Seeking a Technical Writer- Assay Development for a long-term contract in Tucson, AZ, with pay at $27/hr on W2.
Responsibilities include creating, editing, and maintaining technical documentation for diagnostic products, collaborating with R&D, Quality, and Regulatory teams to ensure compliance with FDA, ISO 13485, and 21 CFR Part 11 standards.
Support SOPs, work instructions, manuals, and labeling content; participate in document reviews, change control, and audits.
Qualifications include 3–5 years of biotech or medical device writing experience, strong knowledge of regulatory standards, proficiency with electronic document control systems, and a Bachelor's degree in a related science field.
Benefits include medical, dental, vision, paid sick leave, and 401K.
Interested candidates should send their resume to hr@dawarconsulting.com.