Hi Associate,
We have an Urgent opening .Please see the Job Description Below and let me know if you have any consultant available. *Title: -* *Business System Analyst- Biopharmaceutical Domain* *Location: - Thousand Oaks, CA* *Duration:- 6 months+(Contract)* *Job Summary:* The IS Business System Analyst works within the Development Information Systems (DevIS) group to support transformational IS initiatives for regulated document management and submission dossier management across multiple functional areas. The IS Business Analyst acts as an intermediary between the initiative work streams and affected business clients to elicit, clarify, and translate business requirements into documentation and conceptual design (using appropriate tools and models) from which applications and solutions will be developed. Contributes to the success of the business by defining fundamental improvements in how information is managed and business processes are operated. Leverages the combination of prior experience, problem solving skills, and client engagement skills to drive our business towards excellence. Is a keen learner and thrives in dealing with ambiguity. o Serves as a key IS contact for business partners to provide expertise in business requirements reviews, research new applications and services to improve business capabilities o Lead requirements elicitation workshops with business and technology partners to elicit, analyze, translate, and document business requirements into functional and non-functional requirements o Identify key data (information) objects that support the affected business process(es), determine data objects used by each business process, identify data objects to be utilized by multiple applications and how they are to be shared/interfaced o Serve on project teams and assist with workshop planning and facilitation as well as project deliverable production o Define opportunities for, plan, and support proof-of-concepts to help the business evaluate the feasibility of new technology as needed o Perform cross system analysis, feasibility analysis, scope projects, prioritize deliverables, and recommend optimal solution o Assist with technology solution evaluation and recommendation o Escalate as appropriate problems and issues to management *Preferred Qualifications * o Experience in the Regulatory Affairs process within a biopharmaceutical development organization, including a solid understanding of regulated document management and regulatory submission dossier management business processes o Experience with deploying latest generation of Enterprise Document Management (EDM), regulatory submission dossier management, and Structured Content Management (SCM) systems o Self-starter with a high degree of initiative o Consulting experience or management consulting experience highly preferred o Solid understanding of business process mapping, requirements elicitation and management, agile software development o Ability to prioritize and manage multiple tasks o Team-oriented, placing priority on the team’s success o Excellent verbal, written, and interpersonal communication skills o Strong communication and presentation skills and ability to communicate with Business users in non-technical language o Strong leadership and organizational change management skills · Highly analytical with attention to detail Thanks & Regards *Wasim Ahmed* Phone : 609-853-0818 X 2178 Fax : 609 799 5746 Email: wasim.ah...@nityo.com www.nityo.com -- You received this message because you are subscribed to the Google Groups "American Vendor--IT Consulting" group. To unsubscribe from this group and stop receiving emails from it, send an email to sap-vendor+unsubscr...@googlegroups.com. To post to this group, send email to sap-vendor@googlegroups.com. Visit this group at https://groups.google.com/group/sap-vendor. For more options, visit https://groups.google.com/d/optout.
