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Veeva Jobs in Georgia (NOW HIRING)

Experience with regulatory and product lifecycle management systems (e.g., PLM, Veeva). * Familiarity with global food regulatory frameworks. Workplace type: Hybrid: This individual will work onsite ...

Experience validating cloud or software as a service platforms, including Veeva, ServiceNow, or Salesforce in a GxP environment * Experience working in Agile delivery environments with validation ...

Experience validating cloud or software as a service platforms, including Veeva, ServiceNow, or Salesforce in a GxP environment * Experience working in Agile delivery environments with validation ...

Amgen Oncology Portfolio Manager - Atlanta, GA

Atlanta, GA · On-site

$100K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... Veeva) on daily basis Penetrate assigned customer targets to the highest levels to build relationships necessary to achieve desired objectives Work cohesively with members of the National Account ...

Experience validating cloud or software as a service platforms, including Veeva, ServiceNow, or Salesforce in a GxP environment * Experience working in Agile delivery environments with validation ...

Showing results 21-40

Veeva information

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$13

$46

$75

How much do veeva jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for veeva in Georgia is $46.17, according to ZipRecruiter salary data. Most workers in this role earn between $32.17 and $59.48 per hour, depending on experience, location, and employer.

What is a Veeva?

A Veeva job typically refers to a role involving Veeva Systems' software, which is used primarily in the life sciences industry for CRM, content management, and regulatory compliance. Professionals in Veeva roles may work as administrators, developers, consultants, or business analysts, focusing on implementing, configuring, or managing Veeva applications like Veeva Vault or Veeva CRM. These roles often require expertise in cloud-based software, data management, and industry-specific regulations.

What are the key skills and qualifications needed to thrive in a Veeva position?

To thrive in a Veeva Specialist or Consultant role, you need a strong understanding of Veeva Vault or Veeva CRM platforms, combined with expertise in life sciences business processes and data management. Familiarity with software configuration, data migration, and certifications like Veeva Vault Administrator or Veeva CRM certification are often required. Excellent problem-solving abilities, communication skills, and the capacity to collaborate effectively with cross-functional teams distinguish top performers in this position. These competencies are critical for supporting efficient system implementations, ensuring compliance, and driving user adoption in regulated industries.

What does a Veeva specialist or consultant do?

As a Veeva Specialist or Consultant, your daily responsibilities may include configuring Veeva Vault or Veeva CRM systems, managing user access, supporting system integrations, and responding to end-user support requests. You'll work closely with business stakeholders to gather requirements, troubleshoot issues, and ensure the software aligns with regulatory requirements in the life sciences sector. Additionally, you might collaborate with project managers, IT, and compliance teams to support new releases or process improvements. This role often requires balancing technical tasks with user training and ongoing documentation.

What are the most commonly searched types of Veeva jobs in Georgia?

The most popular types of Veeva jobs in Georgia are:

What are popular job titles related to Veeva jobs in Georgia?

For Veeva jobs in Georgia, the most frequently searched job titles are:

What job categories do people searching Veeva jobs in Georgia look for?

The top searched job categories for Veeva jobs in Georgia are:

What cities in Georgia are hiring for Veeva jobs?

Cities in Georgia with the most Veeva job openings:

Infographic showing various Veeva job openings in Georgia as of August 2026, with employment types broken down into 83% Full Time, 4% Part Time, 2% Temporary, and 11% Contract. Highlights an 74% Physical, 8% Hybrid, and 18% Remote job distribution, with an average salary of $96,044 per year, or $46.2 per hour.

