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.
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 Quality Management Systems (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.
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
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 to 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 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.
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.
** Relocation benefits not available for this position"
The expected salary range for this position based on the primary location of Mississauga is 89,256.00 and 117,148.50 of hiring range. Actual pay will be determined based on experience, qualifications, and other job-related factors as determined by the company.We use artificial intelligence to screen, assess or select applicants for this role.
This posting is for an existing vacancy at Hoffmann-La Roche Ltd.
A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance 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 is an Equal Opportunity Employer.