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QA System Validation Supervisor
full-timeIndia

Summary

Location

India

Type

full-time

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About this role

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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:

Job Summary

The Healthcare Quality Assurance (QA) System Validation Supervisor provides guidance to UPS Supply Chain Solutions (SCS) Information Technology (IT) department to maintain validation of warehouse and/or support systems utilized for healthcare applications. This position assesses systems being evaluated for use in healthcare applications and provides training and subject matter expertise to achieve and maintain validated status. He/She identifies systems requiring validation, elevates validation issues appropriately, and provides validation expertise. This position manages validation documents, determines applicable regulations, and reviews and approves testing of changes to validated systems.

Job Description

  • Knowledgeable in 21 CFR Part 11, Annex 11, and GAMP 5

  • Updates validation procedures, including change control, training, and audits, to ensure the maintenance of system validation.

  • Writes and reviews technical validation documents (e.g., validation plan, URS, FRS, Risk Assessment, Traceability Matrix, IQ/OQ/PQ/OPQ protocol, report, etc.)

  • Assists in system validation project activities (e.g., writing protocols, reviewing/approving test scripts, drafting validation reports, etc.)

  • Review and approve Change Control requests and assesses the impact on system validation status.

  • Review and approve procedures, forms, and manuals.

  • Perform audit trail reviews and document results.

  • Perform system validation status evaluations and complete reports.

  • Assist with supplier qualification assessment data gathering.

  • Investigate, review, approve, and perform corrective actions for deviations (i.e., nonconformances and CAPAs) and audit findings.

  • Maintains the document management system for healthcare facilities and distribution centers to ensure required documents and data are available for regulatory agency audits and inspections

  • Supports internal and external audits

  • Supports validation project status reports to communicate project goals, contingency plans, and issue resolutions to project teams and clients

  • Supervise direct reports, as appropriate

  • Lead cross functional groups

  • Flexible to work in different time zones

Mandatory Skills: Proficient with Microsoft Office applications (Word, Excel, and PowerPoint)

Qualifications:

  • Bachelor’s degree in a relevant field (e.g., Information Technology, Computer Science, Data Science, or related discipline).

  • Overall, 7 years of experience with 2+ years of experience in quality assurance, manufacturing, or compliance within a GMP-regulated industry.

  • Knowledgeable in 21 CFR Part 11, Annex 11, and GAMP 5

  • Must be an effective collaborator and communicator

  • Must be well organized

  • Must have proficiency with Microsoft Excel, word and PowerPoint.

  • Knowledge of Process Analysis/Continuous Improvement are required

Tasks identified:

  • Provides guidance to UPS Supply Chain Solutions (SCS) Information Technology (IT) and Engineering departments to maintain validation of warehouse and/or support systems utilized for healthcare applications.

  • Identify systems used in healthcare that require validation and assess and evaluate the applications for system validation requirements.

  • Consults with internal groups (e.g., Operations, Business Development, IT, etc.) and investigates and resolves healthcare issues to ensure compliance with rules and regulations.


Employee Type:
 

Permanent


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

Other facts

Tech stack
Quality Assurance,System Validation,Regulatory Compliance,Documentation Management,Change Control,Technical Writing,Collaboration,Communication,Process Analysis,Continuous Improvement,Microsoft Office,Training,Auditing,Risk Assessment,Healthcare Applications,Supplier Qualification

About UPS

Operating in more than 200 countries and territories, we’re committed to moving our world forward by delivering what matters. Beginning as a small messenger service, UPS was started by two enterprising teenagers and a $100 loan. Now, we’re almost 500,000 UPSers strong, with operations around the globe.

As a transportation and logistics leader, we are proud to offer innovative solutions to our customers—both big and small. We also support the communities we serve. Just take a look at The UPS Foundation’s social impact report!

Headquartered in Atlanta, we can be found on the web at ups.com and about.ups.com. Job seekers can visit upsjobs.com to learn more. Our active social media channels include Facebook, Instagram, Twitter, YouTube, and TikTok.

Facebook: www.facebook.com/ups
Instagram: www.instagram.com/ups/
Twitter: www.twitter.com/ups
TikTok: UPS
YouTube: www.youtube.com/ups

Website
https://about.ups.com/
The UPS Foundation’s social impact report:
https://about.ups.com/us/en/social-impact/reporting/the-ups-foundations-social-impact-report.html
Career Site
upsjobs.com

Team size: 10,001+ employees
LinkedIn: Visit
Industry: Truck Transportation
Founding Year: 1907

What you'll do

  • The QA System Validation Supervisor provides guidance to maintain validation of healthcare applications and systems. This role includes managing validation documents, assessing systems for compliance, and supervising direct reports.

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Frequently Asked Questions

What does a QA System Validation Supervisor do at UPS?

As a QA System Validation Supervisor at UPS, you will: the QA System Validation Supervisor provides guidance to maintain validation of healthcare applications and systems. This role includes managing validation documents, assessing systems for compliance, and supervising direct reports..

Why join UPS as a QA System Validation Supervisor?

UPS is a leading Truck Transportation company.

Is the QA System Validation Supervisor position at UPS remote?

The QA System Validation Supervisor position at UPS is based in India, India. Contact the company through Clera for specific work arrangement details.

How do I apply for the QA System Validation Supervisor position at UPS?

You can apply for the QA System Validation Supervisor position at UPS directly through Clera. Click the "Apply Now" button above to start your application. Clera's AI-powered platform will help match your profile with this opportunity and guide you through the application process. You can also learn more about UPS on their website.