Cardinal Health · 7 hours ago
Quality Line Inspector
Indianapolis, IN
Full-time
Onsite
Entry Level
$68K/yr - $96K/yr
2+ years expCardinal Health is a leading healthcare services and products company. They are seeking a Quality Line Inspector responsible for maintaining quality records, performing real-time QA reviews, and ensuring compliance with GMP and regulatory standards.
Health CareHospitalMedical
Responsibilities
Maintains accurate and current Quality records
Performs real-time QA review of batch documentation and other GMP related documents
Issuance and reconciliation of product labels for production
Perform AQL testing for visual inspection
Understands technical/release product issues and evaluate their potential impact on product quality and compliance
Champion Quality, GMP compliance and EHS/Radiation Safety practices
Ability to network across business and functional units to achieve positive outcomes
Assists Quality Management with FDA and other regulatory agency activities
Demonstrates efforts to discovering, meeting and advocating for the customer’s needs
Takes actions to continually improve quality and safety in daily work. Actively participates in improving work processes to meet and exceed expectations. Identifies opportunities for improvement based on process observations, outcome measures, and feedback
Reports errors in a timely and appropriate manner. Takes initiative and is accountable for areas of responsibility meeting regulatory requirements including but not limited to maintaining required trainings as appropriate to position requirements
Demonstrated ability to act calmly and patiently when working under pressure and/conditions of stress. Maintains integrity, composure, communicates with honesty, transparency, clarity and promotes alternative perspectives
Performs other job duties as assigned
Qualification
Required
Demonstrates knowledge of quality systems and approaches
Demonstrates an understanding of the relevant regulations, standards and operating procedures
Demonstrates ability to perform investigations / root cause analysis and develop corrective actions
Demonstrates an understanding of the requirements and has the ability to perform gap assessments to those requirements
Demonstrates an understanding of quality concepts such as: cost of quality, analytical metrics and / or statistics, trending, quality planning, validation, CAPA and problem solving
Works cross-functionally and has the ability to interpret the requirements as well as educate and influence others on those requirements
Maintains accurate and current Quality records
Performs real-time QA review of batch documentation and other GMP related documents
Issuance and reconciliation of product labels for production
Perform AQL testing for visual inspection
Understands technical/release product issues and evaluate their potential impact on product quality and compliance
Champion Quality, GMP compliance and EHS/Radiation Safety practices
Ability to network across business and functional units to achieve positive outcomes
Assists Quality Management with FDA and other regulatory agency activities
Demonstrates efforts to discovering, meeting and advocating for the customer's needs
Takes actions to continually improve quality and safety in daily work. Actively participates in improving work processes to meet and exceed expectations. Identifies opportunities for improvement based on process observations, outcome measures, and feedback
Reports errors in a timely and appropriate manner. Takes initiative and is accountable for areas of responsibility meeting regulatory requirements including but not limited to maintaining required trainings as appropriate to position requirements
Demonstrated ability to act calmly and patiently when working under pressure and/conditions of stress. Maintains integrity, composure, communicates with honesty, transparency, clarity and promotes alternative perspectives
Performs other job duties as assigned
Preferred
Bachelor's in science related field (processing engineering, Chemistry, Biology) or equivalent work experience
2+ years' experience in related field
2 years of relevant work experience working with 21 CFR 210, 211 in the FDA regulated industry (Pharmaceutical or Medical Device)
Possess an understanding of cGMP/compliance requirements for cosmetic and pharmaceutical products
Working knowledge of Microsoft Office Suite specifically Microsoft Word and Excel
Working knowledge of Adobe editing software
Working knowledge of Document Management software (Trackwise and/or Smartsolve)
Demonstrated ability to manage timelines and priorities
Demonstrated to work independently with minimum guidance
Demonstrated to multi-task and focus attention to detail
Benefits
Medical, dental and vision coverage
Paid time off plan
Health savings account (HSA)
401k savings plan
Access to wages before pay day with myFlexPay
Flexible spending accounts (FSAs)
Short- and long-term disability coverage
Work-Life resources
Paid parental leave
Healthy lifestyle programs
Company
Cardinal Health
Cardinal Health is a manufacturer and distributor of medical and laboratory products.
10001+ employees
H1B Sponsorship
Cardinal Health has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (128)
2024 (116)
2023 (140)
2022 (158)
2021 (106)
2020 (142)
Funding
Current Stage
Public CompanyTotal Funding
$1.08B2025-08-28Post Ipo Debt· $1B
2006-08-16Post Ipo Debt· $78M
1983-08-12IPO
Leadership Team
Aaron Alt
Chief Financial Officer
T
Tony Caprio
Executive Vice President
Recent News
Morningstar.com
2026-01-16
Company data provided by crunchbase