Scan your resume against ATS criteria for this Senior Consultant - MedTech Regulatory Implementation role at Veeva Systems.
Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our last fiscal year with extensive growth potential ahead
As a https://careers.veeva.com/work-anywhere/ Work Anywhere company, we support your flexibility to work from home or in the office, so you can thrive in your ideal environment.
Join us in https://www.youtube.com/watch?v=TaPSP8cCSKY&ab_channel=Forbes transforming the life sciences industry, committed to making a positive impact on its customers, employees, and communities.
Veeva is looking for an experienced consultant to lead MedTech Regulatory Information Management (RIM) implementations at Veeva’s MedTech customers globally. This role will guide the transformation of our customers’ Regulatory Affairs and Operations processes through industry-leading technology. The MedTech Regulatory consultant will work closely with Professional Services teams to ensure delivery success across the end-to-end regulatory process, covering both data and documentation related workstreams.
for Veeva’s MedTech Regulatory solutions, ensuring successful customer adoption and system configuration
to identify key process steps, gaps, and requirements that impact the implementation approach
, managing complex communication between implementation teams, customer stakeholders, and third parties
and new product features to develop long-term adoption and enhancement roadmaps for Regulatory Operations
and industry best practices, focusing on the continuous improvement of Regulatory data and document management
in Systems Implementation, GxP Systems ownership, or Software Consulting
specifically within the Medical Device or Diagnostics industry
for Veeva RIM or similar solutions (e.g. RegDesk, RIMSYS, IQVIA, Kalypso, Essenvia)
, including FDA, EU MDR/IVDR, Technical Documentation structures and UDI reporting standards
leading IT operations or implementations as a consultant, business analyst, or business sponsor
, with the ability to design creative solutions for complex business requirements
Direct Veeva Vault implementation experience
Experience with Change Management and Management Consulting
Experience with MedTech products or Medical Devices, In-Vitro Diagnostics, Software as a Medical Device (SaMD) or combination products
Experience with UDI (Unique Device Identification) or global submission planning
We value your time and believe in a transparent hiring process. Here is the process you can expect.
Follow the application process and submit your resume.
Within 3 days, you will receive a link to a personality assessment administered by a third party.
Once you complete the assessment, our team will review your full application package and follow up via email with our decision.
If moving to the interview stage, the process is as follows:
A conversation with the hiring manager
A practical case exercise
A final conversation with our group's Senior Leader.
Once all interviews are complete, the manager will be in touch with a final decision.
Medical, dental, vision, and basic life insurance
Flexible PTO and company paid holidays
Retirement programs
1% charitable giving program
Base pay: $80,000 - $200,000
The salary range listed here has been provided to comply with local regulations and represents a potential base salary range for this role. Please note that actual salaries 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. This position may also be eligible for other types of compensation in addition to base salary, such as variable bonus and/or stock bonus.
Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world.
Veeva is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national origin or ancestry, age, disability, marital status, pregnancy, protected veteran status, protected genetic information, political affiliation, or any other characteristics protected by local laws, regulations, or ordinances. If you need assistance or accommodation due to a disability or special need when applying for a role or in our recruitment process, please contact us at mailto:[email protected] [email protected].
, with the ability to design creative solutions for complex business requirements
benefit-corporation-pbc-486e1e9508a6](https://medium.com/@peter.gassner/public-benefit-corporation-pbc-486e1e9508a6) public benefit corporation (PBC), legally bound to balancing the interests of customers, employees, society, and investors.
As a https://careers.veeva.com/work-anywhere/ Work Anywhere company, we support your flexibility to work from home or in the office, so you can thrive in your ideal environment.
Join us in [https://www.youtube.c
How to apply for Senior Consultant - MedTech Regulatory Implementation at Veeva Systems?
Click the "Apply on Company Website" button on this page to submit your application directly on the employer's official portal.
What is the salary for this role?
The salary for this role is $3 per annum.
What experience is required?
8+ years of experience is required.
Is this position still open?
Yes, currently active and accepting applications.
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Senior Consultant - MedTech Regulatory Implementation
Veeva Systems · Massachusetts - Boston
