Sr. Configuration Manager

Position Summary The Sr Configuration Manager reports to the Director of Validation. The position is responsible for defining and executing programming to support software controlled and laboratory data systems within the facility from an administration and software technical support perspective.  The position will be primarily responsible for laboratory equipment data systems support. This role supports Catalent's Patient First Philosophy by Engaging in all aspects of new product development and maintaining and managing systems The Role Serve as the primary point of contact with Global IT for any server or system changes that could affect laboratory operations (Active directory, server/software updates, IP Address changes, system back-up etc.) Routinely monitor status of all laboratory data systems to ensure systems running efficiently and compliantly. Work with global IT to remove or add instruments to systems as necessary and ensure connections to servers are maintained. On boarding of new products, methods, and reporting templates to the QA data systems. Administration and tech support for software controlled systems, including LabX, Empower, Nugenesis, and laboratory instrument specific data systems. Lead and assist to Debug and troubleshoot issues with laboratory equipment and data systems. Note: Catalent Woodstock is a 24/7 operation.  This position will often require technical support remotely and/or onsite during hours outside of normal office hours.   The Candidate Bachelor's degree in Information Technology or Engineering or related discipline.  Master's degree a plus. 3 - 5 years of Quality data systems administration and/or IT experience. Strong IT and/or laboratory data systems background is required with preferred laboratory experience. Familiarity with EmPower, Nugenesis, and/or LabX data systems is highly desirable.   Familiarity with laboratory instruments/processes such as HPLCs, UV, Titrators a plus. Knowledge of TCP/IP and databaseexperience highly desirable. S.O.P. writing and/or training experience a plus. Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulatory requirements preferred Experience with FDA related computerized systems/software validation. Experience with FDA part 11 compliant systems. Successful candidates will possess Catalent's standard leadership competencies that are used to interview and for Performance & Development: Leads with Integrity and Respect Delivers Results Demonstrates Business Acumen Fosters Collaboration and Teamwork Champions Change Engages and Inspires Coaches and Develops Position Benefits Medical, Dental, Vision and 401K are all offered from day one of employment 19 days of paid time off annually Potential for career growth within an expanding team Defined career path and annual performance review and feedback process. 0028787
Salary Range: NA
Minimum Qualification
Less than 5 years

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