IT Business Analyst Regulatory Affairs & PV
Q-Med AB / Datajobb / Uppsala
Observera att sista ansökningsdag har passerat.
Visa alla datajobb i Uppsala,
Östhammar,
Sigtuna,
Österåker,
Håbo eller i
hela Sverige Visa alla jobb hos Q-Med AB i Uppsala,
Stockholm,
Göteborg eller i
hela Sverige We are looking for an IT Business Analyst Regulatory Affairs & PV with expertise in both Information Technology and Regulatory Affairs/Pharmacovigilance. The IT Business Analyst Regulatory Affairs & PV will act as a bridge between senior stakeholders and the IT team. He/She will translate business needs into a functioning set of systems and hardware that will improve Galderma's Regulatory Affairs & Pharmacovigilance systems and overall business performance.
Responsibilities include but are not limited to:
Change Activities
* Integration of new solutions to existing systems
* Master data governance implementation
* Monthly Change Advisory Board meetings to drive evolutions/enhancements to the systems
* System life cycle management (investment strategy, upgrade roadmap, decommissioning
* Establishment of the sustain governance model around the systems
* Business partnership with user representatives to align our service level and activities with business expectations
* Support audits and inspections from regulatory authorities
Project Related Activities
* Plans, organizes and coordinates activities, participate to project plan and resources monitoring (new solutions deployments, upgrades, new regulations)
* Plan, prepare and moderate specifications workshops with business stakeholders in order to translate business requirements/wishes into Specifications
* Assess and execute on new regulatory requirement impact on systems
* Ensure compliance to Data Privacy regulations
Consultant Management
* Be the primary contact from IT for any task executed by external consultants, such as design change request, interface or report setup.
Budget and Procurement
* Comply with purchasing policies, Ensure Purchase Order in place with external consultants
* Ensures sustain costs are included in appropriate budgets, participate to cost tracking versus budget
To ensure success in this role you will have:
* 5 years in IT organization/pharma industry
* Knowledge of GxP and Pharma regulations, Regulatory Affairs/ Operations process and Pharmcovigilance process
* Experience (project management or daily use) with all or some of the following systems: Documentum, D2, RIM solutions (Calyx, ArisG), Argus, Signal Detection,ISI toolbox, EURS Validator
* Scrum expertise is a plus
* Fluency in English is a required, professional proficiency in French or Swedish a plus
* Degree in Computer Science or Information Systems or Life Sciences
Varaktighet, arbetstid
Heltid Permanent
Publiceringsdatum2022-10-20ErsättningNot Specified
Så ansöker duSista dag att ansöka är 2022-11-10
Klicka på denna länk för att göra din ansökanFöretagQ-Med AB
Arbetsgivarens referens Arbetsgivarens referens för detta jobb är "JR003370".
Omfattning Detta är ett heltidsjobb.
Arbetsgivare Q-Med AB (org.nr 556258-6882)
Arbetsplats Galderma
Kontakt Galderma
althea.diazsul@galderma.com Jobbnummer 7091723
Observera att sista ansökningsdag har passerat.