Technical Writer
at Labstat International Inc
Kitchener, ON, Canada -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 26 Nov, 2024 | Not Specified | 29 Aug, 2024 | 2 year(s) or above | Software,Technical Writing,Completion | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
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