Senior Specialist, Quality Control Chemist II (2nd Shift)

Cardinal Health; Indianapolis (IN); On-site; USD 67,000 - 93,000; Full time

Job summary

A leading healthcare company is seeking a Senior Specialist, Quality Control Chemist II for the 2nd shift. This role involves performing analytical evaluations and ensuring compliance with quality standards. The ideal candidate will have a Bachelor’s degree and relevant experience in the FDA regulated industry. Join a team dedicated to improving healthcare products and services.

Benefits

Medical, dental and vision coverage

Paid time off plan

Health savings account (HSA)

401k savings plan

Flexible spending accounts (FSA)

Short- and long-term disability coverage

Work-Life resources

Paid parental leave

Healthy lifestyle programs

Qualifications

• 2+ years of experience in FDA regulated industry preferred.
• Experience in authoring documentation like SOPs and Change Controls.

Responsibilities

• Performs analysis of incoming materials and product samples.
• Executes method verification and validation protocols.
• Authors and optimizes SOPs and testing forms.

Skills

Analytical Evaluation

Technical Writing

Communication

Education

Bachelor’s Degree in Science

Tools

Microsoft Word

Microsoft Excel

Job description

Senior Specialist, Quality Control Chemist II (2nd Shift)

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Senior Specialist, Quality Control Chemist II (2nd Shift)

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At Cardinal Health, we’re developing the innovative products and services that make healthcare safer and more productive. Join a growing, global company genuinely committed to making a difference for our customers and communities.

What a Senior Specialist, Quality Control (Chemistry) contributes to Cardinal Health

Quality Control is responsible for the analysis and inspection of products or processes for compliance with specifications and standards.

• Performs visual assessment and analytical evaluation or testing of products/processes.
• Demonstrates knowledge of testing methods, product usage, and applicable regulations and standards.
• Adheres to established policies and procedures.
• Establishes test methodology and may contribute to the development of policies and procedures.
• May provide technical guidance and training to others on SOPs and quality guidelines.
  
  

What is expected of you and others at this level

• Exhibits Cardinal Health's high ethical standards and code of conduct.
• Approaches work situations with a positive and energizing style.
• Possesses in-depth knowledge of work processes and tools within own area and can function as a Subject Matter Expert (SME) for processes, tools, and equipment.
• Gain awareness of other departments at site. Seek to understand the functions of those departments and the points of interaction between QC and your role.
• Exhibit professional conduct, respect for others, and understands how to be successful in a team environment.
• Is detail oriented, organized, has the ability to multi-task, and is self-motivated. Is aware of internal/external business issues and adapts work priorities in own area.
• Demonstrates strong communication skills. Effectively listens to and explains difficult issues to reach shared understanding and build alignment.
• 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.
• Has 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.
• Actively builds relationships across functions/businesses that bring value to the company, encouraging the participation and perspectives of all team member, regardless of background.
• Identifies quality events and aids in any associated investigations.
  
  

Responsibilities

• Performs analysis of incoming materials, in-process, and product samples.
• Executes method verification, validation, and/or transfer protocols, analytical equipment qualification protocols, or computer system validation test scripts, as needed.
• Performs stability testing in alignment with stability protocols at the prescribed cadence.
• Performs laboratory investigations, change controls, deviations, and corrective/preventative actions as needed.
• Authors and optimizes SOPs, analytical testing forms, and other documents as necessary.
• Performs special projects or tasks as necessary based on skill set and/or development goals and business needs.
• Champion Quality, cGMP compliance, and EHS/Radiation Safety practices.
• Performs other job duties as assigned.
  
  

Qualifications

• Bachelor’s degree or previous work experience in a similar role or related science field preferred.
• 2+ years of relevant work experience working with 21 CFR 210, 211 in the FDA regulated industry (Pharmaceutical or Medical Device) preferred.
• Has experience in authoring a variety of forms of documentation such as SOPs, Change Controls, CAPAs, Deviations and Laboratory Investigations preferred
• Proficient in Microsoft Word and Microsoft Excel and possess strong technical writing skills.
  
  

Physical/ Mental Requirements

• The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.
• While performing the duties of this job, the employee is regularly required to talk or hear. The employee is frequently required to stand; walk; use hands to finger, handle or feel; and reach with hands and arms; balance; stoop, kneel, crouch or crawl. The employee must occasionally lift or move up to 25 pounds. Specific vision abilities required by the job include close vision, distance vision, color vision, peripheral vision, depth perception and the ability to adjust focus.
  
  

Work Environment

• The primary work environment consists of a professional office environment within a radiopharmaceutical manufacturing facility, the materials warehouse as well as the laboratory setting.
• The facility is operated under well-controlled and closely monitored conditions that are regulated by both State and Federal agencies, and that are enforced by the corporate internal quality and regulatory groups. Each staff member will receive specific training in keeping radiation exposures within regulatory guidelines and he/she will be routinely monitored for their exposure to radiation. Noise levels are considered low to moderate.
  
  

Schedule

• 2nd Shift - Anticipated 3:00 pm - 12:00 am
• Potential to work 1st shift, to cover PTO of other analysts
• Initial training for this role will be provided on 1st shift.
  
  

Anticipated salary range: $67,500- $92,400

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: 7/7/2025 *if interested in opportunity, please submit application as soon as possible.

The salary range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate’s geographical location, relevant education, experience and skills and an evaluation of internal pay equity.

Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply.

Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law.

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Quality Assurance

• Industries

  Hospitals and Health Care, Transportation, Logistics, Supply Chain and Storage, and Medical Equipment Manufacturing

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