Technical Writer

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.

The Position

*** 24 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 by a diversified audience. This is essential to ensure we have aligned interpretation and implementation of our Global QMS documents throughout the organization.

Key responsibilities include:

• You will 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.

• You will work with the QMS global authors by breaking down detailed processes into manageable sections, so that they are easy to follow in our QMS global documents.

• You will embed visual workflows to create clear, detailed diagrams that help users understand complex processes and interdependencies.

• You will write complex processes in a concise logical manner for our Global QMS documents.

• You will deliver completed documents to the author to support updates according to the required timelines.

Who You Are:

We are looking for a detail-oriented, 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.

• You have a B.S. in life sciences or equivalent with 5+ years of experience in writing technical documentation.

• Your experience in manufacturing, quality, and knowledge of Health authority regulations is a plus.

• You possess strong collaboration and team-working skills with excellent verbal and written communication in English.

• You are skilled in creating clear, consistent, and structured documents from templates and drafts.

• You are capable of managing multiple projects, meeting tight deadlines, and proficient in Microsoft Word, with a detail-oriented approach.

Who we are

A healthier future drives us to innovate. Together, more than 100,000 employees across the globe are dedicated to advancing science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.

Let’s build a healthier future, together.

Roche Pharma Canada has its office in Mississauga, Ontario and employs over 850 employees. The Mississauga facility is bright, vibrant, fosters collaboration and teamwork, and is reflective of Roche's truly innovative culture.