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Technical Document Control Coordinator
Technical Document Control CoordinatorSunrise Systems, Inc. • Miami, FL
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Technical Document Control Coordinator

Technical Document Control Coordinator

Sunrise Systems, Inc. • Miami, FL
8 days ago
Job type
  • Temporary
  • Quick Apply
Job description

Our client, a leading Medical Device Manufacturing Company is looking for Technical Document Control Coordinator and This is for an initial duration of 10 Months Contract – Miami, FL

Job Title : Technical Document Control Coordinator

Job Id : 26-00020

Location : Miami, FL

Duration : 10 Months Contract

Position Type : Hourly Contract Position (W2 only)

  • Monday-Friday 8am - 5pm
  • Fully on site

Role

  • As a Technical Documentation Coordinator Contractor, you will, create, format, and coordinate the approval and implementation of labeling documents and reagent and consumable instructions for use documents.
  • This position requires experience with the following :

  • Editing and proofing of English and multilingual Reagent IFU documents.
  • Ensure reagent and instrument labeling documents are created, updated and in compliance with company standards, ISO and GMP as required
  • Creation and maintenance of documentation and illustrations that are used by analytical systems
  • Creation and revision of product labels using Adobe Illustrator or similar graphic tools.
  • Implementation of Design Changes to labeling; release change in compliance with company standards
  • Work with multifunctional teams including Regulatory Affairs, Technical Support and Manufacturing to complete day to day activities.
  • Query business systems for company information to complete the project documentation
  • Follow company process and procedures to schedule and project from draft through approval and release.
  • Participates in team meetings
  • Requirements :

  • Bachelor's Degree preferred with 0-2 years of experience
  • Proficient in Microsoft Office applications, Adobe Acrobat and other design tools such as Adobe Illustrator and Adobe Photoshop.
  • Demonstrated ability to operate independently, with initiative and good business judgment
  • Excellent verbal and written communication skills including grammar
  • Excellent organizational and follow-up skills, as well as great attention to detail
  • Desire to work independently with minimum supervision
  • Can work and communicate effectively with a variety of people and across functional groups.
  • Preferred

  • Knowledge / Experience of medical device quality systems include FDA, GMP & ISO preferred
  • Knowledge computer systems used in product development and manufacturing
  • Ability to coordinate project activities with multiple groups and individuals
  • Prioritize tasks and resolve routine issues.
  • Experience working with labels and multilingual documents
  • Experience working in a fast-paced environment
  • Create a job alert for this search

    Document Control Coordinator • Miami, FL

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