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Resume alert |
Resumes 31 - 40 of 574 |
Newtown, PA
... VP, National Accounts, Eurand Pharmaceuticals, Milan, Italy/Yardley, PA 4/2009 - 5/2011 Responsible for a start-up company, with the launch of FDA approved products into the US. Sales from $0 to $145M first year, Exceeding fist year expectations by ...
- 2023 Dec 03
Mount Laurel, NJ, 08054
Lamont Michael Fulton Regulatory Affairs Consultant Former FDA Reviewer and Policy Analyst Reviewed hundreds of Drug Applications submitted to the FDA for market approval in the United States. Served as adviser to the Office of Regulatory Affairs to ...
- 2023 Nov 29
Fairless Hills, PA
... by 15% and healthcare membership initiatives by 9% Conducted market research & identified solutions to challenges faced by FDA regulations for external stakeholders SENIOR REGIONAL MARKETING MANAGER, 2008 to 2012 DOW JONES & COMPANY, South ...
- 2023 Nov 29
Dayton, NJ
... • Planned Equipment & Time Constraints • Performance Reporting & Updates • International Regulations & Customs • Import/Export & FDA/DEA Experience • Proactive & Responsive Customer Service • Excellent Verbal & Written Communication Work Experience ...
- 2023 Nov 27
Freehold, NJ
... Design Assembly Automation Pro-e Cad Design Fixturing and Tooling Die Casting CNC Machining – 4th and 5th Axis CNC Programing FDA ISO OSHA Regulatory Compliance EXPERIENCE 10/2021- present Caes Inc Manufacturing Engineer Kaizen events, Cell design, ...
- 2023 Nov 23
Hillsborough, NJ
... Department • 2 years of GMP quality compliance/quality assurance experience • Extensive knowledge of GAMP 5, ICH Guidance, FDA regulations including CSA (draft), EU Annex, MHRA, and OECD Guidelines, FDA’s Pre-Approval Inspection (PAI) Program • ...
- 2023 Nov 17
Somerset, NJ
... Broad knowledge of Environmental monitoring, microbiology, Regulatory submissions including IND, ANDA and NDA, Annual Product Review, Process Validation: GxP, cGMP, cGLP, cGCP, GDP, FDA, ANVISA and MHRA regulations, DEA, EMA, USP, EP and ICH ...
- 2023 Nov 16
Medford, NJ
... Reviews/Edits/Approvals of Clinical Research Protocols for Medical Researchers IRBs, IACUC, Biosafety Protocols Management and Knowledge of EPIC, CITI, ICMJE, USDA and FDA Regulations Build Cross-Functional Collaborations between Academic, Biotech ...
- 2023 Nov 14
Princeton, NJ, 08544
... •Knowledge in ICH, FDA, and EU guidelines. •Excellent written and interpersonal communication skills with international conference presentations and peer-reviewed journal publications. •Recipient of GOLD MEDAL, Meritorious Student Award, Doctoral ...
- 2023 Nov 13
Monmouth Junction, NJ
... Successfully navigated FDA audits and facilitated regulatory submissions. • Proficient in batch record review and release, APQR, Stability and Retain Sample Management, and handling of Product Complaints. • Highly process-oriented approach to ...
- 2023 Nov 10