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HomeCompaniesVeevaSenior Consultant - MedTech QMS Complaints

Senior Consultant - MedTech QMS Complaints

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

Job facts

FieldValue
CompanyVeeva
TitleSenior Consultant - MedTech QMS Complaints
Normalized title-
Department / teamProfessional Services / Quality Cloud Services - NA
LocationMassachusetts - Boston, United States
Work modelRemote / Remote
Employment typeFull Time
Salary$80,000–$200,000 / year
Statusactive
ATS providerLever
Posted / first seen2025-06-23 / 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 Complaints implementations at Veeva’s MedTech customers globally. This role will guide the transformation of our customers’ Complaints Management processes and technology. The MedTech Complaints consultant will work closely with Professional Services teams to ensure delivery success across QMS implementations. #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 Review and analyze existing Customer business process and identify key process steps, gaps, and requirements that would impact implementation approach Lead QMS Complaints implementation workstreams at our customers for Veeva’s MedTech Quality Management solutions Function as a Primary customer liaison managing communication between implementation teams, customer stakeholders, and 3rd parties Analyze customer requirements and new product features to develop customer adoption and enhancement roadmaps 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 Requirements 8+ years of experience in GMP Systems ownership or Software Consulting 5+ years of experience in Complaints Management for Medical Device Strong understanding of FDA, EU MDR/IVDR requirements and Reporting Understanding of relationship between Complaint Handling, CAPA, Nonconformance and Risk Management processes Knowledge of ISO 13485 and 14971, FDA 21CFR Part 803, 820, 822, 806, EU GMP Annex 11 Proven track record leading implementation and/or IT operations as a consultant, business analyst, or IT lead and/or business sponsor Proven ability to work both independently and in teams in a dynamic, fast-moving environment Good understanding of SaaS and GxP principles Ability to quickly understand business requirements and design creative solutions Excellent verbal and written communication skills Experience in the Life Sciences Quality, Manufacturing, or Healthcare spaces Experience with Data or Content Management applications Nice to Have Veeva Vault implementation experience Management Consulting Change Management experience Field Action and Product Return experience Clinical Medical Device, Biologics, and SaMD experience 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 ID24d79b1d11d19032359a41fdfae707ea3f8d565a
Org ID4c200caa-06e8-4cf8-9e9b-bc619d58e153
Source ID6fce17dd-4220-4c57-8376-26c5afb1aaa5
Board ID6fce17dd-4220-4c57-8376-26c5afb1aaa5
Providerlever
Provider Job Key5b662bce-ebd2-4948-84c3-449eb450a8df
TitleSenior Consultant - MedTech QMS Complaints
Normalized Title
Statusactive
Activeyes
Location TextMassachusetts - Boston
DepartmentProfessional Services
TeamQuality Cloud 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/5b662bce-ebd2-4948-84c3-449eb450a8df
Apply URLhttps://jobs.lever.co/veeva/5b662bce-ebd2-4948-84c3-449eb450a8df/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 At2025-06-23 16:54:39Z
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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  "last_changed_at": "2026-05-29T07:00:41.937Z",
  "active_status": "active"
}
Parsed Structured
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    "region": null,
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  "salary_min": 80000,
  "inferred_at": "2026-06-06T07:56:16.741Z",
  "launch_scope": {
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      "region": null,
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Extensions
{}
Native Structured
{
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    {
      "text": "What You'll Do",
      "content": "\n<li>Review and analyze existing Customer business process and identify key process steps, gaps, and requirements that would impact implementation approach</li>\n<li>Lead QMS Complaints implementation workstreams at our customers for Veeva’s MedTech Quality Management solutions</li>\n<li>Function as a Primary customer liaison managing communication between implementation teams, customer stakeholders, and 3rd parties</li>\n<li>Analyze customer requirements and new product features to develop customer adoption and enhancement roadmaps</li>\n<li>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</li>\n"
    },
    {
      "text": "Requirements",
      "content": "\n<li>8+ years of experience in GMP Systems ownership or Software Consulting</li>\n<li>5+ years of experience in Complaints Management for Medical Device</li>\n<li>Strong understanding of FDA, EU MDR/IVDR requirements and Reporting</li>\n<li>Understanding of relationship between Complaint Handling, CAPA, Nonconformance and Risk Management processes</li>\n<li>Knowledge of ISO 13485&nbsp;and 14971, FDA&nbsp;21CFR Part 803, 820, 822, 806, EU GMP Annex 11</li>\n<li>Proven track record leading implementation and/or IT operations as a consultant, business analyst, or IT lead and/or business sponsor</li>\n<li>Proven ability to work both independently and in teams in a dynamic, fast-moving environment</li>\n<li>Good understanding of SaaS and GxP principles</li>\n<li>Ability to quickly understand business requirements and design creative solutions</li>\n<li>Excellent verbal and written communication skills</li>\n<li>Experience in the Life Sciences Quality, Manufacturing, or Healthcare spaces</li>\n<li>Experience with Data or Content Management applications</li>\n"
    },
    {
      "text": "Nice to Have",
      "content": "\n<li>Veeva Vault implementation experience</li>\n<li>Management Consulting</li>\n<li>Change Management experience</li>\n<li>Field Action and Product Return experience</li>\n<li>Clinical Medical Device, Biologics, and SaMD experience</li>\n"
    },
    {
      "text": "Perks & Benefits",
      "content": "\n<li>Medical, dental, vision, and basic life insurance</li>\n<li>Flexible PTO and company paid holidays</li>\n<li>Retirement programs</li>\n<li>1% charitable giving program</li>\n"
    },
    {
      "text": "Compensation",
      "content": "\n<li>Base pay: $80,000 - $200,000</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"
    }
  ],
  "country": "US",
  "createdAt": 1750697679560,
  "updatedAt": null,
  "categories": {
    "team": "Quality Cloud Services - NA",
    "location": "Massachusetts - Boston",
    "commitment": "Full-Time",
    "department": "Professional Services",
    "allLocations": [
      "Massachusetts - Boston"
    ]
  },
  "salaryRange": null,
  "workplaceType": "remote"
}
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