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Resume alert |
Resumes 11 - 20 of 309 |
Seaside Park, NJ
... • Remained vigilant to industry trends and FDA mandates, ensuring my designs captivated and effectively conveyed the safety, efficacy, and credibility of BMS offerings. Art Director Robert Greenberg and Associates, 1998-2001 • Crafted compelling ...
- Jan 29
New Brunswick, NJ, 08989
... external studies supporting risk mitigation strategies Led global efforts in automation of data capture and Robust Study Design for In Vivo Studies Provided post-marketing support to FDA queries on older small molecules as well as the HIV portfolio. ...
- Jan 22
Brick, NJ, 08724
... 01/1999 to 01/2002 • Manage pharmaceutical accounts • Organized and distributed all literature and promotional materials for sales reps • Accountability for representative samples, distribution forms to be compliant with the PDMA and the FDA. ...
- Jan 18
Plainsboro Center, NJ, 08536
... skills Courteous demeanor Adaptive team player Energetic work attitude Opening/closing procedures Staff Development FDA Compliance Problem-Solving Skills Regulatory Compliance Quality Assurance and Control Patient Education and Counseling ...
- Jan 17
Lakewood, NJ, 08701
... Maintain, troubleshoot, test, and calibrate all Facility AND Building equipment and computers to FDA, I.S.O. standards and maintain records. Certificates and calibration reports of all work. This includes computers and ancillary and specialized ...
- Jan 09
East Windsor, NJ
... Strong knowledge about Pharmaceutical/Medical device regulations like FDA: 21 CFR Part 210, 21 CFR Part 211 and 21 CFR Part 820 and involved in implementation of CFR Part 11 rules (Electronic Records, Electronic Signatures, Audit Trails, and ...
- Jan 06
Keyport, NJ
... Central Storage Picked orders and served as a Receiving Clerk EDUCATION High School Graduate RELATED TRAINING FDA Good Manufacturing Practice Powered Industrial Lift Truck Training OSHA related training CERTIFICATIONS Certified Forklift Operator ...
- Jan 03
Monroe Township, NJ, 08831
... • Creation and validation of E-submission requirements to the FDA which involved – creating annotated CRF, SAS transport files (XPT files), SDTM and ADaM, Define.xml documents, Reviewer’s guide etc. • Having achieved excellent organizational and ...
- 2023 Dec 06
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