Location: Local candidates preferred–Minneapolis, MN (however, will consider remote)

Duration: 12 months

POSITION DESCRIPTION

 This position will be responsible for ensuring quality and consistency in labeling and related technical documents. Help to align labeling with standard guidelines and documented procedures for master branding, medical device labeling regulations and standards, meeting all requirements as defined in labeling attributes master plans and product specifications.

 PRIMARY RESPONSIBILITIES

  • Executing editorial standards.
  • Edit medical device labeling according to defined internal and external standards.
  • Proofread English material; check grammar, spelling, consistency, clarity and compliance with internal and regulatory labeling requirements.
  • Conduct quality check of multi-lingual labeling content to identify lack of consistency or irregularities in content.
  • Provide substantive editing and proofreading for product labeling (e.g., product and package labels, product inserts, carton artwork, etc.) and documentation.
  • Acquire and utilize product knowledge by working with labeling specialists, labeling designers, product developers, regulatory, quality, and marketing personnel and by referring to the product, the technical specifications and engineering documentation, and medical device standards and regulations.
  • Maintain necessary records for project tracking and quality requirements.
  • Collaborate and communicate with team members to ensure timely completion of projects.
  • Provide input regarding labeling content.

 REQUIRED QUALITIFCATIONS

  • Requires a University Degree and 2–4 years’ experience in editing, proofreading or technical editing or related field.
  • Ability to handle multiple projects on an ongoing basis.
  • Exceptional attention to detail.
  • Ability to work independently, prioritize and meet deadlines.
  • Ability to edit the work of others and provide feedback in a clear, effective, and positive manner.

DESIRED/PREFERRED QUALIFICATIONS

  • Experience in proofreading/editing labeling content for the medical device. industry or regulated environment.
  • Knowledge of medical terminology.
  • Knowledge of document management systems (e.g., Agile, Documentum, eMatrix).

Location: Prefer local candidates—Minneapolis;  however, will consider remote

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