Rancho Santa Margarita, CA
... 2014) North American Science Associates (NAMSA) 9 Morgan Irvine CA 92618 Responsible for ensuring policies, procedures and requirements are followed in accordance with ISO 13485 / FDA GLP requirements / 21 CFR related to medical device testing for ...
- May 08
San Jose, CA
... and Improvement ● Supply Chain Management ● Quality Control ● Interviewing and Prescreening ● GMP ● CSF/Quarterly goals ● FDA Audit ● ERT Member/CRP Certified ● PCB Assembly/Soldering/Mil Spec, ● Voyager ● Jira ● AI ● Managed logistics for offsite ...
- May 08
Charles Town, WV
... Physiology UC Irvine, CA Recent Training & Industry Related Courses Change Control Management, Principles of Auditing, FDA Tour, FDA QSR/ISO 13485:2016 – QMS For Medical Devices, Lifecycle Approach to Cleaning and Process Validation, Conference ...
- May 08
Belvidere, NJ, 07823
... able to meet multiple tight deadlines In-depth understanding of routing and production processes, OPDP guidelines, and FDA advertising regulations for fair balance, safety information, and branding placement Expert user of PowerPoint, Word, and ...
- May 08
Arvada, CO
... Signature (ERES), Annex 11 •Worked across various platforms and with multiple internal and external business partners to implement Corrective Action Plans (CAPA) •Prepared documentation for onsite Food and Drug Administration (FDA) audits. ...
- May 08
El Paso, TX
... after the evaluation of Import Restrictions such as: consumption, antidumping, TIB's, warehouse entries, quotas, OGA's (FDA, USDA, FCC, DOT, HAZMAT) • FDA Data updates • PGA data • Harmonized Tariff Schedule • Successfully validated Harmonized ...
- May 08
Elgin, TX, 78621
... EE, ME to meet performance requirements ·Preparing cost estimates for various assemblies or single parts ·Familiarity with FAA and FDA requirements ·Preparing technical publications and CMMs to accompany designs ·Creating procedures, reports, and ...
- May 07
Alpharetta, GA
... with improving the risk management and complaint processes ● Stretching expertise to assist regulated division to prepare for FDA inspection O&M Halyard 04/17-08/22 Technical Quality Leader ● Development of the Risk Management files which includes ...
- May 07
Chicago, IL
CONTACT: Homewood, IL ad5jor@r.postjobfree.com 815-***-**** www.linkedin.com/in/richard- santoro-cssbb-tqmp-2346593 SPECIALTIES: Quality Management System & Compliance FDA GMP Medical Device & Pharmaceutical Regulations EU MDR, Health Canada SOR/98 ...
- May 07
White Bear Lake, MN
... Well-versed in varied commercial transactions, USDA and FDA regulatory compliance, IRS collections, bankruptcy, foreclosures, mediation, intellectual property, licensing, probate, trusts and estate planning, guardianships and conservatorships, state ...
- May 07