Officer - QC ( RM)

The Officer – QC (RM) will be responsible for performing analytical testing, documentation, and quality assurance of raw materials, in-process samples, and finished products. The ensures that all materials meet defined specifications and supports validation, calibration, and compliance activities within the Quality Control laboratory.

Roles and Responsibilities:

• Perform inward entry, sampling, and analysis of raw materials, semi-finished products, finished products, process validation samples, rinse water, and cleaning validation samples.
• Ensure all testing is conducted as per approved specifications, standard test procedures, and SOPs.
• Coordinate with external laboratories for outsourced testing, including sample dispatch, tracking, and timely receipt of analytical reports.
• Review and verify external laboratory reports to ensure compliance with quality standards and regulatory requirements.
• Perform calibration of laboratory instruments and equipment as per defined schedules and maintain calibration records.
• Support qualification activities including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) of instruments and equipment.
• Maintain proper management of chemicals, reagents, and reference standards, including inventory control, labeling, and storage conditions.
• Ensure compliance with Good Laboratory Practices (GLP), Good Documentation Practices (GDP), and data integrity (ALCOA+) principles.
• Maintain and update all QC-related documentation, registers, logbooks, and records in an accurate and timely manner.
• Perform disposal of tested samples, chemicals, and waste materials as per SOPs and EHS guidelines.
• Monitor laboratory conditions and ensure proper housekeeping and cleanliness in the QC area.
• entify any out-of-specification (OOS), out-of-trend (OOT), or abnormal results and report them promptly for investigation.
• Participate in root cause analysis (RCA) and support implementation of corrective and preventive actions (CAPA).
• Assist in method validation, method transfer, and verification activities when required.
• Ensure proper labeling, storage, and traceability of all samples and materials within the laboratory.
• Coordinate with QA, Production, and other departments for smooth sample flow and timely analysis.
• Support internal and external audits by maintaining audit-ready documentation and providing required information.
• Ensure adherence to safety protocols and use of personal protective equipment (PPE) during all laboratory activities.
• Track and maintain stability samples and related documentation as per stability protocols.
• Contribute to continuous improvement initiatives to enhance laboratory efficiency and quality systems.
• Ensure timely completion of assigned testing activities to support batch release timelines.
• Maintain confidentiality and integrity of analytical data and laboratory records.

USV Private Limited is an Indian pharmaceutical company dedicated to delivering high-quality medicines and healthcare solutions. With a strong focus on innovation, research, and patient care, the company serves both domestic and global markets.

Our Story

USV began its journey with a vision to provide reliable and effective healthcare solutions. Over the years, the company has grown into a well-established pharmaceutical organization known for its commitment to quality and innovation.

Through continuous investment in research and development, USV has strengthened its capabilities in delivering advanced formulations and improving patient outcomes.

Our Mission

• To provide high-quality and affordable healthcare solutions
• To enhance patient outcomes through innovation and research
• To maintain excellence in pharmaceutical manufacturing
• To build long-term trust with healthcare professionals and patients

Our Vision

To be a trusted global pharmaceutical company recognized for quality, innovation, and patient-centric healthcare solutions.

Our Services / What We Offer

USV Private Limited offers a wide range of pharmaceutical solutions, including:

• Development and manufacturing of pharmaceutical formulations
• Research-driven healthcare products
• Solutions across multiple therapeutic segments
• Global distribution of medicines

Why Choose Us

• Strong focus on research and innovation
• Commitment to quality and compliance
• Trusted presence in domestic and international markets
• Patient-centric approach to healthcare
• Continuous improvement in products and processes

Our Team

USV is supported by a team of experienced professionals, scientists, and healthcare experts who are dedicated to delivering high-quality pharmaceutical solutions and advancing medical science.

Infrastructure / Technology

The company operates advanced manufacturing and research facilities designed to meet global quality standards. Its infrastructure supports innovation, efficiency, and consistent product quality.

Our Commitment

USV Private Limited is committed to improving healthcare by delivering safe, effective, and affordable medicines. The company emphasizes ethical practices, innovation, and quality in all aspects of its operations.