Manage documentation changes in a highly regulated environment, including updates to BOMs, routers, and manufacturing procedures, ensuring compliance with quality and regulatory standards.

Job Requirements:

  • Bachelor's degree
  • 5+ years of experience in a manufacturing or automated environment
  • Experience with creating documentation changes in a highly regulated industry (Medical Device)

Preferred Skills:

  • Experience with Change Orders and Quality documentation
  • Knowledge of BOMs (Bill of Materials), routers, and manufacturing procedures
  • Familiarity with regulatory compliance in a manufacturing setting

Job Responsibilities:

  • Manage and implement changes to BOMs, routers, and manufacturing procedures
  • Create and maintain documentation changes in compliance with regulatory requirements
  • Oversee Change Orders and ensure all quality documentation meets standards
  • Collaborate with cross-functional teams to ensure smooth implementation of manufacturing changes in an automated environment


Pay Details: $40.00 to $50.00 per hour

Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.

Equal Opportunity Employer/Veterans/Disabled

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The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:
  • The California Fair Chance Act
  • Los Angeles City Fair Chance Ordinance
  • Los Angeles County Fair Chance Ordinance for Employers
  • San Francisco Fair Chance Ordinance
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