IT - Technology Analyst | Life Sciences | Regulatory ...

Job Title: Technology Analyst | Life Sciences | Regulatory Systems Work Location: Parsippany, NJ 7054 Vendor Rate: XXX/hr Contract duration: 6months Target Start Date: 09 Feb 2026 Job Details: Must Have Skills Previous experience with SDLC and GLPGCP validation. Technical Writing or Documentation experience in a regulated industry Experience in Pharma or Pharma R&D Nice to have skills Technical Writing Experience in Pharma or Pharma R&D Detailed Job Description The Document Support Specialist supports projects across all areas of research and development. The individuals selected will have attention to detail, a positive attitude, a strong work ethic, be a self starter, and have the ability to manage multiple priorities. Job Requirements Develop and write documentation as part of SDLC software release and or validation projects. Documents such as project plans, requirements documents, validation related scripts matrices, migration plans, and design and c Minimum years of experience 5-8 years Top 3 responsibilities you would expect the Subcon to shoulder and execute Individual contributor As Individual contributor

Created: 2026-03-04