Quality Management Specialist with Security Clearance

Lukos

Atlanta, GA • On-site

Other

Posted 14 days ago


Job description

Position: 
Quality Management Specialist
Location: 
Atlanta, GA
Job Id: 
2205
# of Openings: 
1 Quality Management Specialist Minimum Qualifications Summary Certification & Education * Bachelor’s Degree (B.S.) in a related scientific discipline with 5–8+ years of progressive experience managing quality systems in clinical or public health laboratories.
* Master’s Degree Preferred
Experience Required * In-depth, working knowledge of CLIA regulations (42 CFR Part 493) for high-complexity testing, as well as CLSI guidelines. * Hands-on experience building, implementing, and maintaining a QMS mapped directly to the CLSI 12 QSE model (Organization, Process Control, Equipment, Assessment, Occurrence Management, etc.) with CDC’s Quality Manual for Microbiological Laboratories (QMML), BSL-2/BSL-3 containment practices, and ISO standards (such as ISO 15189 or ISO 17025).
* Practical experience administering electronic Quality Management Systems (eQMS) such as MasterControl, Qualio, Veeva, or proprietary federal/CDC eQMS platforms.
* Proven track record in drafting, reviewing, archiving, and controlling Standard Operating Procedures (SOPs), policies, forms, and revision histories under strict change-control rules.
* Experience logging, investigating, and resolving Nonconformance Events (NCs), deviations, and out-of-specification (OOS) results.
* Proficiency using structured Root Cause Analysis (RCA) tools (e.g., 5 Whys, Fishbone/Ishikawa diagrams) to develop and monitor Corrective and Preventive Actions (CAPAs).
* Hands-on experience creating audit checklists, scheduling, conducting internal quality assessments, and reporting findings for both clinical and research laboratory workflows.
* Experience preparing laboratories for external accreditation audits (e.g., CLIA, CAP, ISO, or CDC internal oversight).
* Experience coordinating vendor service calls, managing preventative maintenance (PM) schedules, equipment calibrations, and maintaining equipment logbooks.
* Familiarity with vendor contracting, obtaining quotes, and navigating institutional or federal procurement systems (e.g., CDC purchasing workflows and requisition portals implied by this contract specification). Job Objective Lukos seeks a Quality Management Specialist seeking to leverage expertise in CLIA regulations, CDC QMML standards, and the 12 Quality System Essentials (QSEs) to drive compliance and operational excellence in clinical and research laboratories. Proficient in managing eQMS document control, conducting root-cause nonconformance investigations (CAPA), and leading internal quality assessments. Adept at administering equipment maintenance logistics, vendor contracts, and cross-functional communication to maintain seamless laboratory operations. Committed to delivering rigorous regulatory adherence, process optimization, and constant audit readiness within high-complexity laboratory environments. Responsibilities * Collaborate with the quality manager and safety manager as a team to implement and manage QMS and CLIA.
* Maintain current knowledge of the status, issues, training, and progress related to the Quality Management System (QMS), CDC’s Quality Manual for Microbiological Laboratories (QMML), Clinical Laboratory Improvement Amendments (CLIA), Clinical and Laboratory Standards Institute (CLSI), and other applicable national and international standards, including their implementation and ongoing maintenance.
* Ensure and manage the effective implementation of quality policies, processes, and procedures utilizing the 12 Quality System Essentials (QSEs).
* Perform document control and support the management of quality-related procedures and forms.
* Maintain, update, and track documents and records utilizing CDC’s electronic quality management system (eQMS).
* Coordinate and communicate with branch personnel and relevant CDC offices regarding procedures, schedules, and related matters.
* Perform administration of equipment maintenance and calibration activities, including obtaining vendor quotes, submitting and managing forms and requests through CDC’s applicable purchase systems, and arranging vendor service calls.
* Investigate nonconformance events and develop and implement corrective actions.
* Conduct quality assessments in accordance with quality review plan criteria to evaluate compliance with applicable research and clinical laboratory policies, processes, procedures, and standards.  Education & Certification * Bachelor’s Degree (B.S.) in a related scientific discipline with 5–8+ years of progressive experience managing quality systems in clinical or public health laboratories.
* Master’s Degree Preferred
Work Location Atlanta, GA About Lukos Lukos delivers professional services to the Department of Defense. Lukos has been one of the most successful and most diversified support companies for US Special Operations Command and its components for over a decade. Since our founding, we have grown to support all military services and multiple federal civilian agencies. About Our Name: Lukos is ancient Greek for “wolf”. The characteristics of the wolf match our approach to national security. The wolf is known for cunning, aggression, patience, and teamwork. An individual wolf is smart, strong, and resilient, but the true strength of wolves is their ability to work together as a wolfpack. Kipling said it best in The Law of the Jungle. "For the strength of the pack is the wolf, and the strength of the wolf is the pack." Lukos is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, disability, or national origin. Apply for this Position

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About Lukos

Sourced by ZipRecruiter

Industry

Guided missile and space vehicle manufacturing

Company size

51 - 200 Employees

Headquarters location

Tampa, FL, US

Year founded

2008

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