Validation Systems Administrator

Job not on LinkedIn

🔥 6 minutes ago

❄️ Minnesota – Remote

❄️ Minnesota – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

⌨️ Systems Administrator

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

Dayforce

WebsiteLinkedInAll Job Openings

5001 - 10000 employees

👥 HR Tech

☁️ SaaS

🤝 B2B

💰 $1G Post-IPO Debt - Dayforce on 2024-03

HR Tech • SaaS • B2B

Dayforce is a cloud-based human capital management (HCM) platform that provides payroll, workforce management, HR, benefits, talent management, and analytics to employers. Delivered as a software-as-a-service solution, Dayforce consolidates time and attendance, scheduling, payroll, and HR functions into a single application aimed at medium and large organizations to streamline workforce processes and compliance.

📋 Description

• Responsible for the day-to-day administration and configuration of the Kneat eValidation system across all Kindeva sites. • Create, update, and modify Kneat templates, document types, and document packs for all Kindeva sites. • Set up and maintain workspaces and disciplines in Kneat for all Kindeva sites. • Perform user management activities including account creation, role assignments, access modifications, and periodic access reviews. • Execute and document validation lifecycle activities using Kneat workflows under guidance from the validation team. • Provide day-to-day end-user support and troubleshooting for Kneat configuration issues. • Support Kneat system release updates by reviewing release notes. • Collaborate with Quality, IT, Engineering, and Manufacturing teams to ensure compliant system use. • Assist in training and onboarding users in Kneat functionality and best practices for compliant use. • Support inspection readiness activities by ensuring Kneat records, audit trails, and system documentation are complete and accurate. • Ensure system compliance with GxP, 21 CFR Part 11, EU Annex 11, and other applicable regulations.

🎯 Requirements

• Bachelor’s or Master’s degree in Engineering, Life Sciences, Pharmacy, or related field preferred. • 2+ years of experience in validation, quality systems in the pharmaceutical, medical device or biotechnology industry • Hands-on experience with the Kneat eValidation platform, including template creation, workspace configuration, and user management. • Excellent problem-solving, communication, and organizational skills. • Ability to work independently and in a global, cross-functional team environment. • Hands on experience with GMP computerized systems, including system validation and regulatory compliance. • Working knowledge of GMP computerized systems, 21 CFR Part 11, and EU Annex 11 requirements in a regulated manufacturing environment. • Kneat admin certification preferred (or willingness to obtain upon hire) • Familiarity with GMP regulatory requirements and the importance of data integrity in a validated system.

🏖️ Benefits

• CDMO experience is a plus, with exposure to supporting multiple clients, projects, or validation strategies within Kneat‑supported environments.