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SAP Business Analyst - GxP/Regulatory/Drug Development Process

Eingestellt von ITech Consult

Gesuchte Skills: Sap, Usability, Design

Projektbeschreibung

SAP BUSINESS ANALYST - GXP/REGULATORY/DRUG DEVELOPMENT PROCESS

ABOUT US:ITech Consult AG is a certified ISO 9001/2008 Swiss company with offices also located in Germany, Great Britain and Ireland. ITech Consult is specialised in delivering ICT candidates for contract work. We were founded in 1997 by IT professionals; hence we well understand what it means to be professionally supported in your search for a new project and being employed.

REFERENCE NO.:916729NC
Role: SAP Business Analyst - GxP/Regulatory/Drug Development Process
DOMAIN: Regulatory/Pharma/Drug
LOCATION: Basel und Region, SwitzerlandWORKLOAD: 100%
START DATE: ASAP
DURATION: Till 29/12/2017

RESPONSIBILITIES:
-Leading business requirements sessions for a functional/process area topic with a team of business users including: utilizing necessary analytical tools that result in aligned concepts, business processes and requirements with the business team
-Providing guidance to the business team to ensure consistency of the overall solution, continuous management of user expectations.
-Owning and managing user requirements specifications for a functional area, ensuring that the complexity of the requirements is documented in concise, scalable manner that is easily understood by both the business team and vendor team
-Owning the delivery of requirements for a functional area including: providing continuous clarifications to vendor team on requirements during build, and validating the implementation of requirements from a usability perspective.
-Ability to discuss and negotiate and agree on proposed design options with key stakeholders in the organization

Required Skills:
-Minimum 8 Years of experience in SAP
-Minimum 5+ plus years of experience in business analysis
-Good experience of analysing business needs, eliciting and documenting effective user requirements for GxP system
-Experience working with global teams

Nice to Have:
-Good Knowledge of Drug Development Process.
-Regulatory domain knowledge (specifically submission and registration management)

Languages:
-English Fluent
-German Fluent is plus

SHOULD YOU FIND YOURSELF SUITABLE FOR THIS POSITION THEN SEND YOUR COMPLETE DOSSIER USING THIS LINK IN THE ADVERT.

*EVEN IF THIS POSITION DOESN'T SUIT YOUR PROFILE WE RECOMMEND THAT YOU SEND US YOUR CV AND SHARE WITH US WHAT YOU ARE EXACTLY LOOKING FOR.

CALL US AND DISCOVER THE QUALITY OF OUR SERVICES FOR YOURSELF. WE ARE MORE THAN HAPPY TO MEET WITH YOU FOR AN INDIVIDUAL CONSULTATION. DO NOT HESITATE TO CONTACT US FOR FURTHER ENQUIRES

OUR PAY ROLLING IS REFERRED BY 98% OF OUR FREELANCERS AS THE BEST PAY ROLLING SYSTEM IN SWITZERLAND. DO YOU REQUIRE MORE INFORMATION? FEEL FREE TO CONTACT US.

Projektdetails

  • Einsatzort:

    Basel, Schweiz

  • Projektbeginn:

    asap

  • Projektdauer:

    Till 29.12.2017

  • Vertragsart:

    Contract

  • Berufserfahrung:

    Keine Angabe

Geforderte Qualifikationen

ITech Consult