The Planet Group
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http://www.theplanetgroup.com
http://www.theplanetgroup.com
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Technical Writer
12390 El Camino Real San Diego, CA 92130 US
Posted: 08/28/2023
2023-08-28
2023-10-21
Employment Type:
Contract
Job Category: Technology
Job Number: 578013
Country: United States
Is job remote?: No
Job Description
Technical Writer
Location: Minneapolis, MN or San Diego, CA; Onsite
Pay: up to $55 per hour DOE
Benefits: Health, Dental, Vision and more
Job Overview:
Planet Technology's client is seeking Technical Writers. You will be responsible for document content creation and reformatting existing documents to support harmonization activities within the quality management and other related projects. This position will be part of the quality organization and assist in providing support to other functional areas as necessary.
Job Responsibilities:
Must Haves:
Nice to Haves:
Location: Minneapolis, MN or San Diego, CA; Onsite
Pay: up to $55 per hour DOE
Benefits: Health, Dental, Vision and more
Job Overview:
Planet Technology's client is seeking Technical Writers. You will be responsible for document content creation and reformatting existing documents to support harmonization activities within the quality management and other related projects. This position will be part of the quality organization and assist in providing support to other functional areas as necessary.
Job Responsibilities:
- Exceptional writing, communication, and organizational skills.
- Ability to write clear, simple content that can be readily understood at all levels within the organization.
- Strong attention to detail and proofreading skills
- Collaborate openly and effectively with a range of stakeholders, including subject-matter experts
- Help other writers in creating documentation
- Basic understanding of regulatory compliance for medical devices or pharmaceuticals
Must Haves:
- Minimum of four years of college or equivalent work experience
- Minimum of 2 years’ experience as a technical writer
- Minimum 2 years’ experience working in medical device or pharmaceutical industry
- Experience with eQMS software for document control (Familiarity with MasterControl a plus)
- Fluent with Microsoft Office business software, particularly Microsoft Word, Excel and PowerPoint
- Knowledge of GMP, ISO, QSR and other applicable international standards, regulations, directives and guidance
Nice to Haves:
- Familiarity with MasterControl a plus
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