What a Sr. Quality Engineer contributes to Cardinal Health

• Schedule, execute, and evaluate scientifically and statistically sound qualification experiments complying with all regulatory requirements.

• Assure entire process and required inputs function in a consistent and repeatable manner, and comply with regulatory requirements, product license requirements, and policies affecting final product integrity.

• Coordinates schedules involving manufacturing equipment to maximize equipment utilization.

• Prepares documentation dossiers on completed studies that summarize the experimental results, specifications, and conformance to defined acceptance criteria.

• Provides technical support to various departments as needed.

• Develops policies, programs, SOPs, and Quality standards to meet current industry, corporate Quality, and external Regulatory requirements.

Accountabilities

• Conducts & develops validation and qualification protocols, projects and studies supporting manufacturing facility start-up and operation. Validation documentation to ensure products are manufactured in accordance with cGMP, pharmaceutical regulatory agencies, manufacturer, and Cardinal Health specifications/requirements.

• Maintains close contact with various functions to assure effective communication on challenges and opportunities related to validation.

• Provides technical support as needed.

• Develops policies, programs, SOPs, and Quality standards to meet current industry, corporate Quality, and external Regulatory requirements regarding validation.

• Supports the facility in internal and external regulatory inspections.

• Works directly with management, contract customers, and/or contract engineers.

• Maintain effectiveness of the Quality System components relevant to this position.

• Works autonomously with minimal supervision.

• Develops, maintains, and enforces Cardinal Health compliance standards.

• Learns and carries out laboratory procedures or operate equipment as needed to perform qualification testing.

• Performs other job duties as assigned.

Qualifications

• Bachelors degree in Chemical Engineering, Mechanical Engineering, Chemistry, Metrology or related science field, or equivalent work experience preferred

• 2 or more years of relevant work experience as a Validation Engineer, Quality Assurance Engineering, or Quality Validation Consultant working with 21 CFR 210, 211 in the FDA regulated industry (Pharmaceutical or Medical Device).

• Experience with equipment qualification, software validation, test method validation, and/or process validation.

• Validation and Technology Transfer process and experience with writing procedures/ reports and execution of laboratory test.

• Must be detail oriented, organized, able to multi-task, a self-starter, and self-motivated.

• Must be proficient in Microsoft Word and Microsoft Excel and possess strong technical writing skills.

• Preferred: Experience working with radiopharmaceuticals

Performance Expectations

• Demonstrates a commitment to the organizations mission, vision and values supporting organizational decisions and behaviors. Contributes to the development and implementation of systems and processes ensuring strategic goal attainment.

• Works as part of a team with others and shows respect and values diversity toward others.

• Demonstrates efforts to discovering, meeting and advocating for the customers 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.

• The 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.

What is expected of you and others at this level

• Develops processes and procedures to implement functional strategies.

• Role models Cardinal Healths high ethical standards and code of conduct.

• Builds confidence and respect of others through a positive and energizing style.

• Interprets internal/external business issues and adapts work priorities in own area.

• Strives for operational excellence by continually challenging old methods or ways of thinking and taking responsible risks to maximize results; serves as a role model in innovative thinking and in focusing on quality within work.

• Effectively solicits and explains difficult concepts and persuades others to adopt a point of view; states own point of view.

• Responsible for being a culture champion by participating in the development, monitoring and sustainment of the culture that is an integral part of the Indy manufacturing site philosophy and vision. The incumbent is responsible for embracing and demonstrating the culture of energy, passion and positive atmosphere while delivering superb customer service.

Anticipated salary range:$68,500.00-$97,800.00

Bonus eligible:No

Benefits:Cardinal Health offers a wide variety of benefits and programs to support health and well-being.

• 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

Application window anticipated to close:8/17/2026

*if interested in opportunity, please submit application as soon as possible.