Clinical Lab Specialist

Modena Allergy + Asthma•San Diego, CA

12d•$45 - $60•Onsite

About The Position

Modena Health (“MH”) and Modena Allergy & Asthma ("MAA") are leading and rapidly growing medical practices specializing in allergy, asthma, and immunology care, with clinics across Southern California and Arizona—and ambitious plans for national expansion. We are physician-led, hospitality-focused, and technology-enabled, committed to transforming allergy care while advancing clinical research and expanding access to cutting-edge medicine. Known for our high standard of excellence, we provide compassionate, patient-centered care for both pediatric and adult patients. Our model combines hospitality-driven service with innovative technology solutions that streamline operations, improve clinical outcomes, and enhance the experience for both patients and providers. At Modena, we aim to hire great people, treat them well, and help them find meaning and purpose in our mission. Our dedicated team values collaboration, positivity, and growth while striving to improve lives through expert diagnosis, treatment, and research. We are looking for high-energy, kind, and collaborative individuals eager to grow personally and professionally while making a meaningful impact in the lives of others. Position Summary The Clinical Laboratory Scientist (CLS) / Radiopharmacy Technician supports the manufacturing, compounding, and quality control of clinical and radiopharmaceutical products in compliance with State and Federal regulations. This role works closely with cross-functional teams to ensure safe, accurate, and timely production while maintaining strict quality and compliance standards. This is a role well suited to an ambitious professional, looking for the next step in their career.

Requirements

Bachelor’s degree in Clinical Laboratory Science, Chemistry, Biology, or related field (required)
Coursework must include: 16 semester hours of chemistry, including analytical and biological chemistry.
16 semester hours of biological sciences, including microbiology, hematology, and immunology.
3 semester hours of physics, math, or statistics.
Experience working in a sterile or clean room laboratory/environment.
CLS license or applicable laboratory certification (required based on state regulations)
Analytical Chemistry Equipment and Processes (HPLC, GC, TLC)
Strong attention to detail and ability to follow SOP-driven processes
Detail oriented and have strong critical thinking skills.
Work well independently.
Basic computer skills such as spreadsheet, word processing and e-mail.
Strong verbal and written communication skills.
Willing to work night shifts and alternating shifts as needed.

Nice To Haves

Experience in clinical laboratory, radiopharmacy, or regulated manufacturing environments preferred
Hands-on experience with analytical instrumentation (TLC, HPLC, GC) preferred

Responsibilities

Perform testing in areas such as: Allergy testing, Clinical chemistry (e.g., metabolic panels, enzyme assays), Hematology (CBCs with no manual differentials).
Perform complex compounding and manufacturing activities, including cyclotron operation and chemistry module operation, under supervision as required by State and Federal law
Execute quality control testing using analytical equipment such as TLC, HPLC, and GC
Participate in complex inspections, maintenance, and troubleshooting to support manufacturing and testing equipment
Implement approved SOP updates related to production and quality control processes
Conduct Daily, Weekly, Monthly, and Quarterly Preventive Maintenance (PM) checks on: Cyclotrons, Chemistry Modules, Quality Control (QC) equipment, in accordance with established SOPs
Support logistics and distribution activities, including: Preparing products for shipment, Coordinating courier schedules, Completing required documentation and records
Conduct laboratory tests on blood, tissue, and other specimens
Operate and maintain clinical lab equipment
Report and validate test results used by physicians for diagnosis and treatment
Adhere to all cGMP, cGLP, CLIA, CAP, and regulatory requirements (State, Federal, and accrediting bodies)
Maintain accurate and complete batch records, QC documentation, and logs
LIS build and LIS maintenance
Support internal audits, inspections, and corrective actions as needed