Job Description :

Greetings,

 

Got your profile from Job Board. Looking at your profile I could find out you have some great experience as Technical Writer

We do have an opportunity, which I would like to discuss with you. 

 

Position: Technical Writer (Experience with FDA regulatory compliance)

Location: Santa Clara CA (Initial Remote) - Local to CA

Employment type: C2C

Duration: 6 months.

 

Experience: Min 9+ year’s profile

 

 Required:  

  • Support development processes and tool integration
  • Identify and escalate potential document generation improvements 
  • Identify process gaps and potential inefficiencies, articulate and recommend potential improvements.
  • Describe, in translatable English, complex processes.
  • Work with multi-disciplinary project team members to produce and maintain world-class project
  • Documentation deliverables (DHF) through providing hands-on examples.
  • Write for a variety of audiences, from non-technical end users to software engineers and regulatory bodies (such as FDA).
  • Monitor metrics on the quality of the produced documentation as well as identifying and implementing improvements to the documentation process.
  • Seek to refine process descriptions, to arrive at succinct, concise descriptions – avoiding verbose and dense demonstrations of pedantic prose.

Requirements 

  • Strong understanding of Quality Management Systems (QMS) and regulations (IVDR, 21CFR820)
  • Strong understanding of Standalone Software, especially in to regulations, design,
  • Development, and auditable artifacts.
  • Associate’s Degree, or equivalent combination of education and work experience
  • 3+ years of technical writing experience. 
  • Strong written and verbal communications and experience working with content in multiple mediums.
  • Experience working with the following tools preferred: Confluence/JIRA, Git/Github, Microsoft
  • Office suite, Google Docs/Spreadsheet/Slides, IntelliJ.
  • Knowledge of relevant international ISO Standards (ISO 13485, 14971, 62304)
  • 3+ years of experience within a Regulated Industry (medical device / pharma preferred.)

If Interested please reply with below details

·         Updated Resume

·         Best time to talk

·         Number to connect

Yogesh Kadam

Nityo Infotech



Client : Nityo Infotech

             

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