USV Walk-In Production, QA, QC and Engineering
USV Hiring QA QC Production Jobs | Daman Pharma
USV Private Limited hiring for Production, QA, QC and Engineering roles in Daman. B.Pharm, M.Pharm, M.Sc, ITI and Diploma candidates can apply.
Pharmaceutical professionals looking for USV jobs in Daman, sterile injectable manufacturing jobs, quality assurance vacancies, quality control careers, and engineering jobs in pharmaceutical companies have an excellent opportunity to advance their careers with USV Private Limited. The company has announced a walk-in interview drive in Ahmedabad for multiple openings at its USFDA, MHRA, and EU-approved manufacturing facility located in Daman.
USV is recruiting experienced professionals across Production (Sterile Injectables), Quality Assurance, Quality Control, Microbiology, Technology Transfer, Plant Maintenance, Utilities, and Engineering departments. Opportunities are available for Junior Operators, Operators, Senior Operators, Technicians, Officers, Senior Officers, Executives, and Senior Executives.
Candidates possessing qualifications such as B.Pharm, M.Pharm, M.Sc, ITI, Diploma, B.Sc, B.E., and B.Tech can apply based on the role requirements. Professionals with exposure to regulated pharmaceutical manufacturing environments and global regulatory standards are especially encouraged to attend.
Company Overview
USV Private Limited is one of India’s most respected pharmaceutical and healthcare organizations with over 63 years of industry excellence. The company has built a strong global presence spanning more than 65 countries and is recognized for delivering high-quality pharmaceutical products across multiple therapeutic segments.
Its manufacturing facilities operate according to stringent international quality standards and are approved by major regulatory agencies including the USFDA, MHRA, and European authorities. These approvals reflect the company’s commitment to pharmaceutical quality, compliance, patient safety, and continuous innovation.
Working at USV provides professionals with opportunities to gain exposure to advanced sterile manufacturing operations, regulatory inspections, technology transfer projects, pharmaceutical quality systems, and global healthcare manufacturing standards.
Job Role & Responsibilities
Production – Sterile Injectables
Positions Available
- Junior Operator
- Operator
- Senior Operator
- Senior Officer
- Executive
Sections
- Aseptic Filling
- Vial Washing
- Sterile Manufacturing
Experience Required
- 2 to 10 Years
- 5 to 8 Years (for Officer and Executive positions)
Professionals in production operations will be responsible for:
- Operating sterile manufacturing equipment
- Managing aseptic filling processes
- Monitoring vial washing activities
- Maintaining batch manufacturing records
- Following cGMP requirements
- Ensuring compliance with sterile manufacturing procedures
- Supporting production targets while maintaining product quality
- Participating in deviation investigations and corrective actions
Candidates with experience in regulated sterile injectable facilities will be preferred.
Technology Transfer
Position
- Executive
- Senior Executive
Experience
- 5 to 8 Years
Technology Transfer professionals will be responsible for:
- Product transfer activities
- Process scale-up coordination
- Manufacturing process optimization
- Technology transfer documentation
- Cross-functional collaboration
- Process validation support
- Regulatory compliance activities
This role is suitable for professionals experienced in pharmaceutical manufacturing technology and product lifecycle management.
Plant Maintenance
Position
- Junior Technician
- Technician
Qualification
- ITI
- Diploma
- B.Sc
Experience
- 2 to 8 Years
Responsibilities include:
- Preventive maintenance activities
- Equipment troubleshooting
- Utility system maintenance
- Documentation management
- Equipment reliability improvement
- Breakdown maintenance support
Engineering – OSD
Position
- Senior Officer
- Executive
Qualification
- B.E.
- B.Tech (Electrical)
Experience
- 5 to 8 Years
Engineering professionals will handle:
- Equipment maintenance planning
- Electrical system monitoring
- Utility management
- Compliance documentation
- Validation support
- Engineering projects
- Equipment qualification activities
Utility Department
Candidates with experience in pharmaceutical utilities, electrical systems, HVAC operations, water systems, and maintenance functions will be valuable additions to the engineering team.
