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Business Process Manager (BPM)

Eingestellt von DWI Consulting Ltd

Gesuchte Skills: Design, Aris

Projektbeschreibung

BUSINESS PROCESS MANAGER (BPM) PHAMA

We are currently looking for a Business Process Manager (BPM) within the Pharmaceuticals sector. You will be responsible for implementation, improvement and design of projects related to the procedural framework for GxP (good practices) and business processes. You will have to design and implement Role Risk based training plans and contribute to the development of a quality system that enables the Global Clinical Development Organization (GCDO) to conduct clinical trials in an efficient and compliant way, resulting in clinical programs that allow for seamless registration of the compounds.

Lead or participate in improvement projects to describe the new desired state of processes for compliance. Gather and analyse metric. You will oversee detailed process development, procedural document development, training development in collaboration with the responsible functions to ensure content and requirements of the design are fully transferred and implemented.

The BPM will create high level process maps in ARIS and provide sufficient detail to ensure all levels of the process can be worked out. Create detailed process flows for selected projects. Review detailed process flows and approve through agreed stage-gate and versioning approaches. Develop the associated training material and have it deployed to the relevant target audience applying a role risk based training methodology.

Good Ability to interpret data to develop action plans to improve business. Strong networking and relationship building skills; Ability to create an open and inviting environment. Experience in R&D process requirements to successfully drive Q&C productivity, strategy optimization. Ability to translate data into information and strategies into executable action plans. Experience in quality activities, including audits of clinical investigative sites, compliance support and audits of regulatory submissions is an asset

EDUCATION

Masters degree or BS/BA with minimum of 8 years' experience in a medium to large scale Matrix organization which includes applicable compliance related field and/or equivalent time and experience in a related R&D area is required. Requires knowledge of the drug development process, good knowledge of worldwide GxP compliance regulations, sound research and development practices, scientific and quality terminology, company quality assurance procedures and policies, and quality evaluation techniques as well as adult training development expertise.

Projektdetails

  • Einsatzort:

    Antwerpen, Belgien

  • Projektbeginn:

    asap

  • Projektdauer:

    6 months (+ Extension)

  • Vertragsart:

    Contract

  • Berufserfahrung:

    Keine Angabe

Geforderte Qualifikationen

  • Kategorie:

    IT Entwicklung, Medien/Design

  • Skills:

    design, aris

DWI Consulting Ltd