Veeva Developer Job at Robert Half (Blue Bell)

Software developer

Infosmart systems Inc is looking for Software Developers who has experience in d...

Location

United States , Frisco

Salary:

Not provided

InfoSmart Systems

Expiration Date

Until further notice

Requirements

Bachelors degree in computer
experience in designing developing and supporting CRM Siebel, Veeva and salesforce applications

Job Responsibility

Maintain Seibel ePublic sector and case management applications
Develop plans for hardware,system operations and technical procedures
provide inputs for disaster recovery and security plans
Perform trouble shooting, code migration and production support activities and bug fixes

Lead Veeva/Salesforce CRM Developer

The Specialist Software Engineer collaborates with Salesforce/Veeva CRM Admins, ...

Location

United States

Salary:

137457.00 - 171183.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree
OR Master’s degree and 2 years of computer science, IT, or related field
OR Bachelor’s degree and 4 years of computer science, IT, or related field
OR Associate’s degree and 8 years of computer science, IT, or related field
OR High school diploma / GED and 10 years of computer science, IT, or related field
5+ years of experience as a Salesforce CRM Developer
In-depth knowledge of Salesforce development, including experience working with MuleSoft or Databricks integrations
Hands-on experience with the Salesforce security model, including OWD, sharing rules, profiles, and permissions
Experience with Data Loader, data migration tools, and CI/CD tools
Salesforce Developer 2 (required)

Job Responsibility

Leads large CRM migration to ensure configurations, customizations, and data migration are successfully implemented in the new CRM
Drives development in Salesforce/Veeva CRM to build and configure new and existing features
Works closely with Product Owners and cross-functional Development Teams to plan and schedule releases, providing guidance on release dependencies, technical constraints, and risks
Supports the development teams in automating build, test, and deployment processes, enabling continuous integration and continuous delivery in the Salesforce/Veeva ecosystem
Provides ongoing support and troubleshooting for post-release issues, ensuring timely resolution of any problems that arise
Maintains and optimizes existing configurations and customizations by limiting or eliminating technical debt to streamline the system
Partners with Development Teams to ensure agile software delivery and DevOps practices are applied to move most effectively within our CI/CD pipeline
Researches Veeva/Salesforce capabilities as needed to suit business requirements and provides gap analysis
Works closely with other developers in the team, including Product Owners, Business Analysts, Salesforce Admins, QA Analysts, and Scrum Masters, across cross-functional teams
Develops innovative solutions using generative AI technologies

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models, including remote and hybrid work arrangements, where possible

Fulltime

Specialist Software Engineer

Join our team at AMGEN Capability Center Portugal, the #1 company in Best Workpl...

Location

Portugal , Lisbon

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Master’s degree with 5 - 7 years of experience in Computer Science, IT or related
Proficient in programming languages Visual Force, Apex, SQL, Java
Strong expertise in software design principles, and system integration experience with DevOps Tool set (Jira, Git, Jenkins, Copado)
Proven experience (5 years) as Software Engineer, leading the design and development of software solutions
Development experience of Veeva CRM
Proficiency in Salesforce development
Strong understanding of software development methodologies, including Agile and Scrum
Experience with version control systems like Git & Release management tools like Copado
Excellent analytical and solving skills
Strong verbal and written communication skills

Job Responsibility

Deliver complex software projects end-to-end—from ideation through deployment—ensuring alignment with business objectives and technology strategy
Manage delivery scope, risks, and timelines in coordination with the Software Engineering team, ensuring completion within Agile frameworks
Contribute to both front-end and back-end development using Veeva CRM/Salesforce
Rapidly prototype solutions to translate business concepts into functional code for quick validation and iterative improvements
Provide hands-on technical expertise and contribute to high-quality engineering outcomes
Provide technical mentorship across the engineering team
Influence the technical roadmap and lead cross-team initiatives
Conduct code reviews to ensure code quality and adherence to best practices, including performance metrics, code quality, and coverage
Maintain high standards of code quality, enforce coding practices, and ensure comprehensive test coverage
Create and maintain documentation on software architecture, design, deployment, disaster recovery, and operations

What we offer

Work That Matters– Build tech that accelerates scientific breakthroughs and helps patients worldwide
Modern Tech Stack– Cloud-first, automation-focused, AI-powered
Global Scale, Agile Mindset– Collaborate across continents while working in nimble, high-impact teams
Continuous Learning– Access to certifications,trainings, mentorship, and career mobility
AMGEN Total Rewards Plan– Comprehensive benefits in healthcare, finance, and well-being
Flexibility– Hybrid work model with time split between our Lisbon office and remote work

