Intermediate Technical Writer

This job is with Thermo Fisher Scientific, an inclusive employer and a member of my Gwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.

Work Schedule
Standard (Mon-Fri)  Environmental Conditions
Office

Job Description

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

Join a leading scientific organization making meaningful contributions to global health, environmental protection, and food safety. As a Technical Writer III, you'll create clear, concise documentation that enables our customers and internal teams to effectively utilize our products and processes. Working across multiple departments and technologies, you'll translate complex scientific and technical information into user-friendly content that supports our mission of enabling customers to make the world healthier, cleaner and safer.

You'll collaborate with subject matter experts, engineers, scientists, and quality teams to develop and maintain various technical documentation including user manuals, standard operating procedures (SOPs), validation protocols, manufacturing batch records, and training materials. Using advanced technical writing tools and methodologies, you'll ensure documentation meets regulatory requirements while maintaining the highest standards of accuracy and usability.

How Will You Get Here?

Education and Experience
Advanced Degree plus 3 years of experience, or Bachelor's Degree plus 5 years of experience in technical writing, preferably in regulated industries such as pharmaceuticals, biotechnology, or medical devices

Preferred Fields of Study:
Technical Writing, Scientific/Technical Communication, Chemistry, Life Sciences, Engineering or related field

Knowledge,

Skills and Abilities

Demonstrated expertise in GMP/GLP regulations and quality system documentation

Advanced proficiency in content management systems, DITA/XML authoring tools, and Microsoft Office Suite

Strong knowledge of technical documentation best practices and information architecture

Experience with topic-based authoring and single-sourcing methodologies

Excellent project management skills with ability to handle multiple concurrent projects

Superior written and verbal communication skills in English

Strong attention to detail and quality assurance mindset

Proven ability to understand and clearly communicate complex technical/scientific concepts

Experience collaborating with cross-functional teams and managing stakeholder relationships

Proficiency in document control systems and change management processes

Knowledge of HTML, CSS, and digital content development tools

Experience with graphic design tools and video production software preferred

Ability to work independently and as part of teams

Excellent organizational and time management skills

Flexibility to adapt to changing priorities while maintaining deadlines

Compensation
The salary range estimated for this position based in Canada is $68,700.00–$.

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