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Resumes 351 - 360 of 25476 |
North Augusta, SC
... Familiar with HTS, Customs, OGA, FDA and ATF Clearance Regulations Used judgment and independent initiative needed to find, adapt, and apply approaches to solve problems. 08/2013-11/2014 Remote Titlemax Auto Loan Processor and SC and GA Title Clerk ...
- 2025 Sep 12
Philadelphia, PA
... Quality Engineer Consultant LANSDOWNE, US 19050 * *********@*****.*** * 702-***-**** Pharmaceutical/Medical Device Quality Control/Quality Engineer Consultant with years of experience in ensuring compliance with FDA regulations and GMP standards. ...
- 2025 Sep 12
Hagerstown, MD
... - Layoffs Supported Teksouth in the closure of sole-source contracts for the implementation of EntelliFusion, a BI software analytics platform, across multiple federal agencies including GSA, USDA, Forest Service, FDA, NOAA, DOE, FBI, and DOT. ...
- 2025 Sep 11
Kansas City, MO
... quality/regulatory (FDA, DEA, MHRA)
- 2025 Sep 11
Indianapolis, IN
... Python and Java SQL database experience in Oracle and PostgreSQL SDLC environments: Agile, SCRUM, and Waterfall 21 CFR Part 820, FDA Part 11 PEGA TECHNICAL CERTIFICATIONS: PEGA Certified: Senior Software Architect (CSSA, 7.4) PEGA Certified: System ...
- 2025 Sep 11
Rockville, MD
... Rockville, MD, First Impression Coordinator ● Giant Food, Germantown, MD, Seafood and Meat Assistant ● Zimmerman Associates/FDA, Silver Spring, MD, Record Technician ● Logistic Applications/DOE, Germantown, MD, Property Supply Clerk/Administrative ...
- 2025 Sep 11
Lawrenceville, GA
... Data Engineer May 2024 - May 2025 Go Audits Delaware, USA • Migrated 22 legacy SAS pipelines into Databricks Delta Lake with incremental MERGE logic, processing 12TB/day and reducing FDA reporting timelines from 14 days to 72 hours. • Streamlined ...
- 2025 Sep 11
Coatesville, PA
... Highlights: Advised business partners on contractual terms and conditions in order to reach acceptable language Established processes for approvals and other internal audit and FDA compliance requirements PA HOUSE LEGISLATIVE POLICY & RESEARCH ...
- 2025 Sep 11
Newark, DE
... CitiusTech, India May 2022 – Jul 2023 Java Full Stack Developer Designed modular clinical workflows with Java 21 and SOLID principles, enabling reusable components for SaMD features and accelerating FDA-compliant module development. Built dynamic ...
- 2025 Sep 11
Pune, Maharashtra, India
... ● Implemented UDI attributes (FDA product codes, submission numbers, marketing authorization types) and automated UDICO submission workflows to meet medical device regulatory requirements with validation and error-handling logs to achieve 100% FDA ...
- 2025 Sep 11