Senior Implementation Consultant RIMS – MedTech Services in Paris

Job Description

Join American cloud-computing and Software company Veeva Systems, currently hiring Senior Implementation Consultant RIMS – MedTech Services in Paris , Apply Veeva careers in Paris .


Position : Senior Implementation Consultant RIMS – MedTech Services

Location : Paris,

Job Category : Professional Services


Job Details

Veeva is a mission-driven organization that aspires to help our customers in Life Sciences and Regulated industries bring their products to market, faster. We are shaped by our values: Do the Right Thing, Customer Success, Employee Success, and Speed. Our teams develop transformative cloud software, services, consulting, and data to make our customers more efficient and effective in everything they do. Veeva is a work anywhere company. You can work at home, at a customer site, or in an office on any given day. As a Public Benefit Corporation, you will also work for a company focused on making a positive impact on its customers, employees, and communities.
The Role
Do you love solving business problems with technology? Do you thrive on learning and navigating new situations? Come help us transform how regulatory information is managed in MedTech companies! Veeva’s Vault RIM suite is the industry’s only unified software solution that provides fully integrated regulatory information management (RIM) capabilities including data and document management, submission publishing, and archival on a single cloud-based platform, adapted for Medical Devices and Diagnostics companies.   Veeva is looking for consultants with implementation experience and a passion for helping customers optimize their regulatory data and document management process. 
As a key member of the Professional Services organization, the Consultant will be responsible for understanding our customers’ global regulatory needs, translating requirements into solution design, and defining global strategies for deploying our cloud-based solution for managing regulatory information across the enterprise.   The Consultant will also work collaboratively across Veeva, contributing ideas, enhancing our delivery model, and working closely with our product management team to meet the evolving needs of the MedTech industry.   This is a remote, full-time permanent role with Veeva. There is no work location requirement. This is a customer-facing role with the requirement to travel up to 40%. Opportunities are available across Europe. Qualified EU-based candidates are encouraged to apply. What You’ll Do Lead implementations of Vault RIM suite for MedTech (including Vault Registrations, Vault Submissions, Vault Submissions Publishing, and Vault Submissions Archive). Conduct requirements workshops, designs, and configuration review iterations with our customers’ Regulatory and IT stakeholders. Ensure adherence to industry best practices. Look after customers’ success from the beginning to the end of the engagement. Mentor project team members and junior consultants Provide insight and recommendations to improve our technology and work closely with our Product team to ensure the best solution for our customers. Requirements 8 + years of relevant work experience in Services Delivery or Consulting. Deep Knowledge of product development and regulatory submissions processes in MedTech. Implementation experience either as a consultant, business, or IT representative for at least one of the following: Document Management systems (Documentum, OpenText, SharePoint), Registration Data Tracking systems, UDI tracking systems, eCTD or Submission Publishing systems Proven ability to manage diverse customers and /or stakeholders and ability to communicate at multiple levels of an organization Self-starter and motivated individual with the proven ability to work independently in a dynamic environment.  4-year degree or equivalent work experience required  Ability to travel up to 40% Nice to Have Computer Science, Life Science, or related degree preferred Regulatory Affairs, Regulatory Operations, or Post Market Surveillance experience in the Medical Devices or Diagnostics space  Familiarity with MedTech Quality Systems regulatory requirements and guidelines: ISO 13485, 2017/745, 2017/746, 21 CFR Part 11, GAMP Experience in Services Delivery Management and Pre-Sales presentations with SaaS/Cloud Perks & Benefits Allocations for continuous learning & development  Health & wellness programs #RemoteFrance Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world. Veeva is committed to fostering a culture of inclusion and growing a diverse workforce. Diversity makes us stronger. It comes in many forms. Gender, race, ethnicity, religion, politics, sexual orientation, age, disability and life experience shape us all into unique individuals. We value people for the individuals they are and the contributions they can bring to our teams.


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