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Resume alert |
Resumes 11 - 20 of 249 |
Groton, MA
... Six Sigma, APICS, PMP, Lean Manufacturing, Kaizen, ISO, Trade Compliance, 5S, Train the Trainer, JIT, TQM, VOC, Prince II, PDCA/SDCA, DMAIC, CMMI, ITAR, FAR, NISPOM, SOX, FDA/MDD/MDHR, 7 & 9 Step Problem Resolution, cGMP, GCP, GDP, EU MDR, APAC, FAT ...
- Jan 15
Pepperell, MA
... Six Sigma, APICS, PMP, Lean Manufacturing, Kaizen, ISO, 5S, Train the Trainer, JIT, TQM, VOC, Prince II, PDCA/SDCA, DMAIC, CMMI, ITAR, FAR, NISPOM, SOX, FDA/MDD/MDHR, 7 & 9 Step Problem Resolution, cGMP, GCP, GDP, EU MDR, APAC, FAT, UAT, SIT, AUT A ...
- 2023 Dec 22
Framingham, MA
... React, Node, MVC.NET, MS SQL, NoSQL, MySQL, AWS technologies, EC2, Load Balancing, Jira, Confluence, Git, P4 07/15 - 5/16 SANOFI, CAMBRIDGE, MA PRINCIPAL APPLICATION DEVELOPER (B2C) ● Architected first FDA approved insulin dosing mobile app. ...
- 2023 Dec 19
Woonsocket, RI
... I have worked with auditing bodies such as AIB, SQF, BRC, and FDA. I am trained in HACCP (certified), FSMA, and food safety programs. I am driven by the challenge of developing people and processes to exceed expectations. Achieving goals and KPI’s ...
- 2023 Nov 12
Newton, MA
... -Led compounding pharmacy operations, ensuring strict cGMP, FDA, and DEA compliance. -Successfully guided FDA audits, showcasing strong regulatory adherence. -Established a culture of compliance and proactive risk management. -Optimized ...
- 2023 Oct 12
Worcester, MA
... Following WSDP and remaining compliant with Quality Assurance, FDA, and participating in customer Audits, ●Computer System Validation/cGMP, setting up brand new UPLC, HPLC, GC systems and instruments. Validating the IQ/OQ/PQ of various systems when ...
- 2023 Oct 10
Needham, MA
... Analyzed, maintained, and go over test documents to meet 21 CFR 820 (FDA QSR) and ISO requirements. Manually generated and implemented templates for Test plan, Test Cases, and Test Scripts and performed Testing on the entire application. Worked ...
- 2023 Oct 03
Belmont, MA
... For pharmaceutical companies I review the FDA calendar and read industry publications to identify investment candidates. I analyze Phase I, II, III studies to examine the efficacy of the drug and assess the likelihood of FDA approval. I review ...
- 2023 Oct 02
Grafton, MA, 01519
... Faced regulatory audits with agencies like US-FDA, WHO and FDA-Thailand. Core competencies Ability to maintain lab with minimal supervision, attention to detail and handle pressure during high priority projects with effective stakeholder management ...
- 2023 Sep 18
Medway, MA, 02053
... - Weymouth, MA 2012 to 2014 Inspection and clean to FDA regulations of machinery before and after any runs ! Pump up a liquid to top of tank which then gets pushed through a nozzle to make a very fine spray which on the way down would contact ...
- 2023 Sep 17