Wednesday, October 2, 2019

REQ: Validation Analyst with Trackwise

Mail Resumes to: vik@greymatterscorp.com  

Hi,

One of our Clients is looking for:

Validation Analyst with Trackwise

Duration: 12 Months
Location: Peapack, NJ

Details of the req:
• Experience with TrackWise 7/8/9.x versions, which is a product specific to Life Sciences industry.
• Good knowledge to Configure workflows to meet requirements
• Analyze requirements to recommend approaches for building and changing workflows
• Sparta Certification or equivalent (Good to have)
• Experience with Complaint Handling, CAPA, Audits, Deviations/Investigations implementation (At least two implementations)
• Good understanding of Regulatory Reporting, TrackWise Coordinator, TrackWise Migrator
• Trend and impact analysis to recommend remediation/improvements based on their implications on IT maintenance and business use.
• Experience with ITIL philosophy and SDLC methodologies.
• Strong knowledge on Oracle PL/ SQL.
• Good experience in developing TrackWise Web services and ability to connect with multiple third part systems such as SAP , LIMS , CRM systems
• Strong knowledge on Crystal Reports.
• Good knowledge on Java, J2EE technologies.
• Good knowledge of migrations from source systems to target (TrackWise ) based systems
• Good understanding of business concepts and experience as a developer in a regulated environment.
• Prior experience of working in a large scale support and maintenance environment.
• Excellent and matured communication skills required at client side and interpersonal skills.
• Understanding of Good Documentation Practice (GDP)
• Familiarity with Clinical, Pharma & Regulatory compliance domain would be a plus point.
• Ability to understand domain and provide value additions or improvements.

Please reply with resume in word format with Contact Details and Rates.

Regards,

VIK GARG 

GMT

vik@greymatterscorp.com   


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