TECHNICAL WRITER / PROOFREADER - Sarkari and Private Naukri

Sarkari and Private Naukri

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Friday, February 14, 2020

TECHNICAL WRITER / PROOFREADER

          TECHNICAL WRITER / PROOFREADER

Job Description

 
About the role
Under the direction of the COE Graphics and Labeling (G&L) Leadership team and/or team lead, the Technical Writer/Proofreader will review files to ensure consistency and accuracy in spelling, grammar, punctuation, content, layout, writing, documentation research and compliance, as well as applying brand and corporate identity standards.
Principal Accountabilities
  • Proofread new and updated labeling and packaging documents to ensure that all required changes have been accurately completed. Write and review content for grammar, spelling and capitalization. Ensure that brand and Corporate Identity standards have been met.
  • Compile any corrections, changes, errors or inconsistencies using Adobe Acrobat and Microsoft Excel.
  • Effectively use Corporate Identity reference guides to ensure consistency throughout all materials.
  • Proofread against redline change requirements. Ã¢€¨
  • Work cooperatively with the team to meet all specified deadlines.
  • Labeling and Packaging experience with understanding of brand management strongly preferred.
  • Proficient in Microsoft Excel and Adobe Acrobat. AutoCad knowledge is a plus.
  • Must have knowledge of standard proofreader marks and sentence structure.
  • Must be highly detail-oriented with a strong eye for catching mistakes.
  • Must be highly organized and be able to work on multiple projects simultaneously. 
  • Possess excellent communication and interpersonal skills to work effectively within a cross-functional project team.
 Required Candidate profile
Qualification
Associate or Bachelor Degree equivalent in English, Communications, Journalism, Marketing or related field.
Experience
A minimum of 3 years of writing, proofreading, editing and documentation experience in the Medical/Healthcare Industries.
Special Skills:
 Working knowledge of Adobe Creative Suite, a plus
  • Medical Device experience a plus.
  • American English Knowledge.
  • Multilingual a plus.
 Knowledge of Specific Procedures and Practices:
 External Regulations (ISO, FDA, OSHA, ASTM), EUMDR/IVDR, Brexit, UD.


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