Fulltime

Associate IS Engineer - Veeva Vault Promomats_Medcomms

In this vital role in the Veeva Vault team you will be responsible for designing...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Bachelor’s degree and 2 to 6 years of Information Systems experience or related field
Experience with Amgen’s Vault PromoMats and Vault MedComm, including Veeva configuration settings and custom builds
Strong knowledge of information systems and network technologies
Experience in building configured and custom solutions on Veeva Vault Platform
Experience in managing systems, implementing and validating projects in GxP regulated environments
Extensive expertise in SDLC, including requirements, design, testing, data analysis, creating and managing change controls
Proficiency in programming languages such as Python, JavaScript etc.
Solid understanding of software development methodologies, including Agile and Scrum
Experience with version control systems such as Git
Veeva Vault Platform Administrator or Equivalent Vault Certification (Must-Have)

Job Responsibility

Designing, developing, and maintaining software applications and solutions in Amgen’s Vault PromoMats and Vault MedComm
Ensuring the availability and performance of critical systems and applications
Working closely with product managers, designers, and other engineers to create high-quality, scalable software solutions
Automating operations, monitoring system health, and responding to incidents to minimize downtime
Possesses strong rapid prototyping skills and can quickly translate concepts into working code
Lead day to day operations and maintenance of Amgen’s Amgen’s Vault PromoMats and Vault MedComm and its hosted applications
Stay updated with the latest trends, advancements and standard processes for Veeva Vault Platform ecosystem
Design, develop, and implement applications and modules, including custom reports, SDKs, interfaces, and enhancements
Analyze and understand the functional & technical requirements of applications, solutions and systems, translate them into software architecture and design specifications
Develop and complete unit tests, integration tests, and other testing strategies to ensure the quality of the software following IS change control and GxP Validation process while exhibiting expertise in Risk Based Validation methodology

What we offer

Competitive and comprehensive Total Rewards Plans that are aligned with local industry standards

Fulltime

New

Veeva Clinical Business Administration Specialist

Empower clinical teams by optimizing the Veeva Vault systems that keep trials ru...

Location

United States , Boston

Salary:

Not provided

Proclinical

Expiration Date

Until further notice

Requirements

Strong oral and written communication skills
excellent organizational abilities and attention to detail
ability to work both independently and collaboratively in a fast-paced environment
familiarity with clinical trial processes, ICH-GCP guidelines, and essential documents
critical thinking and problem-solving skills
proficiency in Microsoft Office applications
knowledge of GXP systems in the pharmaceutical or CRO industry, particularly CTMS or related systems
understanding of computer system validation and system lifecycles
experience with Veeva Vault Clinical eTMF and CTMS systems
database management and reporting experience

Job Responsibility

Develop and maintain Veeva Vault reports and dashboards, ensuring clear documentation for user understanding
collaborate with the Change Management team to draft system training materials, including quick reference guides and presentations
provide end-to-end user support, including troubleshooting, technical assistance, and analysis of request trends
manage business process-driven values, metadata, controlled vocabularies, and picklists
liaise with internal and external IT teams to address bugs, discuss functionality, and implement best practices
identify opportunities for process improvements and system enhancements, including performing system health checks and gathering user feedback
support PQ execution and participate in training sessions, office hours, and knowledge-sharing events
manage CTMS requests, such as study record creation, team roster updates, and troubleshooting
communicate new release information to users in an accessible and efficient manner
oversee TMF requests, including monitoring document integration metrics, conducting post-migration quality checks, and reviewing audit trails

New

District Manager Alps

The District Manager ALPS is responsible for developing and implementing the sal...

Location

Austria , Vienna

Salary:

Not provided

Norgine

Expiration Date

Until further notice

Requirements

Educated to degree level, preferably in a life sciences subject
At least 5 years of experience in the pharmaceutical industry in Switzerland and/or Austria of which three 3 years in a sales management positions
Excellent communication and presentation skills, both verbal and written in German and English
Proven ability to lead, manage and coach the staff to exceed targets and to drive the business
Willingness to travel
Knowledge of the market access environment
Capable of managing complex situations
Strong communication and influencing skills
Ability to work effectively as part of a successful and highly motivated Management team
Excellent leadership and managerial Skills

Job Responsibility

Responsible for delivering the assigned national sales objectives
Grow the sales of assigned products in Norgine Alps according to agreed sales targets
Develop & implement national sales strategies for all product portfolio & launch products for Austria and Switzerland
Participate in the development and implementation of the Alps total product portfolio
Analyze sales channels, major account dynamics, the markets and the potential of our products as well as the competitors
Define customer segmentation per brand
Implement call plans by target with sales team
Develop, implement & track Key Account plans per brand with sales team
Contribution to marketing strategies per brand
Contribution to development of promotional material through the CORE Brand Teams

