Senior Nuclear Manufacturing Technician – 2nd Shift

Cardinal Health, Inc.

Indianapolis (IN)

On-site

USD 62,000 - 84,000

Full time

8 days ago
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Benefits offered by this job

Medical/dental/vision
PTO
HSA
401k
Flex pay
FSAs
Disability insurance
Work-Life resources
Parental leave
Wellness programs

Job summary

Cardinal Health, Inc. is hiring for a Nuclear Manufacturing position in Indianapolis on the 2nd shift (3:00 pm – 11:30 pm). The role is full-time, 40 hours weekly, with training on 1st shift.

Responsibilities include executing cGMP SOPs, inventory management, quality monitoring, and collaboration with cross-functional teams to meet production goals. Qualifications include 2–4 years of experience, a High School diploma or equivalent, and experience with bulk formulation or filling.

Qualifications

  • Adheres to SOPs under cGMP requirements.
  • Maintains inventory accuracy and traceability.
  • Monitors product quality according to SOPs.
  • Maintains and cleans equipment and facilities.
  • Collaborates with cross-functional teams to meet production goals.
  • Follows detailed processing instructions and adapts to improvements.

Responsibilities

  • Execute SOPs in a cGMP environment, ensuring GDP practices.
  • Manage inventory levels and materials.
  • Monitor and verify quality per SOPs and records.
  • Perform routine maintenance and cleaning of equipment.
  • Collaborate with cross-functional teams to meet production demands.
  • Adhere to large set of SOPs and adapt to process improvements.
  • Learn and use technology to support manufacturing processes.
  • Be knowledgeable in Formulation and Filling.

Skills

SOP adherence
cGMP knowledge
Inventory management
Quality monitoring
Teamwork
Attention to detail

Education

High School diploma, GED or equivalent

Job description

Cardinal Health, Inc. is hiring for a Nuclear Manufacturing position in Indianapolis on the 2nd shift (3:00 pm – 11:30 pm). The role is full-time, 40 hours weekly, with training on 1st shift.

Responsibilities include executing cGMP SOPs, inventory management, quality monitoring, and collaboration with cross-functional teams to meet production goals. Qualifications include 2–4 years of experience, a High School diploma or equivalent, and experience with bulk formulation or filling.

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