USV Pharmaceutical Limited Walk-in 26th April 2025 for Officer – Senior Officer – Quality Control

USV Pharmaceutical Limited Walk-in Interview 2025.USV Pharmaceutical Limited Notification full details below.Interested and eligible candidates can attend Interview on scheduled time and venue.

Vacancy details:

• Department: Officer – Senior Officer – Quality Control
• Experience: 02 to 5  years
• Qualification:MS/M.Sc(Science) in Chemistry
• Salary:₹Not Disclosed

Important Details :

• Selection Process: The selection will be on the basis of Interview.
• Mode of Interview: Face to face
• Interview Rounds of Interview: HR

Job Description: Greeting from USV Pharmaceutical Limited !!!

Walk in Interview for Officer / Sr. Officer – Quality Control USV – Vadodara

Location: USV Pvt. Ltd., Savli – Manjusar, Vadodara, Gujarat

Interview Date: 26th April 2025

Time: 10:00 AM to 1:00 PM

Venue: Plot 538 to 540 & 597 to 625, Savli GIDC Road, Manjusar, Alindra, Gujarat 391775

About USV:

Join a legacy of over 62 years of excellence in the pharmaceutical industry! USA, is a trusted global leader in healthcare. Our world-class formulations facility at Savli Manjusar is where innovation meets opportunity.

We are looking for professionals who are presently employed in a pharmaceutical company, with a minimum of two years of continuous experience in their current company.

We respectfully request that only candidates who meet these specific criteria attend the interview.

Experience Range : 2 to 5 Years

Job Summary:

The Raw Material Analyst will be responsible for performing thorough analysis and testing of raw materials used in Oral Solid Dosage (OSD) pharmaceutical manufacturing. This includes physical, chemical, and identification testing to ensure compliance with pharmacopoeial standards (USP, BP, EP, IP) and internal specifications. The analyst will maintain GMP compliance and support continuous improvement in quality standards.

Key Responsibilities:

Perform physical analysis of raw materials including:

Appearance, color, odor

Particle size distribution

Bulk/tapped density

Loss on drying / moisture content

Conduct chemical and quality analysis such as:

Identification tests (e.g., FTIR, UV, TLC)

Assay and content uniformity

pH and solubility tests

Limit tests for impurities, heavy metals, etc.

Ensure raw materials comply with pharmacopoeial standards (USP, BP, EP, IP) and internal SOPs.

Prepare, review, and maintain analytical documentation including worksheets, raw data, and reports.

Operate and calibrate analytical instruments (e.g., UV-Vis, FTIR, HPLC, GC, KF titrator, etc.).

Coordinate with the warehouse and production teams for sampling and material release activities.

Participate in investigations for OOS (Out of Specification), OOT (Out of Trend), and deviations.

Support method verification, validation, and equipment qualification as per regulatory requirements.

Ensure all activities comply with cGMP, GLP, and safety guidelines.

Assist in audits (internal, external, regulatory) by providing relevant documentation.

Candidates are requested to carry copy of their resume