IT Systems Manager managing life cycle, compliance, and project oversight of IT systems for pharmaceutical industry. Collaboration with stakeholders and regulatory adherence vital.
Responsibilities
Manage systems throughout their lifecycle, provide project oversite and drive deliverables, partner with key stakeholders, & ensure adherence to the Novo Nordisk and regulatory requirements for assigned IT Systems.
Ensure processes are in place for system maintenance & operation according to relevant regulatory authorities (GxP, financial, personal data protection, etc.)
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 providing reviews and input to documentation prepared by other team members
Ensures appropriate testing (i.e., FAT, SAT, UAT, IQ, OQ, PQ, &/or GEP) is in place to ensure IT requirements are met
Participates in root cause analysis for deviations within supported IT Systems to ensure effective corrective actions are identified & implemented
Represents IT systems in connection with audits and inspections
Works with subject matter expert (SME) to ensure system documentation is compliant with local, corporate & regulatory regulations
Approves appropriate access to new users & removes access as necessary
Serves as the escalation point for system support
Ensures end user training is in place, as required
Prepares support agreements with internal & external sources
Performs activities assigned within agreed timelines
Requirements
Bachelor's Degree in Computer Science or Engineering, or similar applicable technical degree in relevant field required
Minimum five (5) years of operation & maintenance of IT systems preferably within the pharmaceutical industry required
Experience with production manufacturing; IT projects & management of IT systems required
Knowledgeable & have an understanding in the following areas: required IT frameworks such as COBIT, ITIL, GAMP, 21CFR Part 11, &/or PIC/S Annex 11 required
System development lifecycle including validation of computer systems, operation & maintenance, & decommissioning of systems required
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 required
Ability to independently review & approve protocols & technical documents in compliance with regulatory & Novo Nordisk requirements required
Excellent oral & written communication skills required
Experience in regulatory audits & inspections required
Experience in project teams driving deliverables, tasks, & activities for computer system validation required
Expert in utilizing appropriate root-cause analysis tools & techniques required
Demonstrated expertise in planning/organizing, managing execution, checking results, & revising the work plan for complex problems being resolved by cross functional teams required
Benefits
Leading pay and annual performance bonus for all positions
All employees enjoy generous paid time off including 14 paid holidays
Health Insurance, Dental Insurance, Vision Insurance – effective day one
Guaranteed 8% 401K contribution plus individual company match option
Family Focused Benefits including 14 weeks paid parental & 6 weeks paid family medical leave
Free access to Novo Nordisk-marketed pharmaceutical products
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