Job Description
QC Executive Finished Goods – Quality Control | USV Pvt Ltd | Daman, Gujarat, India
USV Pvt Ltd is hiring experienced professionals for the role of QC Executive Finished Goods at its pharmaceutical manufacturing operations in Daman, Gujarat, India. This full-time opportunity is suitable for candidates with 8 to 10 years of experience in pharmaceutical quality control, finished goods analysis, laboratory operations, quality documentation, analytical testing, GMP compliance, batch release coordination, quality assurance support, inspection systems, and regulated pharmaceutical quality environments.
The selected candidate will manage finished goods quality control activities, perform analytical and physical testing of pharmaceutical products, maintain laboratory documentation and quality records, coordinate with production and quality assurance departments, support batch release activities, monitor laboratory workflow schedules, ensure adherence to GMP and quality procedures, participate in quality review meetings, support inspection readiness activities, and maintain discipline within pharmaceutical laboratory systems. Candidates should possess strong knowledge of pharmaceutical quality operations and analytical laboratory procedures.
This role provides valuable exposure to pharmaceutical quality systems, finished goods inspection workflows, analytical laboratory operations, compliance management activities, and quality assurance coordination within a reputed pharmaceutical organization. Professionals interested in pharmaceutical quality management and laboratory operations can build strong technical and operational expertise through this opportunity.
Location
Daman, Gujarat, India
Employment Type
Full-time
Experience Required
8 to 10
About USV Pvt Ltd
USV Pvt Ltd operates in the pharmaceutical industry specializing in healthcare manufacturing, quality-focused pharmaceutical operations, regulated production systems, and advanced pharmaceutical quality management activities.
Key Responsibilities
Manage finished goods quality control activities.
Perform analytical and physical testing operations.
Maintain laboratory documentation and quality records.
Coordinate with production and QA departments.
Support batch release and quality verification activities.
Monitor laboratory workflow schedules and timelines.
Ensure adherence to GMP and quality procedures.
Participate in quality reviews and inspection preparation.
Maintain discipline within laboratory systems.
Assist in achieving pharmaceutical quality objectives.
Required Skills
Strong understanding of pharmaceutical quality control systems.
Knowledge of finished goods analytical testing.
Awareness of GMP and regulated laboratory workflows.
Communication and coordination management abilities.
Problem-solving and analytical thinking expertise.
Documentation and reporting management skills.
Time management and workflow planning capabilities.
Attention to quality accuracy and compliance standards.
Team coordination and multitasking abilities.
Adaptability to regulated pharmaceutical environments.
Educational Qualification
MSc
Industry
Pharmaceutical
Why Join USV Pvt Ltd?
USV Pvt Ltd offers professionals opportunities to work in advanced pharmaceutical quality systems with exposure to regulated manufacturing and analytical laboratory operations.
How to Apply
Interested candidates can apply through ACKJOBS and complete the application process for this pharmaceutical quality control opportunity.
Check our website — www.ackjobs.com — regularly for the latest updates in the job market. Join our WhatsApp and social media groups from the website.
USV Pvt Ltd is hiring experienced professionals for the role of QC Executive Finished Goods at its pharmaceutical manufacturing operations in Daman, Gujarat, India. This full-time opportunity is suitable for candidates with 8 to 10 years of experience in pharmaceutical quality control, finished goods analysis, laboratory operations, quality documentation, analytical testing, GMP compliance, batch release coordination, quality assurance support, inspection systems, and regulated pharmaceutical quality environments.
The selected candidate will manage finished goods quality control activities, perform analytical and physical testing of pharmaceutical products, maintain laboratory documentation and quality records, coordinate with production and quality assurance departments, support batch release activities, monitor laboratory workflow schedules, ensure adherence to GMP and quality procedures, participate in quality review meetings, support inspection readiness activities, and maintain discipline within pharmaceutical laboratory systems. Candidates should possess strong knowledge of pharmaceutical quality operations and analytical laboratory procedures.
This role provides valuable exposure to pharmaceutical quality systems, finished goods inspection workflows, analytical laboratory operations, compliance management activities, and quality assurance coordination within a reputed pharmaceutical organization. Professionals interested in pharmaceutical quality management and laboratory operations can build strong technical and operational expertise through this opportunity.
Location
Daman, Gujarat, India
Employment Type
Full-time
Experience Required
8 to 10
About USV Pvt Ltd
USV Pvt Ltd operates in the pharmaceutical industry specializing in healthcare manufacturing, quality-focused pharmaceutical operations, regulated production systems, and advanced pharmaceutical quality management activities.
Key Responsibilities
Manage finished goods quality control activities.
Perform analytical and physical testing operations.
Maintain laboratory documentation and quality records.
Coordinate with production and QA departments.
Support batch release and quality verification activities.
Monitor laboratory workflow schedules and timelines.
Ensure adherence to GMP and quality procedures.
Participate in quality reviews and inspection preparation.
Maintain discipline within laboratory systems.
Assist in achieving pharmaceutical quality objectives.
Required Skills
Strong understanding of pharmaceutical quality control systems.
Knowledge of finished goods analytical testing.
Awareness of GMP and regulated laboratory workflows.
Communication and coordination management abilities.
Problem-solving and analytical thinking expertise.
Documentation and reporting management skills.
Time management and workflow planning capabilities.
Attention to quality accuracy and compliance standards.
Team coordination and multitasking abilities.
Adaptability to regulated pharmaceutical environments.
Educational Qualification
MSc
Industry
Pharmaceutical
Why Join USV Pvt Ltd?
USV Pvt Ltd offers professionals opportunities to work in advanced pharmaceutical quality systems with exposure to regulated manufacturing and analytical laboratory operations.
How to Apply
Interested candidates can apply through ACKJOBS and complete the application process for this pharmaceutical quality control opportunity.
Check our website — www.ackjobs.com — regularly for the latest updates in the job market. Join our WhatsApp and social media groups from the website.