Executive - IPQA

The Executive – IPQA will be responsible for overseeing in-process quality assurance activities on the shop floor, ensuring adherence to SOPs, BMR/BPR requirements, and regulatory standards. The involves line clearance, in-process checks, sampling, documentation review, and validation support to maintain product quality and compliance throughout the manufacturing lifecycle.

Roles and Responsibilities:

• Perform line clearance for dispensing, granulation, blending, compression, capsule filling, coating, and packing activities as per SOPs and batch records.
• Ensure that production areas are free from previous product residues, labels, and materials to avoid mix-ups and cross-contamination.
• Monitor day-to-day activities in areas such as day store, change part room, quarantine area, and accessory room for compliance with procedures.
• Verify logbooks, environmental monitoring records, inward/outward registers, and inventory records for accuracy and completeness.
• Conduct in-process quality checks during compression, capsule filling, coating, and packing operations as per BMR/BPR and SOP requirements.
• Perform sampling at various stages including blending, compression, coating, capsule, and packing as per approved sampling plans.
• Monitor and support process validation activities, including validation batches and sample collection as per protocols.
• Ensure adherence to cGMP, GDP, and data integrity (ALCOA+) principles during all IPQA activities.
• Maintain and update IPQA-related registers such as semi-finished sample register, validation sample register, rinse water register, control sample register, and finished sample register.
• Perform calibration of IPQA instruments and ensure calibration status is current and documented.
• entify and report deviations, non-conformances, and quality issues observed during manufacturing and initiate appropriate actions.
• Participate in investigation of deviations, OOS/OOT results, and support CAPA implementation.
• Ensure proper status labeling of materials, equipment, and areas throughout the manufacturing process.
• Coordinate closely with Production, QA, and QC teams to ensure smooth and compliant operations.
• Review batch records and related documents in real-time to ensure accuracy and compliance with procedures.
• Support internal and external audits by maintaining audit-ready documentation and providing necessary inputs.
• Monitor environmental conditions and ensure compliance with specified limits in manufacturing areas.
• Ensure proper handling, storage, and traceability of samples collected during various stages.
• Assist in implementation of continuous improvement initiatives to enhance product quality and process efficiency.
• Maintain discipline, cleanliness, and good housekeeping practices in all IPQA-controlled areas.
• Ensure completion of required training programs and adherence to updated SOPs and regulatory requirements.
• Support qualification and validation activities related to equipment and processes when required.
• Ensure compliance with safety and EHS guidelines during all quality assurance activities.

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.