Production Operator II

Orano; Brownsburg (IN); On-site; USD 45,000 - 60,000; Full time

Benefits offered by this job

Competitive health and wellness programs

401(k) contributions

Industry-leading paid time off

Job summary

Orano is seeking a Production Operator II in Brownsburg, Indiana. The role focuses on routine production and maintaining high standards in a new facility within the nuclear medicine sector. Qualified candidates should have a background in GMP production, a minimum of 2 years of relevant experience, and the ability to work both collaboratively and independently in fast-paced environments. Key benefits include competitive health programs and 401(k) contributions.

Qualifications

• 2+ years of hands-on GMP production experience.
• Experience in quality or production-related roles within a GMP environment.
• Dependable with flexible attendance for variable schedules.

Responsibilities

• Produce routine production while adhering to EHS regulations.
• Collaborate with the Production Supervisor for process improvements.
• Maintain compliance with SOPs and regulatory requirements.

Skills

GMP production of sterile pharmaceuticals

Following detailed SOPs

Quality Management Systems (QMS)

Effective documentation

Ability to work in a fast-paced environment

Education

Associate’s degree or equivalent

High School Diploma and relevant experience

Job description

Orano Med, a subsidiary of Orano USA, is at the forefront of research in nuclear medicine and is developing new therapies against cancer. Based on its unique expertise in the extraction and purification of lead-212 (Pb-212) and radiolabeling technologies, Orano Med is developing innovative Pb-212-based treatments which consist of selectively destroying cancer cells while limiting the impact on surrounding healthy cells.

The top priority for the Production Operator II will be routine production. This position presents the opportunity to help establish a new facility that will meet high standards for quantity, speed, and reliability. A competitive candidate will be energetic and motivated.

Key Responsibilities

• Work with Production Supervisor and Management team to improve the process
• Collaborate with the shift supervisor to ensure the shift is running efficiently while leading by example
• Collaborate with the shift supervisor to train other members of the team
• Writing and reviewing relevant SOPs Help ensure the site is in an audit ready state
• Perform routine cleaning/disinfection of the cleanroom suites
• Complete: reading SOPs, gowning qualification, media fills, process training, bioburden runs, PV runs, tech transf
• Top priority:
  • Daily routine production Follow EHS regulations/guidelines: NRC (ALARA), OSHA, EPA, chemical, waste disposal, state/local regulations, etc.
  • Manufacturing activities following SOPs, using proper aseptic technique
  • Setup production; line clearance; clean/VPHP
  • Troubleshoot urgent problems
  • Identify, document, communicate failures/near misses
• Adhere to SOPs, company policies, regulatory requirements, laws
• Work closely with QC/QA to deliver quality products
• Assist with deviations, OOT/OOS, CAPAs, change controls, audits, inspections
• Collaborate with MS&T and process engineers to identify process improvements and help execute development work needed to implement change
• Cross-train and perform:
  • Cleanrooms: cleaning, EM, restocking
  • Routine radiation surveys, wipe tests
• Other:
  • Maintain paper/electronic batch records, equipment logs, other records
  • Equipment: maintain, qualify, calibrate, prepare, report problems, troubleshooting
  • Maintain stock of materials/supplies; obtain documentation for raw material release
  • Other tasks as needed

Orano strives to provide a total compensation package that brings value to our employees. We also offer highly competitive health and wellness programs, 401(k) contributions, and industry leading paid time off.

In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification from upon hire.

This position requires a pre-employment background check and drug screening.

Orano is an Equal Opportunity Employer. Orano and all subsidiaries abide by applicable legal requirements. We ensure that all personnel actions such as recruitment, compensation, career development, benefits, and company-sponsored training are administered without regard to race, color, religion, sex, national origin, age, disability, sexual orientation, protected veteran, or other protected status.

Qualifications

Education

• Associate’s degree or equivalent (60 college credit hours) with 2+ years of relevant experience, or
• High School Diploma (or equivalent) with 3 or more years of experience in a quality or production-related role within a GMP environment.

Experience

• Hands‑on GMP production of sterile pharmaceuticals 2+ yrs
• Follow detailed SOPs, complete detailed documentation (e.g., batch records)
• QMS in a regulated environment: QA, GDP, SOPs, document control, change control
• Owns the manufacturing process; work well in a fast‑paced, high‑pressure environment with tight deadlines
• Attendance: dependable, on time; flexible for variable schedule
• Work well under direct supervision or independently