The Radiation Control Technician supports the Institute in the area of radiological protection ensuring compliance with state and federal regulations by measuring, assessing and documenting radiological conditions in the workplace. In addition, the incumbent is expected to support other environmental, safety and health disciplines.
Requires an Associates Degree in health physics or radiological science and 3 years experience as a radiological control technician or an equivalent combination of education, training and/or experience from which comparable knowledge, skills and abilities have been attained. Equivalence will be evaluated against ANSI/ANS 3.1-1987 technician qualification criteria.
Candidate must have comprehensive knowledge of the principles of radiation physics and implementation of radiological controls. Must have a demonstrated understanding of applicable OSHA, EPA, NRC, and DOT related regulations. Must be mechanically inclined, able to troubleshoot and make decisions with limited supervision.
Requires strong written and verbal communication skills, the ability to work independently and as a part of a team, as well as a solid understanding of the need to balance customer satisfaction with procedure compliance.
Requires professional-level computer skills to include experience with Microsoft Office and the ability to learn department-specific computer systems as needed.
A post-offer, pre-placement physical examination, ability to obtain required vaccinations, and successful completion of various background checks are required. Applicants must be willing to work in an ABSL-3 environment and with radiation. Ability to gain and maintain access to Kirtland Air Force base (KAFB) is required.
Preference will be given to applicants with experience in an environment under NRC or agreement state regulations. NRRPT certification or eligibility for certification is highly desired. The incumbent must have significant knowledge in a research and development environment with experience in at least one other ES&H discipline, i.e., industrial hygiene, hazardous material handling, biosafety, or industrial safety. The incumbent should be trained in shipping Class 7 materials under both DOT and IATA. In addition, applicants with experience handling transuranic isotopes will be given preference.
Work is performed in a variety of settings including office and laboratory environments, as well as in outdoor areas. Will frequently stand, walk, sit, kneel, crawl, climb (ladders, scaffolds, etc.), reach/work overhead, frequently lift/carry/push/pull heavy objects that weigh up to 50 pounds and perform desk-based computer tasks. Will wear personal protective equipment which may include a respirator. Will work in close proximity to an environment containing research animals and will be required to work in areas where hazardous materials and/or infectious agents are present which may require vaccinations.The above is intended to describe the general requirements for the position and should not be interpreted as an exhaustive statement of physical requirements. The Institute will provide reasonable accommodation to any employee with a disability who requires an accommodation to perform the essential functions of the position.
Salary is commensurate with experience.
Lovelace Biomedical is an Equal Opportunity Employer
Building on a history of pioneering science and technological innovation, Lovelace Biomedical is a contract research organization that helps pharmaceutical and biotechnology companies advance their discoveries—no matter how complex—into clinical testing and beyond. The organization leverages a multidisciplinary toolset to push the limits of preclinical research and fully understand the behavior of its clients’ investigational products. Lovelace Biomedical provides a unique experimental breadth and logistical capacity to solve specialized challenges that other CROs are not equipped to handle, featuring expansive bio-secure facilities and ongoing access to industry-leading scientific experts. The team thrives on developing programs for complex diseases, emerging drug classes and delivery mechanisms, and challenging areas of drug development while delivering the same level of rigor and attention to seemingly straightforward studies that are just as critical to regulatory success.
