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Resumes 341 - 350 of 25499 |
Coventry, RI
... support manufacturing when there are potential schedule changes Ensure any expiring material is disposed of in accordance with FDA guidelines SOP document author/owner utilizing CDOCs Special Projects: Worked with internal departments and an outside ...
- Feb 03
Waukesha, WI
... to develop innovative content strategies Final content review will align with Branding, Trademark, Registration and FDA requirements as well as Advertising and Promotional material review Directly contribute to $80M sales goal for GE service ...
- Feb 03
Reisterstown, MD
... Pharmaceutical & Tobacco Product Regulation (FDA CTP & CDER) ● Conducted expert analysis and strategic test plans for complex regulatory workflows, simplifying access to crucial information. ● Led design and front-end development (HTML/CSS) of ...
- Feb 03
Clarksburg, MD
... Adept at leading teams, maintaining compliance with HIPAA and FDA standards, and improving workflow efficiency. Demonstrated expertise in patient care, technical documentation, redaction, and quality assurance. Recognized for reliability, attention to ...
- Feb 02
Mansfield Center, MA, 02048
... • Work closely with our maintenance department to ensure proper repairs to the inside and outside of the building conforming to FDA Regulations. • Conduct performance reviews as well as corrective action documents when SOPs are not observed. • Work ...
- Feb 02
Walpole, MA
... unresolved issues • Review all AESIs SAEs to ensure that all necessary parties are notified • Training new staff • Assists with FDA audits Clinical Trial Associate Sep 2023 – January 2025 • Organizes study documents and materials • Create CRFs and ...
- Feb 02
Louisville, KY
... Event manager experience (10+ years) • Supervising experience • Change management • Renovation • Administrative experience • FDA regulations • Section 8 • Contract management in nursing • Healthcare risk management software • Resource allocation in ...
- Feb 02
Vuyyuru, Andhra Pradesh, India
... redesigned ASP.NET pages of USDA’s eDRS and ColdFusion pages of FDA’s Watering Point and EPA’s DWTS to be Section 503 compliant developed/deployed web-pages, stored-procedures, functions and SQL-scripts for USDA FAS (ASP.NET/SQL-Server-2008R2) and ...
- Feb 01
Bridgewater, NJ
Sarada Atluri New Jersey 908-***-**** ************@*******.*** Linkedin Professional Summary Accomplished pharmacovigilance publishing leader with extensive experience in global dossier management, electronic submissions, and compliance with FDA, ...
- Feb 01
Williams, AZ, 86046
... for individuals with Parkinson's disease • Management • Negotiation • Communication skills • Assisting with ADLs • Cooking • FDA regulations • Delivery driver experience (1 year) • Managing social services clients • End-of-life care • Oral hygiene ...
- Jan 31