Job Title : Document Control Coordinator.Duration : 10 Months+ (Possible Extension).Shift : Monday - Friday 8 am – 5 pm.As a Technical Documentation Coordinator Contractor, you will, create, for...Show moreLast updated: 3 hours ago
Technical Document Control Coordinator
Sunrise Systems, Inc.Miami, FL
Temporary
Quick Apply
Medical Device Manufacturing Company.Technical Document Control Coordinator.This is for an initial duration of.Job Title : Technical Document Control Coordinator.
Position Type : Hourly Contract Posit...Show moreLast updated: 1 day ago
Promoted
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New!
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LHH USMiami, FL, US
Full-time
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Promoted
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Full-time
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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