Biomedical Scientist – Manufacturing

Requisition # HRC0769065

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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: Biomanufacturing Services | Cedars-Sinai (

The Biomedical Scientist leads project development and compliance of all Federal and State accrediting agency including the Food and Drug Administration (FDA) requirements in good manufacturing practices (GMP) for cellular products in the CBC. As a Biomedical Scientist, perform process development, validation, and qualifications for cellular production in GMP / good laboratory practice (GLP) environment while providing guidance, technical expertise, and evaluating client processes to make recommendations for improvement. In this role, the Biomedical Scientist supervises a production team, tissue culture techniques, aseptic technique, and writing standard operating procedures (SOPs) for developing and processing clinical grade and research grade cellular products. Responsible for managing assigned projects and managing associates activities in regulated working environment, writing and recording controlled documents for assigned projects, and coordinating in assisting quality control team with all required testing activities. Provides excellent communication and must have an in-depth understanding of laboratory and research functions to ensure the success of projects.


Primary Duties & Responsibilities:

  • Supervises and performs a variety of cGMP manufacturing production and process development projects for multiple clients following standard operating procedure for manufacturing processes that will be different for each project based on the type of cells, tissues or organs.
  • Assists with cGMP manufacturing schedule and drafts overall timeline for projects as reference for finalizing manufacturing productions.
  • Finalizes cGMP manufacturing production and process development reports and maintains computer database.
  • Leads projects, trains and assists other manufacturing associates on day-to-day lab operations and procedures. Monitors performance, completes performance appraisals, and addresses performance issues. Performs and trains associates on all cGMP/ GLP related activities.
  • Ensures all activities comply with regulatory guideline and safety standards by monitoring all ongoing activities and interacts regularly with QA and Regulatory Affairs.
  • May develop hypothesis and assist in planning steps for the investigative process, reviewing and remaining current on literature as it relates to clinical/research study.

Department-Specific Responsibilities:

  • Supervises a laboratory or program with authority to make decision relevant to those programs.
  • Performs tasks related to the project and plans tasks, assigns work, monitors work, and identifies issues/problems, and makes plans to resolve problems.
  • Assists with the scheduling of resources and drafts overall timeline for projects.
  • Prepares written and verbal updates and findings, including slide presentations, and presents project updates.
  • Performs and maintains good documentation practices, and ensures all documentation adheres to Federal and State accrediting agency requirements, including FDA requirements as necessary.
  • Writes and reviews SOPs and maintains computer database of established protocols.
  • Maintains electronic and non-electronic records and adheres to GLP practices.
  • Identifies and responds appropriately to both internal and external customer needs utilizing available resources
  • Collaborates to problem solve and make decisions to achieve desired outcomes
  • Establishes effective working relationships with cross-functional team(s).
  • Responds timely, effectively and appropriately to deliverables
  • Shares knowledge, time and expertise to assist other members of the team
  • Supervises the day-to-day work of employees, assigns work, ensures tasks are completed and deadlines are met.
  • Responsible for hiring, onboarding, managing schedules, personnel actions, performance reviews, and performance improvement plans.


  • Bachelor’s Degree in molecular biology, biochemistry or related science/engineering field required. Master’s or Doctoral degree, preferred.

Experience and Skills:

  • Eight (8) years experience in GMP/GLP or equivalent regulated facility. Scientific experience is a plus.
  • Must have experience working in an aseptic environment, a biosafety cabinet and experience working with human and animal tissues.
  • Ability to apply critical thinking to analyze and interpret information and/or data.
  • Ability to convey and/or receive written/verbal information to/from various audiences in different formats.
  • Ability to provide and/or support a level of work excellence and accuracy; recognize and address flaws or errors that others may overlook.
  • Ability to apply advanced knowledge of science/learning/specialized intellectual instruction to analyze, interpret or make deductions from varying facts or circumstances.
  • Ability to operate mechanical/medical devices and/or equipment.
  • Ability to apply knowledge of information software and/or hardware to provide solutions and/or support.
  • Ability to handle multiple demands and/or manage complex and competing priorities.
  • Ability to motivate, monitor, measure, recognize and improve performance and morale.
  • Working Title: Biomedical Scientist – Manufacturing – Biomanufacturing Center
  • Department: CS Biomanufacturing Facility
  • Business Entity: Academic / Research
  • City: Los Angeles
  • Job Category: Biomanufacturing
  • Job Specialty: Biomanufacturing
  • Position Type: Full-time
  • Shift Length: 8 hour shift
  • Shift Type: Day

Cedars-Sinai is an EEO 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) and COVID-19. 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 such as COVID-19 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.

Job Type: Full Time

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