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Senior Specialist, Quality Assurance (Nights) at Cardinal Health in Phoenix, AZ - Apply Now!

Cardinal Health

Senior Specialist, Quality Assurance (Nights) at Cardinal Health in Phoenix, AZ - Apply Now!

full-timePosted: Dec 4, 2025

Job Description

About Cardinal Health

Cardinal Health is a global, integrated healthcare services and products company, connecting the world of healthcare. With over 48,000 employees across North America, Europe, and Asia, we provide pharmaceuticals, medical products, and supply chain solutions that enhance patient outcomes. Our Nuclear & Precision Health Solutions division, including PET Manufacturing Services, specializes in producing PET radiopharmaceuticals critical for disease diagnosis, staging, and monitoring. At our Phoenix, AZ PET facility, we uphold the highest standards of quality and safety in a regulated environment.

Role Overview

The Senior Specialist, Quality Assurance (Nights) plays a pivotal role in our Phoenix PET manufacturing site. This onsite, full-time position (40 hours/week) focuses on nights, typically Monday-Friday 12:00 am-1:30 pm, with every other Saturday 3:30-5:30 am. Flexibility is key, as shifts may adjust based on business needs. You'll ensure products meet stringent CGMP standards under 21 CFR 212, handling documentation, product releases, and collaboration with operations. With a salary range of $67,500-$96,400, this role offers competitive pay in a cleanroom manufacturing pharmacy environment with low radiation exposure under strict regulatory oversight.

Key Responsibilities

In this position, you'll drive quality excellence in PET radiopharmaceutical production:

  • Review CGMP documentation for product release, facilities, equipment, materials, lab controls, packaging, labeling, and production processes.
  • Develop and report key metrics on products and processes as directed by the Regional Quality Manager (RQM).
  • Oversee site compliance with 21 CFR 212 CGMP regulations to guarantee safe, effective products.
  • Manage documentation quality, including control, retention, and archival for all CGMP activities.
  • Partner with operations to embed quality systems and CGMP requirements into daily workflows.
  • Execute product release per CGMP protocols and escalate discrepancies promptly to RQM.

Work Environment Details

Operate in a controlled manufacturing pharmacy: clean, orderly, well-lit, with low-moderate noise. Handle radioactive materials under safe, monitored conditions regulated by state, federal, and internal quality teams. Routine radiation monitoring and training ensure exposures stay within guidelines. Physical demands include lifting 30-45 lbs and multitasking in dynamic conditions.

Qualifications & Requirements

We seek detail-oriented professionals with quality assurance expertise:

  • Bachelor's degree in a related field or equivalent work experience (preferred).
  • 2-4 years of relevant experience (preferred).
  • 1-2 years in Quality Assurance or cGMP-regulated environments (preferred).
  • Strong written and verbal English communication skills.
  • Pharmaceutical, medical device, or ISO experience (plus).
  • Ability to lift 30-45 lbs, manage multiple tasks, and assess operating conditions.

At this level, apply working knowledge to moderate-scope projects, resolve technical issues within parameters, and receive general guidance on new initiatives. Work is reviewed for accuracy and reasoning.

Benefits & Perks

Cardinal Health invests in your well-being with comprehensive benefits:

  • Medical, dental, and vision coverage.
  • Paid time off and parental leave.
  • Health Savings Account (HSA) and Flexible Spending Accounts (FSAs).
  • 401k savings plan.
  • myFlexPay for early wage access.
  • Short- and long-term disability coverage.
  • Work-Life resources and healthy lifestyle programs.

No bonus eligibility, but robust perks support work-life balance in a mission-driven culture.

Career Growth

Advance in Cardinal Health's quality assurance career path. Gain hands-on CGMP experience in PET manufacturing, positioning you for roles like Quality Manager or Regulatory Affairs Specialist. Our training programs, mentorship, and internal mobility foster long-term growth in healthcare compliance and radiopharmaceuticals. Leverage our global network for skill-building in ISO standards, pharma regulations, and leadership.

Why Join Us

Contribute to life-saving diagnostics at a Fortune 500 leader. Enjoy stability in Phoenix's growing healthcare hub, with a flexible night schedule accommodating work-life needs. Our commitment to safety, compliance, and innovation ensures rewarding impact. Application window closes 2/1/2026—apply now to secure your future in quality assurance.

Role FAQs

Q: Is this role remote? A: No, fully onsite in Phoenix, AZ PET facility.

Q: What shift will I work? A: Nights, Mon-Fri ~12am-1:30pm, every other Sat 3:30-5:30am; flexible per business needs.

Q: Do I need prior pharma experience? A: Preferred but not required; 1-2 years QA/cGMP ideal.

