Actalent
Job Title
Technical Writer Job Type & Location
Permanent – Irvine, California Pay and Benefits
Salary $59,280 – $74,880 per year. Health plans, retirement 401(k), life insurance, paid time off. Additional employee discounts on dental products, cafeteria, gym, and entertainment. Responsibilities
Deliver high‑quality documentation and in‑product text updates. Generate protocols, technical reports, test methods, and manufacturing instructions. Create, update, and maintain design history files and technical submission files. Revise and update instructions for use (IFUs), manuals, brochures, and other documentation. Coordinate with the regulatory team on technical file submissions and approval processes. Essential Skills
Technical writing with FDA regulatory knowledge. Strong writing, in‑product text editing, and documentation processes. Experience in the medical device industry and with BOM, design history files. Additional Skills & Qualifications
Minimum three years of direct documentation experience in manufacturing or related industry. Familiarity with the dental industry is preferred. Knowledge of ISO 9001 and Lean Six Sigma certification. Understanding of the 5 Y’s methodology. Work Environment
Startup culture with flexibility, fast‑moving priorities. Engineers work on projects 9–10 months before reassignment. Family‑friendly, diverse environment with philanthropic events, sports matches, and holiday celebrations. Application Deadline
October 28, 2025. Equal Opportunity Statement
Actalent is an equal‑opportunity employer. We consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. For reasonable accommodation, email actalentaccommodation@actalentservices.com.
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Technical Writer Job Type & Location
Permanent – Irvine, California Pay and Benefits
Salary $59,280 – $74,880 per year. Health plans, retirement 401(k), life insurance, paid time off. Additional employee discounts on dental products, cafeteria, gym, and entertainment. Responsibilities
Deliver high‑quality documentation and in‑product text updates. Generate protocols, technical reports, test methods, and manufacturing instructions. Create, update, and maintain design history files and technical submission files. Revise and update instructions for use (IFUs), manuals, brochures, and other documentation. Coordinate with the regulatory team on technical file submissions and approval processes. Essential Skills
Technical writing with FDA regulatory knowledge. Strong writing, in‑product text editing, and documentation processes. Experience in the medical device industry and with BOM, design history files. Additional Skills & Qualifications
Minimum three years of direct documentation experience in manufacturing or related industry. Familiarity with the dental industry is preferred. Knowledge of ISO 9001 and Lean Six Sigma certification. Understanding of the 5 Y’s methodology. Work Environment
Startup culture with flexibility, fast‑moving priorities. Engineers work on projects 9–10 months before reassignment. Family‑friendly, diverse environment with philanthropic events, sports matches, and holiday celebrations. Application Deadline
October 28, 2025. Equal Opportunity Statement
Actalent is an equal‑opportunity employer. We consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. For reasonable accommodation, email actalentaccommodation@actalentservices.com.
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