[20525MSCRMCV] Pilgrim Software in Northridge , CA

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Pilgrim Software

Work Location: Northridge , CA

Experience with Pilgrim Software, which is a product specific to Life Sciences Quality industry.

Good knowledge to configure the Pilgrim system to meet requirements of the customer including report writing

Experience with Complaint Handling, CAPA, Audits, Deviations/Investigations implementation (At least two implementations)

Qualifications Basic

• Bachelor's degree or foreign equivalent from an accredited institution or three years of progressive experience in the specialty in lieu of every year of education.
  
• At least 8+ years in Information Technology / LifeSciences field. 

Technical Skills

• Experience with Pilgrim Software, which is a product specific to Life Sciences Quality industry.
  
• Good knowledge to configure the Pilgrim system to meet requirements of the customer including report writing
  
• Act as the focal point for project communications to ensure success of the project
  
• Analyze requirements to recommend approaches for building quality business processes using Pilgrim tool 
  
• Provide consulting services to the assigned projects as required including product technical consulting, integration/migration strategy, business process re-engineering, engineering analysis, customization requirements, product installation, data conversion requirements, product validation and custom report analysis
  
• Experience with Complaint Handling, CAPA, Audits, Deviations/Investigations implementation (At least two implementations)
  
• 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.
  
• 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) including ISO 9000, cGMP and FDA Regulations
  
• Familiarity with Clinical, Pharma & Regulatory compliance domain would be a plus point.
  
• Ability to understand domain and provide value additions or improvements.

Roles and responsibilities

• Work with business users to understand the issues and business processes
  
• Address technical issues whenever required.
  
• Review and test the deliverables before handing to clients.
  
• Provide regular updates to the customer on the ongoing work.
  
• Provide technical solutions to the problems/enhancements.
  
• Client management and coordination with various stakeholder teams in the project

Regards,

Jeni Tailor

Talent Acquisition Specialist

Gemini Consulting and services

314-272-3141

jenitailor@gemini-us.com 

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