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Resumes 191 - 200 of 25488 |
Miami, FL
... Dedicated team player who thrives in fast-paced, high-volume environments, ensuring compliance with FDA regulations, GMP standards, and company policies. Education & Certifications Glass Making Certificate – Walter M. Wallack School Electrician ...
- Jun 27
Cary, NC
... Experience in supporting FDA submission related activities like converting SDTM & ADaM datasets into .xpt files, generating define.xml, and creation of Ad-hoc reports. Generated HTML, PDF and RTF reports using SAS Output Delivery System (ODS). ...
- Jun 27
Clairton, PA
... Technician product verification essentials, Pharmacy practices, Medical and pharmaceutical terminology, Prescription filling, FDA drug guidelines, Basic anatomy, Retail pharmacy procedures, Billing and Reimbursement, Medication Therapy Management, ...
- Jun 27
Superior, CO
... Adept at optimizing trial design, ensuring compliance with FDA, EMA, and ICH guidelines, and securing stakeholder buy-in for high-impact drug development initiatives. Skilled in scientific communication, market access strategy, and KOL engagement to ...
- Jun 27
Castalia, NC, 27816
... ● Keep procedure manuals in compliance with the requirements of various accrediting agencies, such as the FDA, JCAHO, etc. ● ● English Language ● Clerical ● Meditech ● Mosaic ● Athena ● Microsoft ● Excel ● ● Phlebotomy techniques ● Patient care ● ...
- Jun 27
Raleigh, NC
Alban Fergusson Knightdale, NC ***** 347-***-**** ***************@*****.*** SKILLS/QUALIFICATIONS • Strong knowledge of GMP (Good Manufacturing Practices), SOP, FDA regulations, EHS standards • Proficient in troubleshooting and repairing complex ...
- Jun 27
Atlanta, GA
... for clearance of goods into the United States • • Ensures compliance regarding U.S Government regulatory agencies such as FDA, EPA, FCC, Fish & Wildlife, etc • • Handles accounting processes accurately and in a timely manner Coordinate shipments ...
- Jun 27
Hackensack, NJ
... Vast working knowledge of FDA, Quality System Regulations, ISO 9001/ISO 13485, CE marking requirements and current, Medical Device Directive, FMEA and risk analysis, validation/verification, design input, output, and reviews, Subcontractor auditing ...
- Jun 27
San Diego, CA
... ● Roles include Quality, Quality Document Control,Biotechnology Lab Roles, Analytical Chemistry, Liquid Chromatography ( HPLC ), Toxicology Synthetic testing, MRB Inventory Coordinator,, and Logistics, FDA labelling, all positions compiled in a ...
- Jun 27
Washington, DC
... FDA Focus) (CITI Program, Online) (Aug. 06, 2024) Research With Minors - BIOMED (CITI Program, Online) (Aug. 06, 2024) FDA-Regulated Research (CITI Program, Online) (Aug. 05, 2024) The Professional Medical Interpreter® (Academy of Interpretation, ...
- Jun 27