6275 - IT CSV Engineer / Sr. Validation Engineer
About The Position
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 processes and Data Lake platforms, ensuring compliance with regulatory requirements and data integrity standards.
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 supporting Master Data Governance processes (SAP experience preferred but not required)
- Experience validating Data Lake environments and system interfaces (Snowflake experience preferred)
- Strong understanding of GxP, 21 CFR Part 11, and data integrity principles
- Ability to work independently and manage multiple validation activities with minimal oversight
Nice To Haves
- Familiarity with AI/advanced data platforms is a plus
- Experience with validation management tools such as ValGenesis is a plus
Responsibilities
- Author, review, and execute validation test scripts (IQ/OQ/PQ) for GxP computerized systems
- Support validation activities for ERP Master Data Governance processes, ensuring data accuracy, integrity, and compliance
- Perform validation of Data Lake 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
Benefits
- 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
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Number of Employees
101-250 employees
