Sr. Production Operator

Orano

Brownsburg, IN(remote)

JOB DETAILS
SKILLS
Asepsis, Biotech and Pharmaceutical, Cancer, Career Development, Change Control, Cleanroom, Continuous Improvement, Detail Oriented, Documentation, Energy & Utilities, Environmental Protection Agency (EPA), Equipment Maintenance/Repair, Federal Laws and Regulations, GMP (Good Manufacturing Practices), High School Diploma, Identify Issues, Lift/Move 50 Pounds, Manufacturing, Manufacturing/Industrial Processes, Nuclear Medicine, Nuclear Power, OSHA, Process Development, Process Engineering, Process Improvement, Production Management, Quality Assurance, Quality Control, Regulations, Regulatory Compliance, Regulatory Requirements, Reporting Skills, Staff Training, Standard Operating Procedures (SOP), State Laws and Regulations, Time Management, Training/Teaching, Waste Disposal
LOCATION
Brownsburg, IN
POSTED
1 day ago


General Information

Name

Sr. Production Operator

Ref #

14409

Posting Date

Tuesday, April 28, 2026

Country

United States

Region

Indiana

City

Brownsburg (IN)

Business Unit (BU)

CORP

Type ofEmployment

Permanent/Regular

Desired Starting Date

25-05-2026

Work Schedule

Full time

Remote Work

In office

Job

N - LABORATORY

Description

Description

Orano Med, a subsidiary of Orano USA, is at the forefront ofresearch 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
  • Quality/continuous improvement:
    • 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
    • Mentor new employees
    • Train new employees
    • 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
  • Cleanroom operations: gowning, cleaning, EM, aseptic technique
  • 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
  • Attention to detail; meticulous execution/documentation
  • Attendance: dependable, on time; flexible for variable schedule
  • Work well under direct supervision or independently
  • Time management
  • Stand for 6+ hours
  • Lift/move 50 lbs repeatedly/routinely
  • Wear cleanroom PPE
Requirements

All candidates must meet the following minimum requirements in order to be considered for this opportunity. Candidates who exceed minimum qualifications may be considered for a higher-level position.

Benefits
  • Competitive compensation
  • Health, Dental, and Vision insurance - with generous employer contributions
  • 401(k) with employer matching and contribution amounts
  • Life insurance and Short- and Long-Term Disability insurance provided by the company
  • Generous Paid Time Off and holiday schedules
  • Numerous Training and Development opportunities
  • and more...


Orano Group

Present in the United States for 60 years, Orano USA is a leading technology and services provider to the U.S. commercial and federal markets.
Orano's activities in the U.S. include developing uranium enrichment facility in Oak Ridge, TN ; packages and transportation of uranium & nuclear fuel assemblies ; fabricating & installing used nuclear fuel dry storage canisters and casks, conducting pool-to-pad used nuclear fuel transfers ; providing solutions to the National Labs and to the Dept of Energy ; and supplying U.S. nuclear energy utilities with uranium, conversion, and enrichment services.
In the nuclear medicine field, Orano Med is at the forefront of research in nuclear medicine and is developing a new generation of targeted therapies against cancer using the unique properties of lead-212.

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 form 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.

About the Company

O

Orano