FDA Resumes

Hyderabad, Telangana, India
... GxP, CSV & Regulatory Compliance: Validation, change control, and lifecycle management of IT systems aligned with GMP, GLP, 21 CFR Part 11, FDA, WHO, MHRA, DCGI, and data integrity expectations. Audit & Inspection Readiness: Hands-on experience ... - Apr 13

Calhoun, GA
... Compliance with FDA, AABB, and Joint Commission in chemistry and blood bank Erica Kennedy 278 Dogwood Lane SE Calhoun, GA 30701 678-***-**** ****************@*****.*** HAMILTON MEDICAL CENTER- DALTON, GA Medical Laboratory Technician, Mar. ... - Apr 13

Muscat, Muscat Governorate, Oman
... procedures and methodologies Root Cause Analysis (RCA) Auditing (internal and external) Regulatory compliance (GSO, SFDA, FDA, USDA, EU, CFIA, etc.) Food microbiology and food chemistry Crisis management and Recall Supplier Quality Management New ... - Apr 13

Hawthorne, CA
... shipments,,delays, expedite shipments Certified in Time Management, Critical thinking, problem solving skills Air, Ground, Ocean Fed Ex, UPS, Hazmat, DG, TSA, Customs, FDA, USDA, Customs Excel, MS Office Cargowise, AS400, Maestro, SAP, Tableau. ... - Apr 12

Leominster, MA
... Boston, MA • Directed clinical trial logistics, packaging design, and CMO coordination for FDA submission. • Oversaw global product export operations, ensuring timely and compliant delivery. • Created technical documentation, including instructions ... - Apr 12

Ashburn, VA
... Sales Food safety management Customer inquiry handling Maintenance Account management Accounts receivable Retail sales FDA regulations iOS Cutting Order Picking Working with high schoolers Order picker Reach truck Sales administration Store ... - Apr 12

Nargund, Karnataka, India
... Submission of reports regarding the FFFI ( Fixed Fire Fighting Installations ) and FDA ( Fire Detection Alarm System ) to various department HOD’s. Providing service like De-Watering in case of emergency situation to any departmental requirements. ... - Apr 12

Mississauga, ON, Canada
... • Hands-on experience in the execution of production protocols, GMPs-FDA part 11, HACCP, Quality ISO- 9001, environment 14001 procedures, ISO/IEC 17025 standard and ISO 13485 (medical device license) • Hired, improved, and attentively trained ... - Apr 11

Lugoff, SC, 29078
... 1995-1997 Clinical Development Pfizer Inc., Groton, CT Organized and assembled applications for new medications to be submitted to FDA for approval. Team member for checks and balances system instituted for verification of completeness and ... - Apr 10

Dayton, NJ
... Experienced in tablet manufacturing processes including blending, granulaƟon, compression, and coaƟng, along with strict adherence to cGMP, SOPs, and FDA regulaƟons. Proven ability to maintain accurate documentaƟon, support audits, and collaborate ... - Apr 10