Job description
Orano Med is seeking a Facilities Maintenance Engineer for radiopharmaceutical manufacturing at ATLab Indianapolis ("ATLab IND"), a new facility for commercial-scale manufacturing of sterile therapeutic radiopharmaceuticals. The Facilities Maintenance Engineer will oversee the maintenance, optimization, and compliance of our state-of-the-art manufacturing facility. The ideal candidate will ensure that all facility systems operate efficiently, safely, and in alignment with regulatory standards pertinent to the pharmaceutical industry. Facility Maintenance & Optimization:
- Manage and perform preventive, corrective, and predictive maintenance on facility equipment and systems to ensure optimal performance.
- Assess and optimize facility layout and operational systems to enhance efficiency and safety.
Regulatory Compliance:
- Ensure all facility operations comply with FDA cGMP regulations and other relevant standards.
- Develop and maintain Standard Operating Procedures (SOPs) related to facility operations.
Project Management:
- Support projects related to facility modifications, equipment installations, and system upgrades.
Safety & Environmental Stewardship:
- Implement and uphold safety protocols to maintain a secure working environment.
- Manage waste disposal and recycling systems in compliance with environmental regulations.
Documentation & Reporting:
Other responsibilities as needed. Our Full-Time 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
Ideal qualifications
Qualifications Required Education
- Bachelor's degree in Mechanical, Electrical, Industrial Engineering, or a related technical field or equivalent experience.
- Minimum of 3 years of experience in facilities maintenance within an FDA cGMP-regulated environment, preferably in the pharmaceutical or medical device industry.
- Strong knowledge of FDA, ICH, EU, and UK regulations as they apply to manufacturing facilities.
Personality
- Character: radical integrity; honesty; obeys rules/policies/regulations/laws
- Work effectively on simultaneous tasks in a high-pressure environment with tight deadlines
- Detail-oriented; organizational skills; time management; meticulous execution and documentation
Work Environment
- Work in office
- On-Site in Brownsburg, IN
Culture/Personality
- Team-minded; ability to work with cross-functional teams
- Communication: Concise, organized oral/written communication; excellent listening
- Able to thrive and work collaboratively in a fast-paced team environment
- Successful in various situations: independent tasks, following instructions, leading a team
- Seizes opportunities to learn, accept a project, or help with a task
- Overcomes problems by pushing through challenges, seeking resources, asking for help
- Owns the process, makes strong decisions
Orano is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, national origin, age, disability, citizenship, veteran status, marital status, sexual orientation, gender identity, genetic predisposition or carrier status or any other characteristic protected by law.
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Orano Med, LLC.
life insurance, vision insurance, paid time off, 401(k)
May 22, 2025