Research Chemist / Production Associate

MEDICAL ASSETS HOLDING COMPANY LLC•Little Rock, AR

6d•$39,857 - $45,000•Onsite

About The Position

The Quality Control/Production Associate is an entry level position that plays a key role in producing life-changing PET drug products and research materials, ensuring their quality through hands-on work with advanced laboratory equipment and analytical instruments. 3D Imaging is a small contract research company specializing in the production and use of radiopharmaceuticals, primarily for PET scanning. We also operate a medical cyclotron facility producing radiopharmaceuticals for clinical trials and research use. Our clients include pharmaceutical and biotechnology companies, governmental agencies such as NIH, NCTR, and FDA, and investigators at UAMS. Common methodologies include synthetic organic chemistry, inorganic chemistry, and radiochemistry.

Requirements

High School Diploma required
Familiarity with analytical techniques.
Strong organizational skills with data and paperwork.
Excellent problem-solving and written/verbal communication skills.
Willingness to work with radioactive materials and the ability to follow strict safety guidelines.
Proficiency in basic computer applications, including data entry, analysis, and documentation using Microsoft Excel and Microsoft Word.
Ability to be detail-oriented, accountable, patient, organized, and able to work independently or in a dynamic team environment required.
Ability to lift up to 50 lbs.
Willingness to work on a rotating shift schedule
Excellent judgment and discretion: ability to handle multiple priorities simultaneously, meet deadlines, and handle work-related stress professionally is required.
Self-motivated, ambitious professional with the initiative and resilience to master complex, technically demanding tasks. Including operation of complex machinery through structured, hands-on training and progressive responsibility.
Willingness to learn and adapt in a fast-paced, highly technical environment.

Nice To Haves

Associate degree in chemistry, engineering, or sciences preferred.
Bachelor's degree in chemistry, radiochemistry, chemical engineering, or related field.
Experience with coding or scripting (e.g., Python, MATLAB, R, or similar) for process optimization.
Basic mechanical aptitude, including comfort using common hand and power tools for simple assembly or repair tasks.
Introductory knowledge of electrical components or wiring, with an understanding of fundamental safety practices
Knowledge of calibration, operation, maintenance, and repair tasks of basic laboratory equipment such as GC, HPLC, TLC etc.
Experience handling radioactive materials (RAM).
Experience preparing radiolabeled materials and radiopharmaceuticals, including those for human use.
Ability to read, interpret, and communicate technical information from manuals.
Basic cyclotron operation and maintenance and support systems.
Familiarity with cGMP, FDA, or other regulatory standards.

Responsibilities

Perform FDG synthesis according to 3D Imaging SOPs
Ensure all materials and reagents are received and verified according to SOPs and cGMP standards
Perform routine operation of the remote/automated FDG synthesis system, including setup, reagent loading, process monitoring, and documentation, to ensure consistent production of clinical-grade [¹⁸F]-FDG.
Operate, monitor, and document cyclotron and/or synthesis activities under supervision, as applicable.
Conduct in-process checks and assist with quality control sampling and testing (e.g., dose calibrator measurements, pH, visual inspection).
Complete batch records and manufacturing documentation accurately.
Perform cleaning, environmental monitoring support, and routine maintenance of hot cells, equipment, tools, laminar flow hoods, and production areas.
Adhere strictly to radiation safety, aseptic technique, and regulatory compliance standards.
Package, label, and prepare finished doses for distribution.
Report deviations, equipment issues, or out-of-specification results promptly to supervision.