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.
** 18 month contract position**
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**
The expected salary range for this position based on the primary location of Mississauga is 89256.00 and 117148.50 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 100000 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.
Lets build a healthier future together.
Roche is an Equal Opportunity Employer.
QMS Technical Writer • Mississauga, Ontario, Canada
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