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VeristaVE

6283 - IT CSV Engineer / Sr. Validation Engineer

Verista is a leading business and technology consultancy firm providing systems, compliance, validation, and quality solutions to life science companies, enabling them to improve health and lives. They assist clients with critical challenges across the GxP lifecycle, from research and development to commercialization and manufacturing.

Verista

Employee count: 501-1000

Salary: 70k-114k USD

United States only

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Description

Verista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world’s most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities.

Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.

Company Culture Guidelines & Values:

  • We empower and support our colleagues
  • We commit to client success at every turn
  • We have the courage to do the right thing
  • We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged.
  • We constantly acquire new skills and learn from our experiences to enhance our collective expertise

The IT CSV Validation Engineer is responsible for authoring and executing validation test scripts to support regulated systems within a GxP life sciences environment. This role will focus on validating ERP Master Data Governance platforms and system integrations, ensuring compliance with regulatory requirements and data integrity standards.

IT CSV Engineer Responsibilities:

  • Author, review, and execute validation test scripts (IQ/OQ/PQ) for GxP computerized systems
  • Perform validation of ERP Master Data Governance platforms and associated system interfaces, including data ingestion, transformation, and reporting layers
  • Collaborate with cross-functional teams (IT, QA, Business, Data Engineering) to define validation scope, risk assessments, and acceptance criteria
  • Ensure compliance with GxP, 21 CFR Part 11, and data integrity requirements throughout the system lifecycle
  • Support deviation investigations, CAPAs, and change control activities related to validated systems
  • Maintain validation documentation including Validation Plans, Risk Assessments, Traceability Matrices, and Summary Reports

Job Requirements:

  • Bachelor’s degree in Computer Science, Engineering, Life Sciences, or related discipline
  • 5+ years of Computer System Validation (CSV) experience in pharmaceutical or life sciences environments
  • Strong experience with test script authoring and execution for GxP systems
  • Experience validating ERP Master Data Governance platforms and system interfaces (SAP preferred)
  • Familiarity with AI/advanced data platforms is a plus
  • Experience with validation management tools such as ValGenesis is a plus
  • Strong understanding of GxP, 21 CFR Part 11, and data integrity principles
  • Ability to work independently and manage multiple validation activities with minimal oversight

For US geography, the salary range for this position is shown below. The actual salary is dependent upon a variety of job-related factors such as professional background, training, work experience, location, business needs, market demand, and competitive market practice. Therefore, in some circumstances, the actual salary could fall outside of this expected range. This salary range is subject to change and may be modified in the future.

*Verista is an equal opportunity employer.

National (US) Range
$70,491—$113,521 USD

Benefits

Why Choose Verista?

  • High growth potential and fast-paced organization with a people-focused culture
  • Competitive pay plus performance-based incentive programs
  • Company-paid Life, Short-Term, and Long-Term Disability Insurance.
  • Medical, Dental & Vision insurances
  • FSA, DCARE, Commuter Benefits
  • Supplemental Life, Hospital, Critical Illness and Legal Insurance
  • Health Savings Account
  • 401(k) Retirement Plan (Employer Matching benefit)
  • Paid Time Off (Rollover Option) and Holidays
  • As Needed Sick Time
  • Tuition Reimbursement
  • Team Social Activities (We have fun!)
  • Employee Recognition
  • Employee Referral Program
  • Paid Parental Leave and Bereavement

Verista collects and processes personal data in accordance with applicable data protection laws. If you are a California Job Applicant, see the privacy notice for further details.

For more information about our company, please visit us at Verista.com

About the job

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Posted on

Job type

Full Time

Experience level

Salary

Salary: 70k-114k USD

Education

Bachelor degree

Experience

5 years minimum

Location requirements

Hiring timezones

United States +/- 0 hours

About Verista

Learn more about Verista and their company culture.

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Verista's journey began with the unification of three established and respected firms: Clarke Solutions, Covex LLC, and Acquire Automation. Recognizing the growing and evolving needs of the life sciences industry, these companies came together in 2020 to form Verista, a powerhouse of expertise and comprehensive solutions. Clarke Solutions brought a strong foundation in engineering and automation solutions for manufacturing environments, a journey that started over two decades prior. Covex LLC, founded in 2001 by Rich Murg, contributed significant experience in compliance services, growing to become a leading provider in that space before being acquired and merged to form Verista. Acquire Automation added further depth in automation and packaging solutions. This strategic consolidation was driven by the vision to create a single, trusted partner that could support clients across the entire GxP lifecycle, from the initial stages of research and development through to commercialization, manufacturing, and distribution.

Since its inception, Verista has focused on bridging the traditional gap between IT and operations, offering a unique blend of industry-specific knowledge, subject-matter expertise, and collaborative approaches rooted in best practices and repeatable processes. The company has steadily grown, expanding its team to over 700 experts dedicated to delivering consistent, safe, and high-quality results. This growth has been fueled by a commitment to understanding the intricate challenges faced by pharmaceutical, biotech, and medical device companies, including navigating complex regulatory landscapes, meeting aggressive timelines, and managing budget constraints. Verista's evolution has been marked by a dedication to empowering the scientific community and helping organizations solve critical healthcare challenges by providing innovative solutions and services that enable informed decision-making. The company continues to invest in its people and capabilities, fostering a culture of continuous learning, client focus, and integrity to ensure it remains at the forefront of the life sciences consulting industry.

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