вторник, 3 сентября 2013 г.

Compliance Analyst at Raritan

Job Description

Computer System Validation - Agile methodology for FDA-regulated applications.

Period: 09/23/2013 to 03/28/2014
Title: Computer System Validation
Location: RARITAN / NJ / 08869

Description
Requires substantial experience with SDLC (System Development Life Cycles) using Agile methodology for FDA-regulated applications.
Must be experienced in developing Computer System Validation deliverables for FDA-regulated applications:
Validation Plans, Requirement Specifications, various levels of software testing scripts (IQ, OQ, PQ), Traceability Matrix, and Validation Reports.
Requires thorough knowledge of US CFR 21 Part 11 regulations.
Requires working knowledge of at least one of the following: US CFR 200 or 300 or 800 series.
Experienced with high volume application testing environment.
Requires technical competence with n-tier application development and cloud-hosted applications.
Experience with automated Software Testing tools is a plus. Familiarity with QA Auditing is a plus.
Familiarity with a Corrective and Preventative Action program is a plus. Experience with medical device validation/qualification is a big plus.

Non-Technical:
Experienced in working within an FDA regulated environment for the Pharmaceutical and/or Medical Device industries.
Ability to work within an agile project team setting.
Ability to work in a rapid deployment group.
Ability to self-direct and follow up with all compliance team members to ensure timely deliverable of project documentation.
Jointly develop, communicates plan with project team.
Insure timely flow of information with project team.
Manage validation Project Plan.
Responsible for tracking, coordination, and project planning of Computer System Validation activities.

Methodology/Certification: Bachelor Degree in Chemistry, Mathematics, Engineering or Computer Science.
Advanced course work in technical systems or continued education in technical disciplines is a plus.

Experience: 5-7 years Pharmaceutical and/or Medical Device industries validation, 2-3 years SDLC#CBRose#



Rose International is an Equal Employment Opportunity Employer-M/F/D/V

About Rose
  • Founded in 1993
  • 21 office locations across the U.S.
  • 130+ Customers; corporations and government agencies
  • Employee Oriented Company
  • Challenging Assignments across the U.S.
  • Continuous Professional Development
  • Challenging, Exciting and Professional Atmosphere

Join Our Team Today!

Employee Comments

We want you to work with us, but dont take our word for it. Take a look at this sampling of employee comments. They speak for themselves.
Each time I contacted Rose, I was completely satisfied with the great attention and customer service I received. Each person was extremely knowledgeable and patient with my concerns or questions. Diana, Consultant
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Job Requirements

 
Country: USA, State: New Jersey, City: Raritan, Company: Rose International.

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