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HomeCompaniesVeevaSenior Consultant - MedTech Regulatory Implementation

Senior Consultant - MedTech Regulatory Implementation

Veeva · Massachusetts - Boston · Remote · Active · $80,000–$200,000 / year · Lever

Job facts

FieldValue
CompanyVeeva
TitleSenior Consultant - MedTech Regulatory Implementation
Normalized title-
Department / teamProfessional Services / DevCloud Services - NA
LocationMassachusetts - Boston, United States
Work modelRemote / Remote
Employment typeFull Time
Salary$80,000–$200,000 / year
Statusactive
ATS providerLever
Posted / first seen2026-04-29 / 2026-05-29
Changed / last seen2026-05-29 / 2026-06-06

Related slices

PageWhat it containsOpen
Company jobsActive postings from Veeva.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through Lever.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Massachusetts - Boston.Open
Department jobsActive postings in Professional Services.Open
Work model jobsActive Remote postings.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanyVeeva
Source6fce17dd-4220-4c57-8376-26c5afb1aaa5
ATS providerLever

Description

Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our last fiscal year with extensive growth potential ahead. At the heart of Veeva are our values: Do the Right Thing, Customer Success, Employee Success, and Speed. We're not just any public company – we made history in 2021 by becoming a public benefit corporation (PBC), legally bound to balancing the interests of customers, employees, society, and investors. As a 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 transforming the life sciences industry, committed to making a positive impact on its customers, employees, and communities. The Role 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. #LI-RemoteUS #LI-MidSenior 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 [email protected]. What You'll Do Lead RIM implementation workstreams for Veeva’s MedTech Regulatory solutions, ensuring successful customer adoption and system configuration Review and analyze existing customer business processes to identify key process steps, gaps, and requirements that impact the implementation approach Function as a primary customer liaison , managing complex communication between implementation teams, customer stakeholders, and third parties Analyze customer requirements and new product features to develop long-term adoption and enhancement roadmaps for Regulatory Operations Guide customers in adopting Veeva RIM and industry best practices, focusing on the continuous improvement of Regulatory data and document management Requirements 8+ years of experience in Systems Implementation, GxP Systems ownership, or Software Consulting 4+ years of experience working with or in Regulatory Operations or Regulatory Affairs specifically within the Medical Device or Diagnostics industry Direct experience with software implementation for Veeva RIM or similar solutions (e.g. RegDesk, RIMSYS, IQVIA, Kalypso, Essenvia) Strong understanding of global regulatory requirements , including FDA, EU MDR/IVDR, Technical Documentation structures and UDI reporting standards Proven track record leading IT operations or implementations as a consultant, business analyst, or business sponsor Excellent verbal and written communication skills , with the ability to design creative solutions for complex business requirements Nice to Have 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 Perks & Benefits Medical, dental, vision, and basic life insurance Flexible PTO and company paid holidays Retirement programs 1% charitable giving program Compensation 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.

Full job record

Job ID263c83a9e9df8ee7ab704d4909adc45f1c0dc2a4
Org ID4c200caa-06e8-4cf8-9e9b-bc619d58e153
Source ID6fce17dd-4220-4c57-8376-26c5afb1aaa5
Board ID6fce17dd-4220-4c57-8376-26c5afb1aaa5
Providerlever
Provider Job Key2f4c7e27-ab68-46d6-ae3f-fa8f79c7888c
TitleSenior Consultant - MedTech Regulatory Implementation
Normalized Title
Statusactive
Activeyes
Location TextMassachusetts - Boston
DepartmentProfessional Services
TeamDevCloud Services - NA
Employment TypeFull-Time
Workplace Typeremote
Remote Policyremote
CountryUnited States
Region
CityMassachusetts - Boston
Salary RawBase pay: $ 80,000 - $200,000 The salary range listed here has been provided to comply with local regulations
Salary Min80,000
Salary Max200,000
Salary CurrencyUSD
Salary Periodyear
Source URLhttps://jobs.lever.co/veeva/2f4c7e27-ab68-46d6-ae3f-fa8f79c7888c
Apply URLhttps://jobs.lever.co/veeva/2f4c7e27-ab68-46d6-ae3f-fa8f79c7888c/apply
First Seen At2026-05-29 07:00:41Z
Last Seen At2026-06-06 07:56:17Z
Last Checked At2026-06-06 07:56:17Z
Last Changed At2026-05-29 07:00:41Z
Inactive At
Source Posted At2026-04-29 21:58:03Z
Source Updated At
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=lever/board=veeva/date=2026-06-06/2026-06-06T07-56-12-755Z-d8b56e04cea2017ece19014d0050a0f7ca5f16a9d4b07b8535238de2cbeeb64d.json
Event Fields
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  "active_status": "active"
}
Parsed Structured
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Extensions
{}
Native Structured
{
  "lists": [
    {
      "text": "What You'll Do",
      "content": "<div>\n\n<li><strong>Lead RIM implementation workstreams</strong> for Veeva’s MedTech Regulatory solutions, ensuring successful customer adoption and system configuration</li>\n<li><strong>Review and analyze existing customer business processes</strong> to identify key process steps, gaps, and requirements that impact the implementation approach</li>\n<li><strong>Function as a primary customer liaison</strong>, managing complex communication between implementation teams, customer stakeholders, and third parties</li>\n<li><strong>Analyze customer requirements</strong> and new product features to develop long-term adoption and enhancement roadmaps for Regulatory Operations</li>\n<li><strong>Guide customers in adopting Veeva RIM</strong> and industry best practices, focusing on the continuous improvement of Regulatory data and document management</li>\n\n</div>"
    },
    {
      "text": "Requirements",
      "content": "<div>\n\n<li><strong>8+ years of experience</strong> in Systems Implementation, GxP Systems ownership, or Software Consulting</li>\n<li><strong>4+ years of experience working with or in Regulatory Operations or Regulatory Affairs</strong> specifically within the Medical Device or Diagnostics industry</li>\n<li><strong>Direct experience with software implementation</strong> for Veeva RIM or similar solutions (e.g. RegDesk, RIMSYS, IQVIA, Kalypso, Essenvia)</li>\n<li><strong>Strong understanding of global regulatory requirements</strong>, including FDA, EU MDR/IVDR, Technical Documentation structures and UDI reporting standards</li>\n<li><strong>Proven track record</strong> leading IT operations or implementations as a consultant, business analyst, or business sponsor</li>\n<li><strong>Excellent verbal and written communication skills</strong>, with the ability to design creative solutions for complex business requirements</li>\n\n</div>"
    },
    {
      "text": "Nice to Have",
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    },
    {
      "text": "Perks & Benefits",
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    },
    {
      "text": "Compensation",
      "content": "<div>\n\n<li>Base pay: $<span data-sheets-root=\"1\">80,000 - $200,000</span></li>\n<li>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.</li>\n\n</div>"
    }
  ],
  "country": "US",
  "createdAt": 1777499883062,
  "updatedAt": null,
  "categories": {
    "team": "DevCloud Services - NA",
    "location": "Massachusetts - Boston",
    "commitment": "Full-Time",
    "department": "Professional Services",
    "allLocations": [
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  "salaryRange": null,
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}
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