Q: What's the physical environment like? A: Cleanroom pharmacy with radiation handling (safe, monitored levels), lifting up to 45 lbs.

Q: When does the application close? A: Anticipated 2/1/2026; apply ASAP.

Locations

  • Phoenix, Arizona, United States of America

Salary

67,500 - 96,400 USD / yearly

Estimated Salary Range

67,500 - 106,040 USD / yearly

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • CGMP Documentation Reviewintermediate
  • Quality System Managementintermediate
  • Product Release Activitiesintermediate
  • Metrics Reportingintermediate
  • Cross-Functional Collaborationintermediate
  • Regulatory Compliance (21 CFR 212)intermediate

Required Qualifications

  • Bachelor's degree in related field or equivalent experience preferred (experience)
  • 2-4 years of experience preferred (experience)
  • 1-2 years in Quality Assurance and/or cGMP environment preferred (experience)
  • Effective written and verbal English communication (experience)
  • Pharmaceutical or medical device experience a plus (experience)
  • Ability to lift 30-45 lbs and multitask (experience)

Responsibilities

  • Handle CGMP documentation review for product release, facilities, equipment, and production controls
  • Establish and report metrics on products and processes
  • Ensure site compliance with 21 CFR 212 CGMP requirements
  • Manage quality documentation control, retention, and archival
  • Collaborate with operations to drive quality system and CGMP
  • Perform product release activities and escalate issues to Regional Quality Manager

Benefits

  • general: Medical, dental and vision coverage
  • general: Paid time off plan
  • general: Health savings account (HSA)
  • general: 401k savings plan
  • general: Access to wages before pay day with myFlexPay
  • general: Flexible spending accounts (FSAs)
  • general: Short- and long-term disability coverage
  • general: Work-Life resources
  • general: Paid parental leave
  • general: Healthy lifestyle programs

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Cardinal Health logo

Senior Specialist, Quality Assurance (Nights) at Cardinal Health in Phoenix, AZ - Apply Now!

Cardinal Health

Senior Specialist, Quality Assurance (Nights) at Cardinal Health in Phoenix, AZ - Apply Now!

full-timePosted: Dec 4, 2025

Job Description

About Cardinal Health

Cardinal Health is a global, integrated healthcare services and products company, connecting the world of healthcare. With over 48,000 employees across North America, Europe, and Asia, we provide pharmaceuticals, medical products, and supply chain solutions that enhance patient outcomes. Our Nuclear & Precision Health Solutions division, including PET Manufacturing Services, specializes in producing PET radiopharmaceuticals critical for disease diagnosis, staging, and monitoring. At our Phoenix, AZ PET facility, we uphold the highest standards of quality and safety in a regulated environment.

Role Overview

The Senior Specialist, Quality Assurance (Nights) plays a pivotal role in our Phoenix PET manufacturing site. This onsite, full-time position (40 hours/week) focuses on nights, typically Monday-Friday 12:00 am-1:30 pm, with every other Saturday 3:30-5:30 am. Flexibility is key, as shifts may adjust based on business needs. You'll ensure products meet stringent CGMP standards under 21 CFR 212, handling documentation, product releases, and collaboration with operations. With a salary range of $67,500-$96,400, this role offers competitive pay in a cleanroom manufacturing pharmacy environment with low radiation exposure under strict regulatory oversight.

Key Responsibilities

In this position, you'll drive quality excellence in PET radiopharmaceutical production:

  • Review CGMP documentation for product release, facilities, equipment, materials, lab controls, packaging, labeling, and production processes.
  • Develop and report key metrics on products and processes as directed by the Regional Quality Manager (RQM).
  • Oversee site compliance with 21 CFR 212 CGMP regulations to guarantee safe, effective products.
  • Manage documentation quality, including control, retention, and archival for all CGMP activities.
  • Partner with operations to embed quality systems and CGMP requirements into daily workflows.
  • Execute product release per CGMP protocols and escalate discrepancies promptly to RQM.

Work Environment Details

Operate in a controlled manufacturing pharmacy: clean, orderly, well-lit, with low-moderate noise. Handle radioactive materials under safe, monitored conditions regulated by state, federal, and internal quality teams. Routine radiation monitoring and training ensure exposures stay within guidelines. Physical demands include lifting 30-45 lbs and multitasking in dynamic conditions.

Qualifications & Requirements

We seek detail-oriented professionals with quality assurance expertise:

  • Bachelor's degree in a related field or equivalent work experience (preferred).
  • 2-4 years of relevant experience (preferred).
  • 1-2 years in Quality Assurance or cGMP-regulated environments (preferred).
  • Strong written and verbal English communication skills.
  • Pharmaceutical, medical device, or ISO experience (plus).
  • Ability to lift 30-45 lbs, manage multiple tasks, and assess operating conditions.

