Duration: 6+ months to hire
Location : NY
Rate      : $ 40/ hr salary would be 60K +




Job Description:                This position is will convert in Q2, as a full
time hire.
Summary:
This position is responsible for providing IT support for validation
initiatives across Acorda departments. Lead initiatives as Business
Owner for validation of IT systems. Develop, implement, and maintain
IT SOPs in accordance with the Acorda Quality Management System.
Interface with Acorda Quality Unit to ensure compliance.



Essential Duties and Responsibilities:

.Assess systems to determine 21CFR11 and/or Sarbanes Oxley compliance
as well as writing test scripts, validation documents, and validation
reports.

.Provide training to new and existing Acorda employees regarding IT
policies and procedures.

.Collaborate with user groups to identify enhancements required for
existing systems.

.Coordinate the availability, capabilities and potential benefits of
both new and old systems through Email announcements, meetings, and
events (such as lunch n learn or open house) to increase awareness of
the document management system.

.Perform special IT projects and contribute to department business
needs.

Education and Experience:
B.S. in Computer Science or related degree with five years IT
experience within the regulated Pharmaceutical/Biotechnology industry.
Two-three years experience in providing IT validation and compliance
support to business owners and IT department management.
Computer Skills:
.Experience using QUMAS DocCompliance document management system.
.Proficiency with Microsoft Windows operating systems and Office
application suite.

Send resume: [email protected] or call 214-432-0218

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