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UPS Supply Chain Solutions

QA Associate

UPS Supply Chain Solutions pune, Maharashtra, India

Transportation, Logistics, Supply Chain and Storage · 10,001+ employees

Sep 30
qa Mid (2-5 yrs) Full-time India
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About the role

The QA Associate monitors the distribution center's quality systems to ensure compliance with drug and medical device regulations. They are responsible for conducting facility inspections, managing standard operating procedures, and coordinating corrective and preventative actions.

What they look for

Quality Assurance GMP Standard Operating Procedures Regulatory Compliance Auditing Corrective Actions Preventative Measures Recordkeeping Data Analysis Process Improvement Change Control Clinical Logistics Supply Chain Management Pharmaceutical Regulations Medical Device Regulations

Requirements

The role requires a Bachelor's degree in a science-related field and experience in the pharmaceutical, healthcare, or food industry. A QPIC/AQPIC designation is preferred to support regulatory audit activities.

Full description

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Explore your next opportunity at a Fortune Global 500 organization. Envision innovative possibilities, experience our rewarding culture, and work with talented teams that help you become better every day. We know what it takes to lead UPS into tomorrow—people with a unique combination of skill + passion. If you have the qualities and drive to lead yourself or teams, there are roles ready to cultivate your skills and take you to the next level.

Job Description:

Together, we are Marken, UPS Healthcare Precision Logistics. As the clinical and advanced therapy part of UPS Healthcare, we reach patients faster, with greater scalability and access to new pathways throughout the supply chain. With our One UPS advantage and comprehensive service portfolio, including Polar Speed's in-network pharmacies, we are optimally positioned to keep our clients competitive in an increasingly complex market.

Job Summary

This position monitors the overall Quality System status of the distribution center. This position acts in compliance to drug, medical device, and local regulations. Ensures quality processes are maintained through the implementation of procedures, training, and regular inspections.

Responsibilities

  • Ensures all staff is trained in their respective job functions, including GMP.
  • Writes and revises Standard Operating Procedures as required.
  • Conducts regular inspections of the facility and recordkeeping, including summarization and reporting of findings. Coordinate or assist with corrective actions and preventative measures.
  • Communicates with clients and provides information during external audits
  • Liaises with Health Canada officials during regulatory audits.
  • Provides feedback and assistance to Customer/Client QA related questions and concerns.
  • Monitors the processes and systems within the Department to ensure regulatory compliance and effective operation.
  • Investigates discrepancies and problems, and advise the appropriate individuals of the findings.
  • Assists in development of pro-active strategies as a preemptive measure against potential future problems with systems or processes.
  • Completes NCR reports and change control requests and provide necessary follow-up.
  • Performs maintenance, support, and continuous improvements of Quality Systems.
  • QPIC designation duties.

Qualifications:

  • Pharmaceutical, healthcare or food industry experience - Preferred
  • Quality Assurance experience - Preferred
  • Bachelor’s Degree in Science related field (or internationally comparable degree) required - Preferred
  • QPIC/AQPIC designation - Preferred

Employee Type:  

Permanent UPS is committed to providing a workplace free of discrimination, harassment, and retaliation.

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