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Senior Analyst, Standards Specialist

Johnson & Johnson · New Brunswick, NJ +4 more

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QualityFull-time$94k–$152kCompany career page

The apply link worked recently (not employer-confirmed).

Role summary

Johnson & Johnson seeks a Senior Analyst, Standards Specialist to manage enterprise quality standards revisions and updates within the Regulatory Compliance organization. The role involves coordinating document workflows, partnering with subject matter experts, maintaining program metrics, and implementing continuous improvements across multiple facility locations.

What they're looking for

  • Bachelor's degree in life sciences, quality, regulatory affairs, engineering, or related field
  • At least five years of quality experience in a regulated industry
  • Experience with controlled-document authoring, revision, and approval workflows
  • Knowledge of quality system documentation concepts and GxP/medical device requirements
  • Strong facilitation and stakeholder coordination skills in matrixed environments
  • Proficiency with document management systems like Veeva and Excel data analysis
  • Excellent written communication and attention to detail

What you'll be doing

  • Coordinate end-to-end revisions of enterprise quality standards, including intake, tracking, and governance review preparation
  • Partner with sector subject matter experts to facilitate content updates and implement changes
  • Route standards through document management systems for review and approval according to procedures
  • Maintain program metrics, dashboards, and periodic review calendars to track efficiency and identify improvements
  • Support environmental scans and continuous improvement initiatives to enhance the standards program

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