REQ : Chromeleon System Administrator in Cincinnati, OH. (Onsite Position)
Why This Role Stands Out
This role offers a fantastic opportunity to deepen your expertise as a Chromeleon System Administrator within a reputable consulting firm. If you thrive in a collaborative, onsite environment and are eager to contribute to impactful technology solutions, this position is an excellent fit for your career growth. We encourage you to apply and explore this exciting opportunity!
Quick Overview
Job Description
Hi,
One of our clients is looking for Chromeleon System Administrator in Cincinnati, OH. (Onsite Position)
Title: Chromeleon System Administrator
Location: Cincinnati, OH. (Onsite Position)
Duration: 12 Months
C2C or W2 Only
Role Summary:
We are seeking an experienced Chromeleon System Administrator (L2/L3 Support) to develop, enhance, integrate, and support enterprise Chromeleon Chromatography Data System (CDS) applications. The ideal candidate will have hands-on experience with the Chromeleon SDK, laboratory informatics systems, SQL database development, and enterprise application support within regulated pharmaceutical or life sciences environments.
The role involves application development, system integration, incident resolution, change implementation, and ongoing support of Chromeleon-based laboratory applications while ensuring compliance with GxP and enterprise IT standards.
Required Skills & Qualifications:
Education:
- Bachelor's degree in Computer Science, Software Engineering, Information Technology, or a related field.
Technical Skills:
- 4–8+ years of experience in enterprise application development and support.
- Hands-on experience with Chromeleon SDK development and customization.
- Strong SQL development and database design skills.
- Experience integrating laboratory applications such as Chromeleon and LIMS.
- Experience working in Agile or DevOps environments.
- Strong analytical and debugging skills.
- Excellent written and verbal communication skills.
Preferred Skills:
- Experience in pharmaceutical, biotechnology, or life sciences organizations.
- Knowledge of GxP, FDA 21 CFR Part 11, ALCOA+, and CSV (Computer System Validation).
- Experience with C#, .NET Framework/.NET Core, or other enterprise development technologies.
- Experience with Azure DevOps, Git, or similar version control tools.
- Exposure to CI/CD pipelines and automated deployments.
- Knowledge of PowerShell scripting.
- ITIL Foundation certification.
Tech Stack:
- Chromeleon CDS & Chromeleon SDK
- C#, .NET Framework/.NET Core
- REST APIs & System Integration
- Microsoft SQL Server (T-SQL, Stored Procedures, Views)
- Nexus LIMS Integration
- Microsoft Azure
- Citrix Virtual Apps & Desktops
- Windows Server Administration
- Veeva Vault
- IBM BigFix
- Git / Azure DevOps (Preferred)
- PowerShell
- GxP, FDA 21 CFR Part 11 & Computer System Validation (CSV)
Soft Skills:
- Strong problem-solving and analytical skills
- Ability to work in global, cross-functional teams
- Excellent communication and stakeholder management
- Ability to handle multiple priorities in a fast-paced environment
Key Responsibilities:
- Provide L2/L3 application development and production support for Chromeleon CDS applications.
- Design, develop, enhance, and maintain solutions using the Chromeleon SDK.
- Develop integrations between Chromeleon, Nexus LIMS, and other enterprise laboratory systems.
- Analyze business requirements and translate them into scalable technical solutions.
- Develop and maintain SQL scripts, stored procedures, queries, and database objects.
- Troubleshoot complex application issues and perform root cause analysis (RCA).
- Support application deployments, upgrades, patches, and release activities.
- Collaborate with laboratory users, business analysts, infrastructure teams, and vendors to deliver application enhancements.
- Manage incidents, defects, and change requests using ServiceNow (SNOW).
- Create and maintain technical documentation, knowledge articles, and SOPs using Veeva and ServiceNow.
- Participate in application testing, validation, and production release activities.
- Ensure applications comply with GxP, FDA 21 CFR Part 11, and internal quality standards.
- Perform performance tuning and optimization of application and database components.
- Support application lifecycle management, including development, testing, deployment, and maintenance.
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