chintal mehta
- 21 cfr part 11
- glp
- quality assurance
- 14+
Overview
Business professional with successful track record of managing Dossiers, document management and other regulatory documents according to agency requirements. System expert for the electronic document management and publishing for regulatory documentations (Documentum & CoreDossier); Experienced in computer validation (OQ, PQ) and troubleshooting; Lead and provide global report coordination teams on process harmonization and improvements; Expertise in: Process improvement, Business relationships, Regulatory document management, Quality and compliance, GLPs, SOPs, FDA regulations, including CFR part 11, Project management, Training, various software such as Documentum, CoreDossier, Adobe Acrobat with ISI toolbox, MS office
Explore their background, skills, and professional experience in pharmaceuticals.
Contact Information
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Skills & Expertise
Professional Information
customer_service
Working at sanofi in the pharmaceuticals industry. Based in united states.
pharmaceuticals
Specialized experience and expertise in pharmaceuticals sector with proven track record.
support
Focused expertise in support with comprehensive experience.
Experience
sanofi
senior manager, quality projects and support, r and d us sqo
Languages
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