Chemist Consultant, Nuclear Manufacturing (2nd Shift)

Cardinal Health, Inc.; Indianapolis (IN); On-site; USD 79,000 - 114,000; Full time

Job summary

An established industry player is seeking a dedicated professional for their Nuclear Manufacturing division. This role involves ensuring the integrity and compliance of radiopharmaceutical production in a highly regulated environment. You will evaluate and create testing procedures, lead investigations, and maintain manufacturing equipment while adhering to strict safety and quality standards. The company offers a supportive work environment with a commitment to employee well-being and development. If you are passionate about making a difference in patient care and thrive in a collaborative setting, this opportunity is for you.

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

Qualifications

• Bachelor's degree required with 4+ years in GMP manufacturing.
• Experience in clean room environments and safety regulations.

Responsibilities

• Evaluate and adapt testing procedures for radiopharmaceuticals.
• Lead investigations and document production deviations.
• Maintain and repair manufacturing equipment.

Skills

GMP manufacturing experience

Clean room environment experience

Data integrity maintenance

Collaboration and teamwork

Technical problem-solving

Education

Bachelor’s degree in life sciences or engineering

Job description

What Nuclear Manufacturing contributes to Cardinal Health

Manufacturing is responsible for cost of production and maintenance activities including process improvement, supply chain management, quality assurance, employee safety and engagement, and environmental commitment.

Nuclear Manufacturing is responsible for the manufacturing of time sensitive radiopharmaceuticals in an integrity driven, highly regulated environment (i.e. FDA, NRC, DOT) to support patient treatment through disease diagnosis, staging, and monitoring.

Shift/Schedule

• 2nd shift
• Monday - Friday
• 3:00pm - 11:30pm

Responsibilities

• Evaluate, create, adapt, and transfer testing procedures established by internal product development teams and external product sponsors for our Indianapolis theranostics cGMP radiopharmaceutical manufacturing facilities.
• Assist on creation of protocols and controlled documentation necessary to enable the technology transfer and qualification of contracted products. Generate study reports where required.
• Execute equipment qualifications developed in partnership with Validations personnel, as well as provide feedback and improvements to qualifications.
• Lead investigations and document deviations that occurred during routine production activities.
• Facilitate day-to-day operation, maintenance and repair of manufacturing equipment. Clean and maintain all manufacturing equipment.
• Communicate all issues related to safety, quality, and compliance to leadership.
• Perform relevant documentation for maintenance activities, as well as modify and create SOPs.

Qualifications

• Bachelor’s degree in life sciences or engineering with at least four years of experience working in a GMP manufacturing environment in the pharmaceutical or biotechnology industry. A background in product research and development is preferred.
• Experience in working in a clean room environment, paying special attention to environmental, health, and safety regulation. Position may require lifting or moving equipment weighing up to 75 lbs.
• Experience in working directly on client projects and products and providing guidance and support for implementation challenges.
• Commitment to maintain data integrity through strict adherence to standardized procedures and relevant compliance requirements, including the ability to clearly document all work activities in a timely manner.
• Motivation to work effectively and cooperatively with others, and to establish and maintain good working relationships.
• Desire to create, develop, and mature testing processes, and facility and systems infrastructure, to streamline operational efficiency across a broad range of products.
• Flexibility to work periodic off-shift hours to accommodate routine production schedules among qualified facilities.
• Experience working with radioactive isotopes not required but is preferred.

What is expected of you and others at this level

• Applies comprehensive knowledge and a thorough understanding of concepts, principles, and technical capabilities to perform varied tasks and projects.
• May contribute to the development of policies and procedures.
• Works on complex projects of large scope.
• Develops technical solutions to a wide range of difficult problems.
• Solutions are innovative and consistent with organization objectives.
• Completes work; independently receives general guidance on new projects.
• Work reviewed for purpose of meeting objectives.
• May act as a mentor to less experienced colleagues.

Anticipated salary range:$79,700 - $113,800

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:04/22/2025 *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.