Global Clinical Master Data Specialist

Roche•Mississauga, ON

4d•CA$89,256 - CA$117,149•Onsite

About The Position

At Roche, we foster a culture where individuality is embraced, and personal expression, open dialogue, and genuine connections are encouraged. We value, accept, and respect everyone for who they are, enabling them to thrive personally and professionally. Our mission is to prevent, stop, and cure diseases and ensure universal access to healthcare for present and future generations. Join Roche, where every voice matters. The mission of the Global Clinical Supply Chain Organisation (PTDS) is to ensure that no patient is left without treatment and no clinical trial is delayed. Our vision is to provide innovative and sustainable clinical supply solutions to anyone, anywhere, at any time. By joining our team, you will play a key role in advancing Roche’s diverse and robust biopharmaceuticals pipeline, encompassing over 100 molecules in approximately 500 clinical trials across seven disease areas in more than 80 countries.

Requirements

University degree in Life Sciences, Computer Science, Business Administration, or a closely related field.
Minimum of 5 years of professional experience in Master Data Management.
Strong preference for background knowledge in Clinical Supply within the pharmaceutical industry.
Deep, foundational understanding of GMP and GCP guidelines.
Highly skilled in navigating and maintaining complex enterprise systems, specifically expert-level knowledge of SAP R3P Clinical, S/4HANA, MDGM, APO, and OMP.
Proficient with VEEVA platforms, possessing the ability to effectively handle Deviations, Planned Events, and CAPA Records alongside conducting robust root-cause analyses.
High cultural awareness coupled with excellent communication skills.
Ability to thrive independently or collaboratively while staying calm and proactive under pressure.
Fluent in written and spoken English.

Nice To Haves

Professional proficiency in German as a significant asset to our global workflows.

Responsibilities

Manage GMP/Quality-relevant master data lifecycle processes, creating and updating Material Masters, Classifications, and business partner/vendor data.
Oversee production-related data architectures, including the precise maintenance of Master Recipes, Bills of Materials (BOM), and Production Versions.
Ensure flawless data alignment across SAP R3P Clinical, S/4HANA, APO, and OMP landscapes to fully support global distribution and production planning.
Lead Engineering Change Management (ECM) workflows and coordinate Engineering Change Requests (ECR) alongside MDGM workflows with global requestors.
Partner closely with Production, Supply Chain, Quality, and Pharma Affiliates to successfully translate operational needs into accurate system configurations.
Act as the single point of contact for master data troubleshooting, while managing system user accounts and roles via the Corporate Identity Management (CIDM) platform.
Oversee Quality Records within VEEVA (Deviations, CAPAs), update SOPs/SPTs, and monitor Key Performance Indicators (KPIs) to lead process optimization initiatives.