Document Control Specialist

Title

Technical Document Control Coordinator

Miami, FL 33196

10+ Months (Extendable)

$25.00 - $27.79/hr on W2

$25.00/hr - $27.79/hr

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.

• 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.

• 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.

• Knowledge/Experience of medical device quality systems including FDA, GMP & ISO preferred.
• Knowledge of 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.

• Associate

• Contract

• Writing/Editing and Analyst

• Medical Practices and Medical Equipment Manufacturing