Why Join USV Pharma?
- FAQs
- Summary Table
USV Pharma QC Vacancies – B Pharm/MSc – Daman Plant
Apply for Quality Control Officer & Executive roles at USV Pharma Daman. B Pharm/MSc graduates with 2–12 years experience required. USFDA approved plant
USV Private Limited, a trusted name in the pharmaceutical industry, is expanding its Quality Control (QC) team at the USFDA-approved manufacturing facility in Daman. This is a golden opportunity for skilled pharma professionals to join a reputed organization with a legacy of excellence and innovation in healthcare.
Company Overview
USV Private Limited is a leading pharmaceutical company with a strong global presence, focusing on high-quality formulations and innovative healthcare solutions. With decades of trust in the industry, USV is known for its compliance-driven culture, cutting-edge research, and robust manufacturing capabilities. The Daman site is USFDA approved, reflecting the company’s commitment to international quality standards.
Job Role & Responsibilities
1. QC – Validation – Officer
- Conduct analytical method validation and maintain complete documentation.
- Operate and maintain laboratory instruments as per SOPs.
- Ensure regulatory compliance during QC processes.
2. QC – Raw Material (RM) – Sr. Officer / Executive
- Perform sampling and testing of raw materials as per pharmacopoeial guidelines.
- Maintain detailed records and ensure data integrity.
- Support audits and regulatory inspections with accurate documentation.
3. QC – GLP – Sr. Executive
- Calibrate QC instruments and ensure accuracy.
- Prepare working standards for laboratory testing.
- Ensure compliance with GLP, GMP, and audit requirements.
Eligibility / Qualifications
- Educational Background: B. Pharmacy, MSc (Chemistry, Pharmaceutical Sciences, Microbiology, Biotechnology).
- Experience Requirement:
- QC Validation: 2–4 years.
- QC Raw Material: 4–8 years.
- QC GLP: 8–12 years.
- Key Skills:
- Strong knowledge of GMP, GLP, and QC protocols.
- Hands-on experience with analytical instruments.
- Documentation and compliance expertise.
Location & Salary
- Job Location: Daman, India.
- Salary: Competitive, as per experience and industry benchmarks.
Application Process
Interested candidates can apply by sending their updated CVs to:
Important: Mention the role in the subject line when applying (e.g., Application for QC – Validation – Officer).
Why Join USV Pharma?
- Opportunity to work at a USFDA-approved facility.
- Be part of a reputed pharma company with strong market credibility.
- Career growth in Quality Control with advanced training.
- Competitive pay and employee benefits.
FAQs
1. Who can apply for USV Pharma QC roles?
Candidates with B Pharm or MSc qualifications and 2–12 years of QC experience can apply.
2. What is the location of the job?
The positions are based at USV’s USFDA-approved plant in Daman.
3. How should I apply?
Send your CV to sanafatma.khan@usv.in and mention the department and role in the subject line.
4. What is the salary offered?
USV Pharma offers a competitive salary package in line with qualifications and experience.
5. Are freshers eligible?
No, these positions require 2–12 years of relevant QC experience.
Summary Table
| Category | Details |
|---|---|
| Company | USV Private Limited |
| Vacancies | QC Validation Officer, QC Raw Material Sr. Officer/Executive, QC GLP Sr. Executive |
| Required Education | B. Pharmacy, MSc (Chemistry, Pharmaceutical Sciences, Biotechnology, Microbiology) |
| Experience | 2 to 12 years (role-specific) |
| Location | Daman, India |
| Salary | Best in Industry |
To apply for this job email your details to sanafatma.khan@usv.in