Nuclear Manufacturing Technician I
Job Details
Hiring Department
MRR Products & Svcs Mfg
A life-saving operation in the middle of America — the University of Missouri Research Reactor (MURR) — needs you to help guide its future. MURR is expanding its critical cancer-fighting and medical isotope production.
MURR’s reactor is the highest-power university research reactor in the United States, operating at 10 megawatts, 6.5 days a week and 52 weeks a year. The MURR facility enables research across many disciplines – From investigating ancient cultures and how plants respond to their environment, to analyzing industrial materials and developing radiopharmaceuticals that have lifesaving clinical applications. The MURR facility is a reliable resource for researchers, scientists, engineers and students across the country.
Be a part of the future of fighting cancer and saving lives.
Be a part of MURR
Job Description
MURR is seeking a Nuclear Manufacturing Technician to join the Research Reactor production team. The successful candidate will have a strong attention to detail, enjoy teamwork, and have a commitment to excellence working within a cGMP environment.
Key Duties Performed by This Position Will Include
This position participates and assists in the cross-functional manufacturing of cutting-edge and life-saving medical radioisotopes generated at MURR. These are used in the diagnostics and treatments of patients around the globe. Employees in this team work in a cleanroom and lab focused FDA GMP and NRC regulated environment alongside health physics, microbiology, quality control, engineering, and quality assurance to complete time-sensitive production-focused processes. Skills, expertise, and responsibility will increase over time with this position due to extensive on the job training. Some of the entry level responsibilities are below:
- Assisting with the routine production of solutions. This entails preparing the laboratory and documentation for each process with a focus on regulatory compliance.
- Production apparatus setup and cleaning, calibration, preparation of reagents and documentation requisite to planned processing evolutions.
- Maintaining FDA Good Manufacturing Processes within an NRC (Nuclear Regulatory Commission) regulated facility.
- Reading and following standard operating procedures (SOPs) in support of production and dispensing of the product.
- Will contribute to the authoring, revision, and approval of GMP documentation including SOPs, change controls, and deviations.
- Assist in various project and process development as needed.
- This position may also assist with the management of key inventories and consumables associated with routine production.
- Contribute to continuous improvement and process enhancement and development projects and initiatives to improve reliability and consistency.
- Work in this position is comprised of a wide variety of standardized tasks, from disinfection of clean rooms, to handling hazardous materials, analytically preparing solutions with narrow specifications, and manipulating equipment remotely inside of a Hot Cell.
Successful candidates will be persuasive communicators with exceptional organizational and time management skills. They must demonstrate the following durable skills: leadership, character, collaboration, communication, creativity, critical thinking, mindfulness, growth mindset, and fortitude. Additionally, customer service, confidentiality, integrity, and a commitment to university values in their activities.
Must be available for reliable and consistent onsite work.
Shift
Monday - Friday 8:00 a.m. - 5:00 p.m. during training period. Once training is complete, the position will require shift work including work during holidays and inclement weather. The schedule of work will be discussed during interviews.
Minimum Qualifications
High school diploma or equivalent combination of education and experience and at least 1 years of experience from which comparable knowledge and skills can be acquired is necessary.
Preferred Qualifications
- Preference will be given to those with cGMP/GLP experience, general laboratory experience, and hazardous/radioactive materials handling experience
- Experience with aseptic Technique, cleanroom, manipulator operation, writing, and root cause analysis.
- Associates or Bachelor’s Degree in a STEM field preferred.
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