SupportFinity™
Overview
We're hiring a Technical Writer to join our team in Tucson. The role involves translating complex technical information into clear, concise documentation while working closely with engineers and product teams to create user manuals, guides, and other technical documents. Location
Tucson, United States Role
Technical Writer – Assay Development Responsibilities
Act as Technical Writer on project teams, attend meetings, and update the supervisor. Involved in the creation, review, revision, and approval of documentation and labeling for Tissue Diagnostics products. Qualifications
Bachelor's degree in a scientific discipline or related technical field. 3–5 years of direct documentation experience in the medical device, software, pharmaceutical, or biotechnology industry. Knowledge of current US and International regulations (e.g., FDA, ISO, IVDD, 21 CFR 11) and control of electronic records. Demonstrable record of working on project teams while managing multiple projects. Experience with international regulatory requirements (preferred). Benefits
Medical insurance – PPO, HMO & Dental & Vision insurance 401(k) plan Employee Assistance Program Long-term disability Weekly payroll Expense reimbursement Online timecard approval Apply
Ready to make an impact?
Apply now and let’s grow together!
#J-18808-Ljbffr
We're hiring a Technical Writer to join our team in Tucson. The role involves translating complex technical information into clear, concise documentation while working closely with engineers and product teams to create user manuals, guides, and other technical documents. Location
Tucson, United States Role
Technical Writer – Assay Development Responsibilities
Act as Technical Writer on project teams, attend meetings, and update the supervisor. Involved in the creation, review, revision, and approval of documentation and labeling for Tissue Diagnostics products. Qualifications
Bachelor's degree in a scientific discipline or related technical field. 3–5 years of direct documentation experience in the medical device, software, pharmaceutical, or biotechnology industry. Knowledge of current US and International regulations (e.g., FDA, ISO, IVDD, 21 CFR 11) and control of electronic records. Demonstrable record of working on project teams while managing multiple projects. Experience with international regulatory requirements (preferred). Benefits
Medical insurance – PPO, HMO & Dental & Vision insurance 401(k) plan Employee Assistance Program Long-term disability Weekly payroll Expense reimbursement Online timecard approval Apply
Ready to make an impact?
Apply now and let’s grow together!
#J-18808-Ljbffr