USV Pvt Ltd, one of India’s leading pharmaceutical companies, has announced a new recruitment drive for experienced professionals at its Daman manufacturing facility. The company is hiring for Quality Control (QC – OSD) and QC Validation departments. Candidates with experience in USFDA-approved formulation companies are encouraged to apply.

If you have expertise in HPLC, GC, Assay, Dissolution, Method Validation, or ICP-MS, this is an excellent opportunity to join a globally recognized pharmaceutical organization.

Overview

Particular Details

Company Name

USV Pvt Ltd

Job Location

Daman

Industry

Pharmaceutical

Departments

QC (OSD), QC Validation

Positions

Senior Officer, Executive, Sr. Executive

Experience

4–9 Years / 5–8 Years

Qualification

B.Pharm, M.Pharm, M.Sc

Employment Type

Full Time

Preferred Candidates

Immediate Joiners

Selection Mode

Resume Shortlisting & Interview

About USV Pvt Ltd

USV Pvt Ltd is a 63-year-old healthcare company with a strong presence in more than 65 countries. The company is recognized as the No.1 Oral Anti-Diabetics manufacturer and operates a USFDA, MHRA, and EU-approved manufacturing facility at Daman. USV is known for its commitment to quality, innovation, integrity, and employee development.

Available Job Openings

1. QC (OSD) – FG/Stability

Position

Senior Officer

Executive

Experience

5 to 8 Years

Qualification

B.Pharm

M.Pharm

M.Sc

Required Skills

HPLC Analysis

Gas Chromatography (GC)

Assay Testing

Dissolution Testing

Pharmaceutical Analytical Techniques

Stability Sample Analysis

GMP & Documentation

2. QC Validation – Analytical Method Validation

Positions

Senior Officer

Executive

Sr. Executive

Experience

4 to 9 Years

Qualification

B.Pharm

M.Pharm

M.Sc

Required Skills

Analytical Method Validation

Validation Protocol Preparation

Validation Execution

HPLC

ICP-MS

GC

Analytical Documentation

Regulatory Compliance

Eligibility Criteria

Applicants should have:

B.Pharm, M.Pharm or M.Sc qualification.

Relevant pharmaceutical industry experience.

Experience in USFDA-approved formulation companies.

Strong analytical and documentation skills.

Knowledge of cGMP, GLP and regulatory guidelines.

Immediate joining availability is preferred.

Why Join USV Pvt Ltd?

Work with an industry-leading pharmaceutical company.

Career growth opportunities.

Learning and professional development.

Exposure to global regulatory standards.

Strong values, integrity and trust.

Modern USFDA-approved manufacturing facility.

Important Note

Only candidates from USFDA-approved formulation companies are eligible to apply.

Immediate joiners will be given preference.

How to Apply

Eligible candidates should email their updated CV.

Email ID: sanafatma.khan@usv.in

Email Subject Format: Department – Position

Example: QC – Senior Officer

Required Technical Skills

HPLC Operation & Troubleshooting

Gas Chromatography (GC)

Dissolution Testing

Assay Analysis

Method Validation

Stability Testing

ICP-MS

Analytical Documentation

GMP & GLP Compliance

Data Integrity Practices

Selection Process

Resume Screening

Technical Evaluation

HR Interview

Final Selection

Offer & Joining

5 Technical FAQs

1. What HPLC knowledge is expected for these QC positions?

Candidates should be proficient in HPLC operation, system suitability, troubleshooting, calibration, data interpretation, and pharmaceutical sample analysis according to GMP requirements.

2. What is Analytical Method Validation?

Analytical Method Validation is the process of demonstrating that a test method is reliable, accurate, precise, specific, linear, robust, and suitable for its intended purpose as per ICH guidelines.

3. Why is Dissolution Testing important in OSD QC?

Dissolution testing measures the drug release profile from tablets or capsules and ensures consistent product quality, bioavailability, and regulatory compliance.

4. What regulatory guidelines should candidates know?

Candidates should have working knowledge of USFDA, MHRA, EU GMP, ICH Q2(R2), cGMP, GLP, Data Integrity (ALCOA+), and laboratory documentation practices.

5. What is the role of ICP-MS in pharmaceutical laboratories?

ICP-MS (Inductively Coupled Plasma Mass Spectrometry) is used for elemental impurity analysis to ensure pharmaceutical products comply with ICH Q3D and global regulatory standards.

Conclusion

USV Pvt Ltd’s latest recruitment at the Daman plant offers an excellent opportunity for experienced QC (OSD) and QC Validation professionals to build a rewarding career in a globally recognized pharmaceutical company. Candidates meeting the eligibility criteria and possessing experience in USFDA-approved formulation companies should submit their applications at the earliest.