Why this role stands out
Step into a high-impact role at KRG Technology Inc., where you will leverage your expertise in Pharma IT and GxP standards to lead critical projects within the dynamic life sciences sector. This position is perfect for a seasoned professional with PMP certification who thrives on driving complex regulatory submissions and fostering collaborative team environments. Apply today to advance your career at a reputable firm that values your specialized technical skills and commitment to excellence.
Quick overview
Job description
Mandatory Skills: Pharma IT, GxP Project, PMP Certification
Domain Experience
• Working knowledge of ICH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs.
• Broad knowledge of drug development process and client needs
• Prior experience working on regulatory submissions
• Familiar with 21 CFR part 11, GXP and other Life Sciences regulations
Technical Experience
• Experience with LIQUENT Insight publisher, Veeva platform strongly preferred; however, consideration will be giving to candidates with experience with other electronic publishing systems
• Experience with Waterfall and Agile development
• Thorough understanding of Software Development Life Cycle (SDLC) and all related documentation
All your information will be kept confidential according to EEO guidelines.
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