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Nuclear Manufacturing Chemist
2 months ago
Anticipated Salary Range: $66,500 - $95,000
Bonus Eligibility: No
Benefits Overview: Cardinal Health provides a comprehensive array of benefits and programs aimed at enhancing health and well-being.
- Medical, dental, and vision insurance
- Paid time off plan
- Health savings account (HSA)
- 401k retirement savings plan
- Access to wages prior to payday with myFlexPay
- Flexible spending accounts (FSAs)
- Short- and long-term disability insurance
- Work-Life resources
- Paid parental leave
- Healthy lifestyle initiatives
About Cardinal Health:
At Cardinal Health, we are committed to developing innovative products and services that enhance the safety and efficiency of healthcare. Our Nuclear Manufacturing division is dedicated to the production of time-sensitive radiopharmaceuticals within a highly regulated framework (i.e., FDA, NRC, DOT) to assist in patient care through disease diagnosis, staging, and monitoring.
Role of a Nuclear Manufacturing Chemist:
The Nuclear Manufacturing Chemist role is integral to our expanding Technical Operations Manufacturing team within Cardinal Health's Nuclear and Precision Health Solutions division, focusing on the routine production of sponsor radiopharmaceutical products.
This position entails supporting all necessary activities to operate a clinical phase manufacturing facility, ensuring strict compliance with cGMP, environmental health and safety standards, and internal protocols.
Key Responsibilities:
- Assist in manufacturing processes for both internal product development and external sponsors.
- Manage the receipt, sampling, storage, and distribution of all materials required for production.
- Safely handle and transfer radioactive isotopes and final products to end users.
- Oversee daily operations and maintenance of the facility, production equipment, radiation monitoring tools, and testing instruments.
- Execute manufacturing procedures in accordance with standard operating procedures (SOPs), master batch records (MBRs), and established protocols.
- Lead and support investigations and documentation of deviations and non-conformances.
- Maintain cleanliness and functionality of all production equipment, including clean rooms and isolators.
- Document and manage systems related to cGMP compliance, including inventory levels and environmental monitoring.
- Communicate safety, quality, and compliance issues to site leadership.
- Prepare relevant documentation for maintenance activities and update/create SOPs as necessary.
- Provide feedback to the Product Development team regarding client drug manufacturing.
Qualifications:
- Bachelor's degree in life sciences or engineering with a minimum of 2 years of experience in a GMP manufacturing environment within the pharmaceutical or biotechnology sectors.
- Familiarity with the operation, use, and cleaning of laboratory-scale production equipment.
- Ability to work in a controlled environment with a focus on environmental, health, and safety regulations.
- Commitment to data integrity through adherence to standardized procedures and compliance requirements; ability to document work activities promptly.
- Strong motivation to collaborate effectively with others and maintain positive working relationships.
- Willingness to work flexible hours as needed to support production demands.
- Experience in clean rooms/ISO5-8 environments/isolators is advantageous but not mandatory.
- Experience with radioactive isotopes is beneficial but not required.
Cardinal Health values diversity and encourages applications from veterans, individuals with disabilities, and those without a college degree. We are an Equal Opportunity/Affirmative Action employer, ensuring that all qualified applicants 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, or any other status protected by law.