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You will be updated with latest job alerts via emailAt 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.
About Roche Informatics
In Roche Informatics we build on Roches 125year history as one of the worlds largest biotech companies globally recognized for providing transformative innovative solutions across major disease areas. We combine human capabilities with cuttingedge technological innovations to do now what our patients need next. Our commitment to our patients needs motivates us to deliver technology that evolves the practice of medicine.
Be part of our inclusive team at Roche Informatics where were driven by a shared passion for technological novelties and optimal IT solutions.
You are looking for a company where you have the opportunity to pursue your interests across functions and geographies.
About the position
As an Enterprise Technology Expertise Engineer you will join the Enterprise Engineering cluster in the Product Development Integration and Engineering chapter you will partner with other internal experts specializing in various aspects of Enterprise engineering. Together the team collaborates on multiple products that contribute to Roches internal business requirements.
As a Technology Expertise Engineer you will be accountable for technical leading developing optimizing and managing IT services/applications in Veeva with focus on Clinical Trial Management Regulatory Information Management Quality Management and Quality Documents. You will also focus on ensuring costeffectiveness scalability and security in all aspects of the digital product lifecycle including maintenance activities. As part of enterprise engineering you will be involved in understanding the business application processes and functions.
Your key responsibilities :
Lead collaborate and facilitate crossfunctional experts to deliver a particular solution with a good understanding of the business requirements.
Take leadership coordinate and act as a subject matter expert for Veeva Vaults Clinical Regulatory Quality Management and Quality Documents to support the design implementation and maintenance of reliable and performant solutions.
Ensuring costeffectiveness scalability and security in all aspects of the digital product lifecycle
Responsible for the quality of the technical deliverables which also includes peer reviews
Develop and publish the application/prototype with the knowledge of using DevOps according to the underlying infrastructure.
Lead the implementation and maintenance of efficient Continuous Integration / Continuous Delivery pipelines to automate the delivery process.
Your qualifications and experience:
Deep Knowledge and Proficiency in Veevas architecture data models configuration tools and integration methods.
Technical functional knowledge with Veeva applications specifically those on the Vault Platform like Clinical RIM QMS QualityDocs. Any other additional Veeva skills are also an asset.
Experience with Veeva Connections/Connectors and User Provisioning Service implementation
Certification of the Veeva platform will be valueadded.
Clinical Regulatory and Quality Management Domain Knowledge: Understanding of clinical/regulatory/quality processes regulatory requirements and standards like Good Clinical Practice (GCP).
Well rounded technical capability in transactional systems integrations reporting data warehousing and security
Strong Project Management and Coordination skills.
Possess a combination of leadership analysis handson problem solving and a customerservice mindset.
Essential effective oral and written communication skills in English.
Working knowledge of Computer Systems Validation (CSV) and GxP.
Working knowledge of regulations like HIPAA and GDPR in the healthcare industry
Moderate travel is required and the ability to work across multiple time zones.
Education / Years of Experience:
8 Years of relevant work experience with Bachelors degree in Computer Science/IT/Engineering or 8 Years of relevant work experience
At least 5 years experience of working in one or more multinational work environments (pharma/life science industry experience is a plus).
Excellent analytical thinking and problemsolving skills
Excellent communication and collaboration skills
Good understanding of regulatory compliance and security
Experience with other cloud systems (AWS Azure GCP) is beneficial.
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 lifechanging healthcare solutions that make a global impact.
Lets build a healthier future together.
Roche is an Equal Opportunity Employer.
Full-Time