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Veeva Consulting Jobs in Indiana (NOW HIRING)

Zifo

Veeva QMS Consultant

Bloomington, IN · On-site +1

Zifo is seeking a highly skilled and detail-oriented Veeva QMS consultant to support the implementation, optimization, and ongoing management of Quality Management Systems (QMS) within a regulated ...

Zifo

Veeva QMS Consultant

Bloomington, IN · On-site +1

Zifo is seeking a highly skilled and detail-oriented Veeva QMS consultant to support the implementation, optimization, and ongoing management of Quality Management Systems (QMS) within a regulated ...

Accenture

Adobe AEM Functional Consultant

Carmel, IN · On-site

$70.35K - $196K/yr

A marketing technology consultant with a passion for digital transformation in the Life Sciences ... Familiarity with Medical, Legal, Regulatory (MLR) review processes and tools like Veeva Vault Bonus ...

Jj

Sr. Manager, Quality & Regulatory

Warsaw, IN · On-site +1

... consultation with works councils and other employee representative bodies, as may berequired ... name for Veeva. * Compliance/admin: Upload/submitfilings; print and hand-deliver to agencies ...

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Veeva Consulting information

What are the key skills and qualifications needed to thrive as a Veeva Consultant, and why are they important?

To thrive as a Veeva Consultant, you need expertise in life sciences processes, deep familiarity with Veeva Vault or CRM platforms, and a relevant degree in fields such as life sciences, IT, or business. Hands-on experience with Veeva applications, certifications like Veeva Vault Admin, and knowledge of related systems such as Salesforce are highly valuable. Strong analytical thinking, clear communication, and the ability to manage client relationships set top consultants apart. These skills and qualifications ensure effective implementation, user adoption, and optimal client outcomes in compliance-driven environments.

How does a Veeva Consultant typically collaborate with clients and internal teams during an implementation project?

As a Veeva Consultant, collaboration is a key part of the role. Consultants work closely with client stakeholders to gather business requirements, configure Veeva solutions, and ensure successful adoption. They often facilitate workshops, provide training, and serve as a bridge between technical teams and business users. Internally, Veeva Consultants coordinate with project managers, developers, and quality assurance teams to deliver projects on time and meet client expectations. Effective communication and adaptability are essential to address challenges and drive project success.

What is Veeva Consulting?

Veeva Consulting refers to professional services provided by experts who specialize in implementing, customizing, and optimizing Veeva Systems software for life sciences companies. Veeva Systems offers cloud-based solutions for managing clinical trials, regulatory documents, quality processes, and customer relationships within the pharmaceutical and biotech industries. Veeva consultants help organizations streamline workflows, ensure regulatory compliance, and maximize the value of their Veeva applications. They often work on projects like system integrations, migration, training, and support.

What is the difference between Veeva Consulting vs Veeva Developer?

AspectVeeva ConsultingVeeva Developer
Required CredentialsVeeva certifications, industry knowledgeVeeva certifications, technical skills
Work EnvironmentClient-facing, project managementDevelopment, coding, system customization
Employer & Industry UsageConsulting firms, pharma, biotechPharma companies, tech teams
Common Search & ComparisonFocus on strategic implementationFocus on system development & coding

Veeva Consulting professionals primarily focus on strategic implementation, project management, and client interactions within the pharmaceutical and biotech industries. In contrast, Veeva Developers concentrate on coding, system customization, and technical development within Veeva platforms. Both roles require Veeva certifications but serve different functions in the Veeva ecosystem.

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What cities in Indiana are hiring for Veeva Consulting jobs? Cities in Indiana with the most Veeva Consulting job openings:
Veeva Consulting jobs near you

Veeva QMS Consultant

Zifo

Bloomington, IN • On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 29 days ago

Job description

**This role is open to remote candidates who have availability to travel to the client in Bloomington, IN on a regular basis**
Zifo is seeking a highly skilled and detail-oriented Veeva QMS consultant to support the implementation, optimization, and ongoing management of Quality Management Systems (QMS) within a regulated scientific environment. This role will focus on leveraging Veeva Vault QMS solutions to ensure compliance, streamline processes, and enhance operational efficiency across quality and regulatory functions.
The ideal candidate combines strong scientific domain knowledge with technical expertise in QMS platforms and Veeva Vault applications.
Responsibilities:
  • Lead the implementation, configuration, and support of QMS applications, with a focus on Veeva Vault QMS.
  • Collaborate with cross-functional stakeholders (Quality, Regulatory, R&D, IT) to gather requirements and translate them into system solutions.
  • Ensure compliance with industry regulations (e.g., GxP, FDA, ISO standards) through proper system design and usage.
  • Provide subject matter expertise on QMS processes including CAPA, Change Control, Deviations, Audits, and Document Management.
  • Configure and maintain Veeva Vault modules to support business processes and regulatory requirements.
  • Conduct system validation activities, including documentation, testing, and change control.
  • Support data migration, system upgrades, and integrations with other enterprise systems.
  • Deliver end-user training and provide ongoing support to ensure effective system adoption.
  • Identify opportunities for process improvement and system optimization.
  • Participate in audits and inspections, providing system-related support and documentation.

Requirements
  • QMS Certification (e.g., ASQ, ISO-related certifications, or equivalent).
  • Veeva Certification, specifically related to Veeva Vault (QMS preferred).
  • Proven experience working with Quality Management Systems (QMS) in regulated environments.
  • Hands-on experience with Veeva Vault QMS, including configuration and administration.
  • Strong understanding of GxP compliance requirements and validation processes (CSV/CSA).
  • Experience with quality processes such as CAPA, Change Control, Deviations, and Audits.
  • Excellent analytical, problem-solving, and communication skills.

Qualifications
  • Bachelor or Master's degree in Life sciences or Computer Sciences
  • 5+ years' experience with Computer Systems Validation is required for this role
  • Strong knowledge of GxP Requirements, GLP and GMP regulations, 21 CFR part 11, 210, 211, EU Annex 11, 15 requirements
  • QMS Certification (e.g., ASQ, ISO-related certifications, or equivalent).
  • Veeva Certification, specifically related to Veeva Vault (QMS preferred).
  • Proven experience working with Quality Management Systems (QMS) in regulated environments.
  • Hands-on experience withVeeva Vault QMS, including configuration and administration.
  • Strong understanding of GxP compliance requirements and validation processes (CSV/CSA).
  • Experience with quality processes such as CAPA, Change Control, Deviations, and Audits.
  • Excellent analytical, problem-solving, and communication skills.

Benefits
CURIOSITY DRIVEN, SCIENCE FOCUSED, EMPLOYEE BUILT. Our culture is unlike any other, one where we debate, challenge ourselves, and interact with all alike. We are a curious bunch, characterized by our passion to learn and spirit of teamwork. Zifo is a global R&D solutions provider focused on the industries of Pharma, Biotech, Manufacturing QC, Medical Devices, specialty chemicals and other research-based organizations. Our team's knowledge of science and expertise in technology help Zifo better serve our customers around the globe, including 18 of the Top 20 Biopharma companies.
We look for Science - Biotechnology, Pharmaceutical Technology, Biomedical Engineering, Microbiology etc. We possess scientific and technical knowledge and bear professional and personal goals. While we have a "no doors" policy to promote free access within, we do have a tough door to walk in. We search with a two-point agenda - technical competency and cultural adaptability.
We offer a competitive compensation package including accrued vacation, medical, dental, vision, 401k with company matching, life insurance, and flexible spending accounts.
If you share these sentiments and are prepared for the atypical, then Zifo is your calling!
Zifo is an equal opportunity employer, and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

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