Document Control Specialist - GMP/ISO 13485 Expert

JenaValve Technology, Inc. is seeking a Specialist in Document Control for their Irvine, CA office. The candidate will coordinate and maintain document/change control systems in compliance with regulations in the medical device industry. Responsibilities include processing documents, providing training, and ensuring adherence to quality practices. A high school diploma and 3-5 years of relevant experience are required, along with familiarity with ISO 13485 standards and ERP systems. The role emphasizes initiative, attention to detail, and effective communication.
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