Technical Writer

Kelly® Science & Clinical is seeking two experienced Technical Writers for a 6-month contract opportunity with a leading molecular diagnostics company at their headquarters in Sunnyvale, CA. If you are driven by the prospect of translating cutting-edge scientific discoveries into tangible advancements and are poised to advance your career, join us as we pioneer progress in the biotechnology industry.

Workplace: Hybrid based in Sunnyvale, CA (3 days/week in the office)

Position Title: Technical Writer

Position Type: 6-month contract

Pay rate: $45-55/hour

Company: Kelly® Science & Clinical

Overview

The Technical Writer will be responsible for writing, editing, formatting, managing the publication, and overseeing the translation of customer-facing documents for our client’s in vitro diagnostic tests and instrument systems. Document types include Instructions for Use (IFUs), Quick Reference Instructions, User’s Guides, and Getting Started Guides.

Responsibilities

• Create, edit, and publish IFUs, Quick Reference Instructions, and abbreviated IFUs for our clients’ tests.
• Develop User Guides, Getting Started Guides, and service manuals for our client’s instrument systems.
• Conduct reviews and peer reviews of all publications to ensure content accuracy, formatting, and adherence to an internal style guide.
• Initiate and follow up on document reviews with subject matter experts (SMEs).
• Manage translations with third-party vendors and adjust the formatting of translated documents if required.
• Coordinate the release of reviewed publications with the internal document control system.

Qualifications

• Bachelor’s degree in Life Sciences with at least 5 years of relevant work experience.
• Working knowledge of topic-based writing styles.
• Expertise in preparing images for use in documentation.
• Proficiency in English grammar and punctuation, along with strong overall writing skills.
• Experience creating and editing XML files using a Darwin Information Typing Architecture (DITA) Component Content Management System (CCMS), Adobe FrameMaker, Adobe Acrobat, Adobe Illustrator, Adobe Photoshop, Microsoft Word, and Adobe InDesign.
• Basic understanding of regulatory affairs concepts, guidelines, and regulations governing the development, documentation, and labeling of in vitro diagnostic products.
• Strong verbal communication skills for effective teamwork.
• Excellent organizational skills with keen attention to detail and accuracy.
• Ability to prioritize, multi-task, and manage workload efficiently.
• Capacity to maintain a sense of urgency when required by specific events.

Preferred Experience

• Experience developing DITA styling for online user documents.
• Capability to modify Cascading Style Sheets (CSS) for better output styling.
• Experience in medical equipment writing.

Why Join Us

Competitive compensation package and potential for permanent placement following the temporary period.Opportunity to work at the forefront of biotechnology innovation in a collaborative and dynamic environment.Access to ongoing career development and networking opportunities through Kelly® Science & Clinical's expansive network of industry experts and recruiters.

If your qualifications align with the requirements of this role, we invite you to apply and take the next step in your career journey. Rest assured, even if this opportunity isn't the perfect match, your profile will remain within our network, ensuring you're connected to a wealth of future opportunities in the field of science and clinical research.