> Markdown version of [/jobs/ext/4460623-assoc-automation-systems-administrator](https://www.wearedevelopers.com/jobs/ext/4460623-assoc-automation-systems-administrator). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Assoc Automation Systems Administrator - **Company:** Regeneron - **Location:** Rensselaer, NY, United States - **Experience:** Starter - **Salary:** $62,355.0 - $92,400.0 - **Contract:** Permanent contract - **Skills:** Spreadsheets, Configuration Management, Databases, System Configuration, Local Security Policy, Microsoft PowerPoint, Software Systems, System Software, Process Control Systems - **Published:** October 14, 2026 - **Apply:** https://www.indeed.com/viewjob?jk=13a13f1f1d4d6c62 ## About the Role BS/BA in Science/Engineering or related field preferred along with 1-2 years of relevant experience in manufacturing/lab/IT setting; will consider minimum 3 years of relevant experience in manufacturing/lab/IT setting in lieu of educational requirement. Knowledge Skills, and Abilities: * Working knowledge of process control systems and product release testing systems preferred. * Current knowledge of cGMP biotech/pharma operations, regulatory and quality policies, procedures and documentation methods. * Knowledge of Risk Assessments * Must work independently and have project team member capabilities. * Knowledge of biotech/pharma manufacturing process/supporting laboratory testing and regulatory requirements, related terminology and jargon commonly used in association with daily operations of a facility and the ability to use the terminology, in context, when discussing issues or generating documentation. * Excellent writing, communication and interpersonal skills. * Working knowledge of word processing, spreadsheet, PowerPoint and database management software. ## Description * Ensure systems' data is backed up / archived as required to ensure system can meet defined RTO and RPO. Perform recovery of data as needed. * Configuration management and recipe/method management per procedure. * Documents system configurations for cGMP software for process control, monitoring and testing. * Support system SAT/FAT, validation and qualification efforts. * Supports review of system lifecycle design documentation * Process change control requests for system configurations, including requirement and/or design specifications, test plans, technical evaluation and quality risk assessments. * Follow relevant system software SOPs and policies. * Provide end-user support including troubleshooting problems at the application level and basic hardware troubleshooting (includes working with vendors to resolve issues). * Support Change Controls, NOE's, risk assessments, impact statements and corrective/prevention action plans. Assist with investigations and root cause analysis for department issues of non-compliance. * Administer user access - Control access to software systems; add, modify and remove users; define user types, user groups and security settings per procedure.