At this level, apply working knowledge to moderate-scope projects, resolve technical issues within parameters, and receive general guidance on new initiatives. Work is reviewed for accuracy and reasoning.

Benefits & Perks

Cardinal Health invests in your well-being with comprehensive benefits:

  • Medical, dental, and vision coverage.
  • Paid time off and parental leave.
  • Health Savings Account (HSA) and Flexible Spending Accounts (FSAs).
  • 401k savings plan.
  • myFlexPay for early wage access.
  • Short- and long-term disability coverage.
  • Work-Life resources and healthy lifestyle programs.

No bonus eligibility, but robust perks support work-life balance in a mission-driven culture.

Career Growth

Advance in Cardinal Health's quality assurance career path. Gain hands-on CGMP experience in PET manufacturing, positioning you for roles like Quality Manager or Regulatory Affairs Specialist. Our training programs, mentorship, and internal mobility foster long-term growth in healthcare compliance and radiopharmaceuticals. Leverage our global network for skill-building in ISO standards, pharma regulations, and leadership.

Why Join Us

Contribute to life-saving diagnostics at a Fortune 500 leader. Enjoy stability in Phoenix's growing healthcare hub, with a flexible night schedule accommodating work-life needs. Our commitment to safety, compliance, and innovation ensures rewarding impact. Application window closes 2/1/2026—apply now to secure your future in quality assurance.

Role FAQs

Q: Is this role remote? A: No, fully onsite in Phoenix, AZ PET facility.

Q: What shift will I work? A: Nights, Mon-Fri ~12am-1:30pm, every other Sat 3:30-5:30am; flexible per business needs.

Q: Do I need prior pharma experience? A: Preferred but not required; 1-2 years QA/cGMP ideal.

Q: What's the physical environment like? A: Cleanroom pharmacy with radiation handling (safe, monitored levels), lifting up to 45 lbs.

Q: When does the application close? A: Anticipated 2/1/2026; apply ASAP.

Locations

  • Phoenix, Arizona, United States of America

Salary

67,500 - 96,400 USD / yearly

Estimated Salary Range

67,500 - 106,040 USD / yearly

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • CGMP Documentation Reviewintermediate
  • Quality System Managementintermediate
  • Product Release Activitiesintermediate
  • Metrics Reportingintermediate
  • Cross-Functional Collaborationintermediate
  • Regulatory Compliance (21 CFR 212)intermediate

Required Qualifications

  • Bachelor's degree in related field or equivalent experience preferred (experience)
  • 2-4 years of experience preferred (experience)
  • 1-2 years in Quality Assurance and/or cGMP environment preferred (experience)
  • Effective written and verbal English communication (experience)
  • Pharmaceutical or medical device experience a plus (experience)
  • Ability to lift 30-45 lbs and multitask (experience)

Responsibilities

  • Handle CGMP documentation review for product release, facilities, equipment, and production controls
  • Establish and report metrics on products and processes
  • Ensure site compliance with 21 CFR 212 CGMP requirements
  • Manage quality documentation control, retention, and archival
  • Collaborate with operations to drive quality system and CGMP
  • Perform product release activities and escalate issues to Regional Quality Manager

Benefits

  • general: Medical, dental and vision coverage
  • general: Paid time off plan
  • general: Health savings account (HSA)
  • general: 401k savings plan
  • general: Access to wages before pay day with myFlexPay
  • general: Flexible spending accounts (FSAs)
  • general: Short- and long-term disability coverage
  • general: Work-Life resources
  • general: Paid parental leave
  • general: Healthy lifestyle programs

Target Your Resume for "Senior Specialist, Quality Assurance (Nights) at Cardinal Health in Phoenix, AZ - Apply Now!" , Cardinal Health

Get personalized recommendations to optimize your resume specifically for Senior Specialist, Quality Assurance (Nights) at Cardinal Health in Phoenix, AZ - Apply Now!. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Senior Specialist, Quality Assurance (Nights) at Cardinal Health in Phoenix, AZ - Apply Now!" , Cardinal Health

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score

Tags & Categories

Cardinal Health CareersQuality Assurance JobsCGMP CompliancePET RadiopharmaceuticalsHealthcare ManufacturingCareers in Phoenix AZCardinal Health CareersQuality Assurance JobsCGMP CompliancePET RadiopharmaceuticalsHealthcare ManufacturingCareers in Phoenix AZ

Answer 10 quick questions to check your fit for Senior Specialist, Quality Assurance (Nights) at Cardinal Health in Phoenix, AZ - Apply Now! @ Cardinal Health.

Quiz Challenge
10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.