Senior System Validation Engineer

Verista’s 600 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...

*We're excited to welcome new team members, and we're specifically focusing on candidates located in Sunnyvale, CA. This role is strictly open to candidates who are 1099 independent contractors or those who have LLCs. *

As a Senior System Validation Engineer for AG Consulting Partners, a typical day might include the following:

• Performing validation and benchmarking for all cloud shapes, instances, and kernels
• Generating high quality reports for all qualifications and benchmarking cases
• Validating and providing feedback (user experience) on our qualification and benchmarking platform
• Performing qualifications for new hardware, components, firmware, and kernel for on-prem production environments 
• Providing support for our architects by creating documentation and testing runbooks from/for vendors
• Working with vendors and debugging hardware issues found in production and during...

Summary: BioPharma Consulting JAD Group is seeking a talented and experienced Computer System Validation (CSV) Senior Engineer to join our team. As a CSV Senior Engineer, you will play a critical role in ensuring compliance with regulatory requirements and industry standards for computerized systems used in pharmaceutical manufacturing processes. You will lead and execute computer system validation activities and provide expertise in CSV best practices.

Functions: 

• Generate, obtain approvals, and execute validation deliverables for computerized systems and relevant infrastructure, including Validation Plans, Requirements Specification, Risk Assessments, Installation/Operational Qualifications, Traceability Matrices, and Validation Final Reports, ensuring documents meet regulatory and procedural requirements of 21 CFR Part-11, Annex-11 Data Integrity and GAMP5 among others. 

• Plan and organize validation...