Technical Writer

at  Labstat International Inc

Kitchener, ON, Canada -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate26 Nov, 2024Not Specified29 Aug, 20242 year(s) or aboveSoftware,Technical Writing,CompletionNoNo
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Description:

Certified Group is a leading North American provider of laboratory testing, regulatory consulting, and certification & audit services. Certified Group includes Food Safety Net Services (FSNS), Certified Laboratories, EAS Consulting Group, Labstat International Inc., Advanced Botanical Consulting & Testing (ABC Testing Inc.), Microconsult Inc., and Micro Quality Labs Inc. Certified Group provides laboratory testing and regulatory consulting services in the food & beverage, dietary supplements & NHP, cosmetics, OTC, tobacco, nicotine, cannabis, hemp, and other industries.
We are currently looking for a Technical Writer to join our growing team in Greensboro, North Carolina with our Labstat Division!

MINIMUM QUALIFICATIONS:

  • B.Sc. (Science), preferred
  • Completion of educational program related to Technical Writing
  • 2 Years technical experience
  • Proficiency I technical writing tools and software (e.g., Microsoft Office Suite, Adobe)
  • Experience as a scientific or technical writer, with a strong portfolio of written work.
  • Knowledge of GLP is an asset

Responsibilities:

  • Technical Documentation: Write, edit, and proofread scientific and technical documents, including research papers, technical reports, user manuals, and standard operating procedures (SOPs).

  • Content Development: Develop and maintain documentation standards and guidelines to ensure consistency and clarity across all documents.

  • Research: Conduct thorough research and collaborate with subject matter experts (SMEs) to understand complex scientific and technical information.
  • Data Interpretation: Analyze and interpret scientific data and research findings to accurately represent them in written form.
  • Technical Communication: Simplify and present complex technical information in an accessible and engaging manner for various audiences, including non-technical stakeholders.
  • Review and Revision: Review and revise documents based on feedback from SMEs, peer reviews, and quality assurance checks.
  • Compliance: Ensure that all documentation complies with industry standards, regulatory requirements (GLP), and company policies.
  • Project Management: Manage multiple documentation projects simultaneously, ensuring timely completion and adherence to deadlines.
  • Comply with Health & Safety policies and procedures and wear required Personal Protective equipment at all times
  • Perform other duties as assigned.


REQUIREMENT SUMMARY

Min:2.0Max:7.0 year(s)

Information Technology/IT

Pharma / Biotech / Healthcare / Medical / R&D

Content, Journalism

BSc

Proficient

1

Kitchener, ON, Canada