Technical Writer - Assay Development

The primary responsibility of this position is to act as the Technical Writer on project teams, attend meetings, and update the supervisor. Involved in the creation, review, revision and approval of documentation and labeling for Roche Tissue Diagnostics products.

SKILLS, EXPERIENCE & EDUCATION

3-5 years of direct documentation experience in medical device, software, pharmaceutical, or biotechnology industry

Knowledge of current US and International regulations as they pertain to documentation (e.g., FDA, ISO, IVDD and 21 CFR 11), and control of electronic records

Demonstrable record of working on project teams while working on multiple projects

Experience with international regulatory requirements (preferred)

Bachelor's degree in a scientific discipline or other related technical field

Nesco Resource offers a comprehensive benefits package for our associates, which includes a MEC (Minimum Essential Coverage) plan that encompasses Medical, Vision, Dental, 401K, and EAP (Employee Assistance Program) services.

Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.

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