Research Associate II

4 weeks ago


Los Angeles, California, United States Cedars-Sinai Full time
Job Description

**Job Summary:**

Cedars-Sinai is seeking a highly motivated and detail-oriented Research Associate II to join our team in the Heart Institute. The successful candidate will perform routine and increasingly complex laboratory tasks and procedures, developing technical expertise in one or more areas relevant to research projects.

**Essential Job Duties and Responsibilities:**

  • Conducting routine manufacturing of biologic products, including media preparation, cell culture, cell counting, formulation, centrifugation, and freezing.
  • Independently completing required documentation and guiding other operators on proper cGMP recording of entries and comments on batch records, forms, and protocols.
  • Performing a variety of increasingly complex experimental protocols and procedures and assisting in the design of new complex or unusual protocols and techniques.
  • Keeping accurate and detailed records of experiments and results and assisting in identifying and troubleshooting unexpected results.
  • Preparing technical summaries, protocols, and reports.
  • Ordering laboratory supplies and supporting laboratory operations.
  • Maintaining lab equipment and related records and may coordinate use of lab equipment.
  • Assisting in the operation of specialized equipment, as required by the area of research.
  • Assisting in preparation of data for publication and/or presentation at scholarly meetings.
  • Observing and complying with safety standards and procedures.
  • Orienting research laboratory assistants or lower-level research associates and undergraduate student researchers on day-to-day lab operations and routine procedures.

**Qualifications:**

  • Bachelor's degree in Biomedical Engineering, Biological Sciences, or related field.
  • Two (2) years of laboratory experience.
  • 1-3 years of experience in cGMP/cGTP manufacturing environment in academic/industry setting.
  • Individuals with a scientific background, mammalian cell culture, and cGMP experience needed.
  • Working knowledge of the regulatory requirements (cGMP/cGTP) in the biopharmaceutical, blood, and/or tissue banking industry.
  • Understanding of general research objectives.
  • Familiar with routine laboratory procedures, experimental protocols, and overall lab organization.
  • Applicant must be highly motivated and able to work independently. Must have superior interpersonal, communication, and organization skills and the ability to work across company disciplines and functional units, and computer application experience.
  • Must possess computer skills to include, but not limited to, Excel and Word.
  • Ability to simultaneously manage multiple clerical trials, and attention to details.

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