Technical Writer

** 18 month contract position**

A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche.

At Roche, we thrive to deliver more benefits to our patients as part of our 10-year Pharma vision. The QMS Governance Chapter provides a future-forward Quality Management framework of requirements, processes, tools, and documented content for Roche PT employees to execute consistently and compliantly, which ultimately assures the end product is of high quality for our patients.

The Opportunity:

As a QMS Technical writer, you will partner with our Global QMS authors to ensure information is written clearly and can be followed and understood to a diversified audience. This is essential to ensure we have aligned interpretation and implementation of our Global QMS documents throughout the organization

• Translate complex information into lean, easily digestible pieces of written content.
• Simplify technical jargon, as appropriate, and intricate concepts, ensuring the information is clear and understood by a broad audience.
• Work with the QMS Process Owners/Authors by breaking down detailed processes into manageable sections, so that they are easy to follow in our QMS global documents
• Embed visual workflows to create clear, detailed diagrams that help users understand complex processes and interdependencies
• Write complex processes in a concise, logical manner for our Global QMS documents.
• Deliver completed documents to the author to support updates according to the required timelines

Who You Are:

We are looking for a detail orientated, collaborative team member who can work effectively with a diverse group of authors. You bring experience in technical writing procedures and policies that serve a large network of users.

• B.S. in life sciences or equivalent.
• 5+ years of proven experience in writing technical documentation
• Manufacturing and/or Quality experience in the pharmaceutical or related industry and knowledge of Health authority regulations would be an asset.
• Effective collaboration and team-working skills
• Excellence verbal and written communication skills in English are a must
• Skilled in drafting documentation from provided templates and drafts to efficiently produce clear, consistent, and structured documents.
• Ability to translate complex technical information into easily digestible content
• Ability to undertake multiple projects and deliver on tight deadlines
• Proficient in Microsoft Word
• Detail-oriented

**This position is not eligible for relocation**