New

Sr. Associate IS Engineer

The IS Engineeris responsible for designing, developing, and maintaining softwar...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Master’s degree and 3 to 7 years of Computer Science, IT or related field experience
Bachelor’s degree and 5 to 9 years of Computer Science, IT or related field experience
Diploma and 7 to 9 years of Computer Science, IT or related field experience
Hands on experience with Veeva Vault configuration
Proficiency in programming languages such as Python, JavaScript preferred or other programming languages
Strong understanding of software development methodologies, including Agile and Scrum
Solid understanding & Proficient in writing SQL queries

Job Responsibility

Possesses strong rapid prototyping skills and can quickly translate concepts into working code
Lead day to day operations and maintenance of Veeva Clinical Operations vault applications
Stay updated with the latest trends, advancements and standard process for Veeva Clinical Operations Vault applications
Design, develop, and implement applications and modules, including custom reports, interfaces, and enhancements
Analyze and understand the functional and technical requirements of Veeva Clinical Operations Vault applications, solutions and systems and translate them into software architecture and design specifications
Develop and execute unit tests, integration tests, and other testing strategies to ensure the quality of the software following IS change control and GxP Validation process
Work closely with cross-functional teams, including product management, design, and QA, to deliver high-quality software on time
Maintain detailed documentation of software designs, code, and development processes
Work on integrating with other systems and platforms to ensure seamless data flow and functionality
Stay up to date on Veeva Vault Features, new releases and best practices

Global Regulatory Affairs Lead, Wellbeing Collective

Lead global regulatory strategy for a fast-growing health supplement business (W...

Location

United States , Hoboken

Salary:

227700.00 - 569250.00 USD / Year

Unilever

Expiration Date

Until further notice

Requirements

Bachelor's Degree in Science (e.g., Pharmacy/Pharm D, Biology, Chemistry) or a higher degree (Ph.D.)
A specialized degree in Regulatory Affairs is highly desirable
Minimum 10+ years of progressive experience in Regulatory Affairs within the Consumer Healthcare or Nutraceutical industry
Demonstrated success in developing and executing regulatory strategies for health products across multiple global regions and different product categories
Proven experience in a global lead regulatory role with a comprehensive understanding of regional regulatory requirements and dynamics across multiple regions (U.S., EU, and/or other international markets)
Strong knowledge of global regulatory requirements and submission formats
Proven experience managing complex regulatory deliverables across product lifecycle stages
Significant experience in interactions with FDA, EMA, and other global regulatory agencies
Deep understanding of the product development process for ingestible health products
Strong sense of urgency and ability to react decisively to regulatory alerts, product challenges, and sustainability trends

Job Responsibility

Build a unified, scalable regulatory capability across a diverse portfolio of acquired businesses and international organization
Develop and Champion Strategy: Define and execute the comprehensive, long-term regulatory strategy for Wellbeing portfolio globally, ensuring alignment with commercial goals
Drive Innovation Pipeline: Serve as the regulatory lead in the global innovation process, providing scientific and regulatory input for new product development, and market entry, including claims support
Opportunity Identification: Proactively monitor regulatory trends and intelligence to identify new product opportunities and potential risks, presenting actionable recommendations to the Wellbeing Collective Operating Companies and International Teams
Set Standards: Set standards and decision-making frameworks for global compliant labeling, claims, and marketing communications. Develop SOPs, define performance metrics, and guide teams on regulatory best practices
International Expansion: Direct and manage regulatory procedures worldwide, including dossier preparation, label development and claims support, and global marketing applications. Provide oversight for preparation and delivery of materials for regulatory agency meetings and inspections
Provides a vision and leadership for Policy and Regulation to assure that appropriate Wellbeing representation in external advocacy activities and industry forums is achieved
Participates in due diligence and provides regulatory advice and perspective on all potential licensing and M&A deals
Brand Portfolio Accountability: Act as the regulatory portfolio owner, ensuring timely and compliant maintenance of the Wellbeing Portfolio
Risk Management: Proactively identify and communicate potential regulatory risks, offering clear mitigation options

What we offer

health insurance (including prescription drug, dental, and vision coverage)
retirement savings benefits
life insurance and disability benefits
parental leave
sick leave
paid vacation and holidays
access to numerous voluntary benefits
bonus eligible
Long-Term Incentive (LTI) eligible

Fulltime

Veeva Developer

Robert Half

Location:
United States , Blue Bell

Category:
IT - Software Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
January 25, 2026

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