Biomedical Specialist

Biomedical Specialist Cedars-Sinai - 4.1 West Hollywood, CA Job Details $77,022.40 - $119,392.00 a year 5 hours ago Qualifications Bachelor's degree Full Job Description Job

ID 16147

Location West Hollywood, California, United States Job Category Academic / Research Date posted 05/01/2026 Job Description Grow your career at Cedars-Sinai! Cedars-Sinai Medical Center has been named to the Honor Roll in U.S. News & World Report's "Best Hospitals 2025-2026" rankings (opens in new window) . When you join our team, you'll have access to groundbreaking biomedical research facilities and world-class medical education programs. We take pride in hiring exceptional, dedicated professionals who are passionate about advancing healthcare. Our physicians, nurses, and staff reflect the culturally and ethnically diverse communities we serve and are united by a shared commitment to excellence. Together, we foster a dynamic, inclusive environment that drives innovation and supports the gold standard of patient care. Are you ready to be a part of breakthrough research? The Cedars-Sinai Biomanufacturing Center (CBC) is a state-of-the art facility that comprises of a cGMP cell manufacturing facility housing multiple cleanroom cell production suites and process development rooms for producing the next generation of cell and gene therapies. With world class expertise in stem cell (iPSC) biology, bioprocessing, translational, regulatory and manufacturing, Cedars-Sinai is committed to pushing the frontiers of medicine and discovering new technologies and innovations that will impact how we diagnose and treat disease. To learn more about the CBC, please visit: Home - CSBIO (csbiomfg.com) (opens in new window) The Biomedical Specialist participates in project development for multiple projects. Performs process development, validation, qualification tasks associated with the project. May be responsible for writing or aiding in the writing of SOPs for the project. Performs project-related techniques in accordance to established standard operating procedures (SOP) with accurate documentation and assists cross functional teams with required activities. Proactively completes assigned projects, and uses advanced knowledge and experience to independently conduct, analyze and report studies. Will be expected to provide communication, guidance, and advice that contributes to the success of projects. Trains entry level staff project related activities. Performs routine and increasingly complex laboratory tasks and procedures and develops technical expertise in one or more areas relevant to research projects. Responsibilities include ordering and maintenance of lab equipment, and vendor management. Participates in research activities involving all aspects of the research or protocol process, including investigation, technical, testing/validation of results, and report findings. Primary Duties and Responsibilities Performs a variety of QC functions in support of cGMP aseptic Biological Drug manufacturing and process development. QC testing will vary for each project based on the type of cells, tissues or organs. Performs a broad range of tissue culture and microbiological methods, utilizing good aseptic techniques and lab practices in support of for developing, processing and manufacturing both research and clinical grade cellular products in accordance to established standard operating procedures (SOP). Performs cellular, micro- and molecular biology procedures including, but not limited to Western blot, Northern blot, DNA / RNA, Polymerase chain reaction (PCR), Flow cytometry, Gene expression analysis, protein extraction, cell culture, immunocytochemistry, and staining. Expected to execute environmental monitoring (EM), QC analysis, provide technical oversite and complete routine record review of test data and related GMP documents under minimal supervision. Will conduct investigations regarding EM action level excursions and out of specification (OOS) results for any QC-tests executed within the CBC or by external laboratories. Will develop, revise and review SOPs, and monitor GMP systems currently in place to ensure compliance with documented policies. Must also have the ability to perform statistical analysis to generate trend reports on environmental monitoring and product release data. Handwriting must be legible. Knowledgeable in molecular biology techniques including m

RNA, DNA

extraction, RT-PCR, PCR, expression analysis. Maintains compliance with established laboratory SOPs, GMP, MTA's and safety procedures Must be well-organized, detail-oriented with meticulous record keeping and a desire to ensure accurate results. Will train new staff on environmental monitoring, analytical and retain samples inventory management and analytical techniques when needed.

Qualifications Education:

Bachelor's Degree in biology, biochemistry, or related science or engineering specialization .

Experience and Skills:

2 years' experience working in a laboratory or biomedical/biotech field. 2 years' experience with biomedical equipment such as maintenance and/or testing. Experience with genus and species identification of various microbes, applying GMP in QC Lab, implementing CAPA and initiating change control is desirable is highly desired. Experience with maintenance of analytical and retain sample inventory logs under GMP compliance is a plus. Demonstrated ability to apply cGMP knowledge to write procedures and manage projects. Prior experience working in an aseptic environment, biosafety cabinet and working with human and animal tissues. Req

ID 16147

Working Title Biomedical Specialist - Biomanufacturing Facility Department CS Biomanufacturing Facility Business Entity Cedars-Sinai Medical Center Job Category Academic / Research Job Specialty Biomanufacturing Overtime Status EXEMPT Primary Shift Day Shift Duration 8 hour Base Pay $77,022.40 - $119,392.00 Diversity and Inclusion at Cedars-Sinai We are caretakers and innovators committed to the pursuit of equitable healthcare. But health equity is not possible without representation. Our commitment to diversity goes beyond demographics or checking boxes. Our people must reflect the diverse identities, experiences and geographies of the communities and patients we serve - because that's what our patients, colleagues and communities deserve Quality Care and Research—For All, By All . Cedars-Sinai is an Equal Employment Opportunity employer. Cedars-Sinai does not unlawfully discriminate on the basis of the race, religion, color, national origin, citizenship, ancestry, physical or mental disability, legally protected medical condition (cancer-related or genetic characteristics or any genetic information), marital status, sex, gender, sexual orientation, gender identity, gender expression, pregnancy, age (40 or older), military and/or veteran status or any other basis protected by federal or state law. If you need a reasonable accommodation for any part of the employment process, please contact us by email at and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address. Cedars-Sinai will consider for employment qualified applicants with criminal histories, in accordance with the Los Angeles Fair Chance Initiative for Hiring. At Cedars-Sinai, we are dedicated to the safety, health and wellbeing of our patients and employees. This includes protecting our patients from communicable diseases, such as influenza (flu). For this reason, we require that all new employees receive a flu vaccine based on the seasonal availability of flu vaccine (typically during September through April each year) as a condition of employment, and annually thereafter as a condition of continued employment, subject to medical exemption or religious accommodation. For the same reason, you may also be required to receive other vaccines as a condition of employment. Cedars-Sinai reserves the right to make modifications to its required list of vaccines as required by law and/or policy.