Senior Consultant - Medtech QMS Complaints

in Dublin Ireland. Job Description\n Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. \n At the heart of Veeva are our values: Do the Right Thing, Customer Success, Employee Success, and Speed. \n Join us in transforming the life sciences industry, committed to making a positive impact on its customers, employees, and communities.

The Role\n Veeva is looking for an experienced consultant to lead MedTech Complaints implementations at Veeva’s MedTech customers globally. \n As a member of our Professional Services team, you will be responsible for understanding our customers’ needs, translating

\n The role is a remote, full-time role based in the EU or UK. Qualified candidates must have current legal authorization to work in the EU or UK. Veeva Systems does not anticipate providing sponsorship for employment visa status for this position. What You’ll Do\n \n Review and analyse existing Customer business process and identify key process steps, gaps, and

requirements that would impact implementation approach\n Lead QMS Complaints implementation workstreams at our customers for Veeva’s MedTech Quality Management solutions\n Function as a Primary customer liaison managing communication between implementation teams, customer stakeholders, and 3rd parties\n Analyse customer

requirements and new product features to develop customer adoption and enhancement roadmaps\n Guide customers in adopting Vault and industry best practices as part of post-implementation programs focused on the holistic success and continuous improvement of the customer\n

Requirements\n \n Proven track record leading implementation and/or IT operations as a consultant, business analyst, or IT lead and/or business sponsor\n 5+ years of experience in Complaints Management for Medical Device\n Strong understanding of FDA, EU MDR/IVDR

requirements and Reporting\n Understanding of relationship between Complaint Handling, CAPA, Nonconformance and Risk Management processes\n Knowledge of ISO 13485and 14971, FDA21CFR Part 803, 820, 822, 806, EU GMP Annex 11\n Proven ability to work both independently and in teams in a dynamic, fast-moving environment\n Good understanding of SaaS and GxP principles\n Ability to quickly understand business

requirements and design creative solutions\n Excellent verbal and written communication skills\n Experience in the Life Sciences Quality, Manufacturing, or Healthcare spaces\n Experience with Data or Content Management applications\n Interviewing with Veeva\n We value your time and believe in a transparent hiring process.

\n Compensation\n \n Total compensation: 90,000 - 150,000EUR\n The total compensation range listed here has been provided to comply with local regulations and represents a potential total compensation range for this role. Please note that actual total compensation may vary within the range above or below, depending on experience and location. We look at compensation for each individual and base our offer on your unique

qualifications, experience, and expected contributions. \n As an equal opportunity employer, 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. \n #J-18808-Ljbffr. 000000.