IT System Manager III - Multiple Openings
- Systems Management:
- Ensures system compliance with relevant internal SOPs & guidelines as well as external requirements (21CFR Part 11, Personal Data Protection, SARBOX, etc.)
- Reviews & maintains all IT CSV validation/system decommissioning documentation in accordance to regulatory & Novo Nordisk requirements
- Responsible for the system life cycle management & suggests inputs for the IT roadmap
- Documents operation & maintenance of the system (incident management, contract/SLA management, data integrity/retention/archive, continuity/recovery plans)
- Performs system reviews to ensure basic IT controls are in place & in control to ensure compliance/security of the system
- Acts as a peer mentor & lead in reviewing documentation prepared by team members
- Review & approves testing protocols to ensure requirements are tested appropriately
- Participates in root cause analysis for deviations within supported IT Systems to ensure effective corrective actions are identified & implemented
- Audit & inspection support
- Documentation:
- System documentation including operational manuals, system architecture, & data flow completion
- Works with subject matter expert (SME) to ensure system documentation is in compliance with local, corporate & regulatory regulations
- Documentation of system configuration baselines
- Security:
- Approves appropriate access to new users & removes access as necessary
- Works with IT Security/SME to ensure controls are in place & documented
- Performs annual system evaluation
- System Support:
- Serves as the escalation point for system support
- Ensures end user training is in place, as required
- Prepares support agreements with internal & external sources
- System Projects:
- Ability to lead projects & project teams as needed. Performs activities assigned within agreed timelines
- Other accountabilities, as assigned
- Bachelor's Degree in Computer Science or Engineering, or similar applicable technical degree in relevant field required
- Minimum seven (7) years of operation & maintenance of IT systems preferably within the pharmaceutical industry required
- Experience with production manufacturing; IT projects & management of IT systems required
- Understanding of & knowledgeable in the following areas: IT frameworks such as COBIT, ITIL, GAMP, 21CFR Part 11, &/or PIC/S Annex 11. System development lifecycle including validation of computer systems, operation & maintenance, & decommissioning of systems. Manufacturing processes for manufacturing areas (aseptic, inspection, assembly, packaging, utilities, & laboratories). Required
- Expert in GxP documentation practices required
- Proficient in basic computer skills including experience with Microsoft Office preferred
- Ability to independently review & approve protocols & technical documents in compliance with regulatory & Novo Nordisk requirements required
- Excellent oral & written communication skills preferred
- Experience in regulatory audits & inspections preferred
- Experience in project teams driving deliverables, tasks, & activities for computer system validation required
- Expert in utilizing appropriate root-cause analysis tools & techniques preferred
- Demonstrated expertise in planning/organizing, managing execution, checking results, & revising the work plan for complex problems being resolved by cross functional teams preferred
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