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Manufacturing Associate I/II

CAPRICOR THERAPEUTICS, INC

Manufacturing Associate I/II

Los Angeles, CA
Full Time
Paid
  • Responsibilities

    POSITION: Manufacturing Associate I/II

    This position is immediately available to join our Manufacturing team to perform cGMP manufacturing to support Capricor’s clinical trials and exosome development. Capricor is developing its exosome technology as a next-generation therapeutic platform. The Company’s current focus is on developing exosomes capable of delivering nucleic acids, including mRNA as well as proteins, to treat or prevent a variety of diseases.  We are seeking an individual with a scientific background, mammalian cell culture and cGMP experience.

     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
    • Compiling data for documentation of test procedures and reporting abnormalities
    • Making detailed observations, planning and assisting with data collection, data analysis, writing and disseminating production results
    • Authoring, revising and updating standard operating procedures using the document change system
    • Maintaining broad knowledge of state-of-the-art principles and theories
    • Maintaining inventory, material transfers and cleanroom-required activities to support cGMP operations
    • Preparing technical summaries, protocols and reports
    • Initiating and closing deviations, investigations and CAPAs of moderate complexity; and
    • Performing special manufacturing and development projects

    REQUIREMENTS:

    • Bachelor’s degree in Biomedical Engineering, Biological Sciences or related field
    • 1-3 years of experience in cGMP/cGTP manufacturing environment in academic/industry setting
    • Laboratory experience in mammalian tissue culture is required
    • Working knowledge of the regulatory requirements (cGMP/cGTP) in the biopharmaceutical, blood and / or tissue banking industry
    • Exceptional communication and interpersonal skills
    • Excellent organizational skills and attention to detail
    • Ability to work in a dynamic environment
    • Adaptable/flexible with work schedule with an ability to multi-task and prioritize work
    • Basic molecular biological and flow cytometry skills are preferred