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Indianapolis, IN
... Auditing Pharmaceuticals FDA Compliance Scanning Electron Microscopy Method Developments, Transfers Supervisory Skills Statistical Analyses (Excel, JMP) Small/Large Molecule developing CAREER HIGHLIGHTS Oxford Global Consulting Division for ...
- 2019 Feb 25
Fishers, IN
... are electronic listings of individual observations for a subject that comprise the essential data reported from a clinical trial, are one of four types of data currently submitted to the FDA along with patient profiles, listings, and analysis files. ...
- 2018 Dec 20
Carmel, IN, 46032
... She also completed required training modules (FDA and client mandated) and internal staffing firm courses on topics such as GMP, commissioning, validation, writing, execution, automation, safety, and project management. Some of her project ...
- 2018 Oct 27
Pittsboro, IN
R&D ENGINEER/TECHNICIAN Develop Prototypes, Manage Research Laboratories, and Support Production Extensive experience working at an FDA-regulated medical device manufacturing company. Effectively write reports and manage records for quality ...
- 2018 Oct 27
Indianapolis, IN
... study (FDA regulated) ●Fetal rhesus lung cells tissue culture and inoculation of live virus ●Outstanding soldier award from commanding general ●Fast track early promotion recipient Computer Skills Began studying computer programming at age 11. ...
- 2018 Sep 20
Fishers, IN, 46038
... Engrg – Program Manager, Project Engineer, Product Designer March 1993 – present ZIMMER-BIOMET – Post Market Quality Engineer, FDA 21 CFR Part 820 Mar 2017 to present HILL-ROM – Post Market Quality Engineer, FDA 21 CFR Part 820 April 2014 – Nov 2016 ...
- 2018 Aug 01
Indianapolis, IN
... Complied at all times with SOX, USDA, FDA, DOT and U.S. Customs guidelines and regulations. Loaded and unloaded ship cargo. Used item numbers to properly stock warehouse. Recorded numbers of units handled and moved using daily production sheets and ...
- 2018 Jun 13
Indianapolis, IN
... Procedures had to meet new standards within FDA and Lilly validation guidelines. Updates of validated documents and procedures to meet FDA and Lilly validation guidelines. Creation of scripts and custom documents to validate, document, enhance, ...
- 2018 Jun 04
Brownsburg, IN, 46112
... Project/Primavera Project Management Body of Knowledge, PMBOK Compliance Regulatory Multi-Industry Experience, DOD, DOE, EPA, FDA, Life Science, Financial/Accounting SEI Software Engineering Institute, CMM Maturity Model, Software Development ...
- 2018 May 28
Indianapolis, IN
... My in-depth knowledge, experience and expertise are: ISO 9000, 9001:2008, ISO 14001OHSAS 18001, GMP, FDA work environment Quality processes and statistical techniques / SPC, Audit and inspection Root Cause Analysis, Manufacturing Investigation and ...
- 2018 May 25