Senior Quality Consultant – MedTech Services in Frankfurt

Job Description

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


Position : Senior Quality Consultant – MedTech Services

Location : Frankfurt,

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
Are you driven and self-motivated?  Are you passionate about bringing purpose-built technologies that enable greater compliance and process efficiencies to MedTech Companies? Are you looking for a collaborative work environment where you are encouraged to contribute and share your thoughts and ideas?   Veeva is looking for experienced professionals to implement Veeva Vault Quality solutions for our Medical Device and Diagnostic customers. The ideal candidate will utilize their industry experience to transform the way our customers collect, maintain, and Quality related processes and documentation. They will also contribute ideas and work with other Veeva team members to innovate and refine our internal processes, share feedback and work with our product team, and enhance our delivery model to meet the ever-changing 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 Veeva Vault Quality implementations and handle project management responsibilities such as resource planning, project risk management, leading cross-functional teams, and budget tracking & forecasting of the engagement. Conduct Vault Design Review and Configuration workshops with MedTech stakeholders from Business and IT: gather requirements, design & prototype, configure and support the validation of the delivered Quality processes Work closely with customers’ business and IT stakeholders and develop scalable solutions that meet Quality regulatory compliance and customer requirements. Mentor project team members and junior consultants Continue to develop industry knowledge and enhancements the delivery model to meet the changing business needs of Veeva and our customers. Provide insight and recommendations to improve our technology and work closely with our Product team to ensure the best solutions for our customers.  Requirements 8 + years of relevant work experience within Life Sciences, Healthcare, or other regulated industries (ex. Consumer Goods, Chemical, Cosmetics) Experience implementing, designing solutions, and supporting software applications.   Self-starter and motivated individual with the proven ability to work independently in a dynamic environment.  Intermediate knowledge of Quality related processes (e.g. CAPA, Complaints, Non-Conformance, Product Surveillance, Change Management) Understanding of compliance and computer systems validation requirements.  Proven ability to manage diverse customers and /or stakeholders and ability to communicate at multiple levels of the organization Ability to quickly understand customer requirements and create corresponding solution designs Knowledge of SaaS/Cloud software solutions Bachelor’s degree or equivalent work experience required Nice to Have Work experience in Medical Devices and/or Diagnostics space Computer Science, Life Science, or related degree preferred.  Strong knowledge of MedTech industry standards and regulatory requirements (e.g.: FDA QSR, ISO 13485, 21 CFR Part 11, 21 CFR 820, 210, GAMP) Direct experience with regulated systems or data-driven applications such as Veeva Vault solutions, NextDocs, Documentum, FirstDoc /FirstPoint, Trackwise, Medidata, Liquent Insight Experience with PLM and LIMs systems such as Arena, TeamCenter, Propel, Agilent, Labworks SaaS/Cloud delivery experience  Experience in Services Delivery Management or Pre-Sales presentations and demonstrations. Perks & Benefits Allocations for continuous learning & development  Health & wellness programs #RemoteGermany 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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