Supervisor, QC (Chemistry) Method Transfer

What a Supervisor, 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.

• Reports to Manager, Quality Control (Chemistry).
• Demonstrates detail-oriented attention in all facets of responsibilities.
• Performs analytical evaluation and/or testing of products or processes.
• Has knowledge of testing methods, product usage, and applicable regulations and standards.
• Established test methodology and adheres to established policies and procedures.
• Provides technical guidance and training to others on SOPs and quality guidelines.

Accountabilities

• Exhibits Cardinal Health's high ethical standards and code of conduct.
• Applies expertise to improve effectiveness and solves standard and non-standard problems, providing guidance to employees.
• Sets priorities for technology transfer team to ensure task completion, coordinates work activities with other shifts/teams (1st/2nd/Weekend).
• Assists team in the achievement of goals/commitments, achieving own goals/commitments regardless of obstacles.
• Has in-depth knowledge of work processes and tools within own area and can function as a subject matter expert (SME).
• Partners with leadership to make decisions, often difficult and/or unpopular, that impact the work of subordinates within job family; influences subordinates to support decision by presenting rationale/business case.
• Role models Cardinal Health's high ethical standards and code of conduct.
• Recognizes development needs and capability gaps in own area and arranges specific projects/assignments to address needs.
• Provides direction in discussing and creating development plans.
• Aligns individual goals for self and others with work area/functional goals.
• Works within budgetary/ financial objectives set by manager, applying knowledge of profit drivers to work processes within own area.
• Builds confidence and respect of others through a positive and energizing style.
• Is aware of internal/external business issues and adapts work priorities in own area.
• Works with customers to anticipate and interpret customer needs and business challenges by identifying quality and service-oriented customer solutions and shares key learnings with others.
• Encourages subordinates to strive 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.
• Actively builds relationships across functions/businesses that bring value to the company, encouraging the participation and perspectives of all team members, regardless of background; mentors and empowers others to achieve success
• Effectively listens to and explains difficult issues to reach shared understanding and build alignment
• 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. Is responsible for embracing and demonstrating the culture of energy, passion and positive atmosphere while delivering superb customer service.

Responsibilities

• Coordinates and supervises the daily activities of Chemists or business support staff in the performance of technology transfer, method validation/verification and method optimization

• Serves as the liaison between Cardinal Health Quality Control and Client Quality Control in the performance of technology transfer, method validation/verification/development/optimization

• Is a quality lead for the QC Chemistry team

• Identifies quality events and works with QA/QC management to ensure each event is handled in accordance with site procedures and regulatory requirements

• Oversees chemists and contractors who operate analytical equipment, perform analytical tests, interpret results and documents findings in accordance with SOPs and regulatory requirements.

• Trains, assesses and coaches team in laboratory procedures, techniques and career development as needed.

• Performs technical review of investigations, deviations and CAPAs.

• Oversees and authors written procedures and other documents, including amendments.

• Ensures results are consistent with acceptable test parameters and reports abnormal findings from Analytical tests to the Manager of Quality Control (Chemistry).

• Ensures employees operate within guidelines, all necessary testing is carried out, and the associated records provided to the QA department in a timely manner to ensure project timelines are met

• Assists in the recommendation for approval or rejection of testing methods and modes of analysis

• Develops and applies practices which will enable the laboratory to meet and exceed desired customer and regulatory standards in a cost-effective fashion.

• Assists in and/or conduct all laboratory investigations of discrepancies to resolve problems and works with other members of management to ensure corrective action or preventative actions are implemented in a timely manner.

• Remains aware of developments in chemistry by reading current technical literature and attending technical meetings.

• Makes recommendations to other members of management to improve the performance of the laboratories.

• Ensures proper laboratory hygiene and monitors the storage conditions for materials and products used in the labs.

• Executes or participates in internal/external laboratory quality audits, as directed by management to ensure that all associated records are evaluated.

• Assists in training efforts and development of laboratory personnel.

• Works closely with operations regarding the interpretation and implementation of any elements that the system of the Quality Management System, to resolve differences and ultimately ensure the system is understood and applied uniformly.

• Ensures all work is carried out in a manner demonstrating support for and adherence to the Company's Safety Policy and Procedures, Quality Policy and Procedures, Ethics Policy, Environmental management System, Vision and Strategy, and to exercise good judgement, common sense, and diplomacy in doing so.

• Produces and reviews personal development plans for team members, identifying and providing appropriate training.

• Ensures any Safey, Quality, or Site actions are completed effectively and in a timely manner and that the escalation process exists to raise quality issued to the appropriate levels of management.

• Performs other job duties as assigned.

Qualifications

• Bachelor's degree in chemistry or related science field. Experience in radiochemistry, nuclear pharmacy, or health physics preferred.
• 5+ years of relevant work experience with 21 CFR 210, 211 in the FDA regulated industry (Pharmaceutical or Medical Device).
• Must have experience with equipment qualification, software validation, test method validation, and/or process validation.
• Has experience in authoring a variety of documentation such as SOPs, Change Controls, CAPAs, Deviations (Nonconformance), and Laboratory Investigations.
• Must understand the validation and technology transfer process and have experience with writing procedures/reports and execution of laboratory tests.
• Must be 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.

Anticipated salary range: $82,100.00-$117,200.00

Bonus eligible: Yes

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: 1/9/2027 *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.

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 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.

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