Quality Department Opportunities
Quality Control (OSD)
Section
- Finished Goods (FG)
- Stability Studies
- Raw Material Analysis
Position
- Senior Officer
- Executive
Qualification
- B.Pharm
- M.Pharm
- M.Sc
Experience
- 5 to 8 Years
Key responsibilities include:
- Raw material testing
- Finished product analysis
- Stability study execution
- Laboratory documentation
- Regulatory compliance
- Data integrity management
- Instrument operation and maintenance
- Analytical investigation support
Sterile Quality Assurance (IPQA)
Position
- Officer
- Senior Officer
Qualification
- B.Pharm
- M.Pharm
- M.Sc
Experience
- 3 to 8 Years
Responsibilities include:
- In-process quality assurance activities
- Batch record review
- GMP compliance monitoring
- Deviation handling
- Documentation review
- Process verification
- Audit readiness support
Quality Control – Microbiology
Section
- Sterility Testing
- Environmental Monitoring
Position
- Senior Officer
- Executive
Qualification
- M.Sc Microbiology
Experience
- 4 to 8 Years
Professionals will be responsible for:
- Sterility testing
- Environmental monitoring
- Microbial analysis
- Laboratory investigations
- Data review
- Microbiology documentation
- Compliance with microbiological quality standards
Eligibility / Qualifications
USV is inviting applications from candidates with the following educational backgrounds:
- B.Pharm
- M.Pharm
- M.Sc
- M.Sc Microbiology
- B.Sc
- ITI
- Diploma
- B.E Electrical
- B.Tech Electrical
Preferred Industry Experience
Candidates should possess experience in:
- Sterile Injectable Manufacturing
- Aseptic Operations
- Vial Washing Systems
- Technology Transfer
- Quality Assurance
- Quality Control
- Microbiology
- Pharmaceutical Engineering
- Utility Operations
- Regulatory Compliance
- GMP Documentation
- MHRA Compliance
- USFDA-Regulated Manufacturing
Candidate Prerequisites
USV has specified the following requirements:
- Exposure to USFDA and MHRA audits
- Minimum two years of stability in the current organization
- Relevant pharmaceutical industry experience as per role requirements
Immediate joiners will be given preference during the selection process.
Location & Salary
Job Location: Daman
Walk-In Location: Ahmedabad
Estimated Salary Range
- Junior Operator / Operator: ₹2.8 – ₹5.5 LPA
- Senior Operator: ₹4.5 – ₹7.0 LPA
- Technician: ₹3.5 – ₹6.5 LPA
- Officer / Senior Officer: ₹5.5 – ₹10 LPA
- Executive / Senior Executive: ₹8 – ₹16 LPA
Actual compensation will depend on experience, technical expertise, current salary structure, and interview performance.
Application Process
Walk-In Interview Details
Date: 28 June 2026 (Sunday)
Time: 9:00 AM to 3:00 PM
Walk-In Venue
The Fern Residency
Subhash Bridge Corner, RTO Circle
Keshav Nagar
Ahmedabad, Gujarat – 380027
Documents Required
Candidates should carry:
- Updated CV/Resume
- Aadhaar Card
- Passport Size Photograph
- Latest Salary Slips
- Current CTC Breakup
- Educational Certificates
- Experience Documents
Selection Preference
- Candidates with regulated market exposure
- Professionals having experience in sterile manufacturing
- Immediate joiners
USV encourages eligible professionals to attend the walk-in drive and explore opportunities within one of India’s most trusted pharmaceutical organizations.
Frequently Asked Questions
Who can apply for USV’s walk-in interview?
Candidates with qualifications such as B.Pharm, M.Pharm, M.Sc, M.Sc Microbiology, B.Sc, ITI, Diploma, B.E., and B.Tech can apply based on role-specific requirements.
Where is the job location?
Selected candidates will work at USV Private Limited’s manufacturing facility in Daman.
Is sterile injectable experience mandatory?
For Production, Sterile QA, and related departments, prior experience in sterile injectable manufacturing is highly preferred.
What regulatory exposure is preferred?
Candidates with experience handling USFDA and MHRA audits will have an advantage.
Are freshers eligible?
The current openings primarily require experienced professionals ranging from 2 to 12 years of pharmaceutical industry experience.
What documents should candidates bring?
Applicants should carry their updated resume, Aadhaar card, passport photograph, salary slips, CTC breakup, and educational certificates.
Summary
| Category | Details |
|---|---|
| Company | USV Private Limited |
| Department Vacancies | Production (Sterile Injectables), Technology Transfer, Plant Maintenance, Engineering, Utility, Sterile QA, QC, Microbiology |
| Qualification | B.Pharm, M.Pharm, M.Sc, M.Sc Microbiology, B.Sc, ITI, Diploma, B.E., B.Tech |
| Experience | 2 to 12 Years |
| Location | Daman |
