Xyntek Inc · 5 days ago
Quality Assurance Computer System Validation
West Point, Pennsylvania, United States
Full-time
Onsite
Senior Level
5+ years expXyntek Inc is seeking a Quality Assurance Computer System Validation (CSV) professional to ensure compliance and efficiency of computerized systems within their new facility. The role involves providing quality assurance support for SDLC deliverables, collaborating with teams for risk-based validation activities, and leading validation teams in best practices.
Industrial AutomationLife SciencePharmaceutical
Responsibilities
Responsible for providing quality assurance support and oversight for System Development Life Cycle (SDLC) deliverables of primarily Laboratory Instrument Systems and secondary for Application Systems support GxP operations
Collaborate with cross-functional team to define risk-based approaches for computer system validation activities and testing
Lead validation teams to a better understanding of validation best practices and applying quality principles
Reviews various GxP deliverables for conformance with SDLC baseline criteria and other internal and external regulations
Identifies and resolves issues interfering with execution of deliverables
Enforces Good Documentation Practices and ensures that SDLC deliverables are properly cataloged and available for internal and external regulatory inspection
Provide additional support with SDLC deliverables for Enterprise Application support, as applicable
Perform Supplier Assessments to ensure vendor compliance to regulations and standards before introducing instruments or applications into the lab environment
Attend meetings as quality representative and capture meeting minutes, escalating items as appropriate
Oversee team’s progress and accomplishments on instrument validation activities ensuring project remains on target for key milestones
Qualification
Required
5-8 years of experience working in a Pharmaceutical/Biotechnology industry; experience working in a health authority regulated (e.g. GxP) environment
Industry experience including computer system validation, System Life Cycle (SLC), software validation, and/or Quality Assurance functions
High level of expertise and exposure with agency regulations, such as 21 CFR Part 11, Part 58, Part 210, Part 211 from the US Food and Drug Administration
High level of expertise in SLC methodology (e.g., V-model, waterfall, agile, spiral) including change management
Extensive experience providing oversight for adherence to enterprise SLC and procedures
Experience in creation, execution, and reviewing a change control document
Proficient skills dealing with and understanding typical laboratory facilities and equipment
Ability to prioritize and manage multiple initiatives, projects concurrently
Benefits
Total Rewards package
Great personal benefits
Professional growth opportunities
Equal Opportunity Employer
Assistance with Critical Skills Visa applications for eligible candidates
Company
Xyntek Inc
As part of CXV Global, we offer a powerful platform of combined technologies and professional services that optimise life sciences’ and high-end operations across product development, manufacturing, packaging and distribution.
501-1000 employees
H1B Sponsorship
Xyntek Inc has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (1)
2023 (1)
2022 (2)
2021 (2)
Funding
Current Stage
Late StageCompany data provided by crunchbase