|
Resume alert |
Resumes 61 - 70 of 234 |
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
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
Greenfield, IN, 46140
... collection, while making sure that all the customer service standards are being portrayed established and complied Followed FDA, AABB and HIPPA regulations to ensure the quality of the blood Trained as apheresis technician to comprehend and follow ...
- 2018 May 17
Indianapolis, IN
... Highly proficient in driving and ensuring all activities comply with ISO Standards, FDA regulations, current Good Manufacturing Practices (GMP’s), customer specifications, and all other applicable requirements. •Quality Management System •FDA, ISO & ...
- 2018 May 12
Indianapolis, IN
... viability assays: MTT, CCK8, SRB Microplate handling for high throughput screening for cell based assays Good working knowledge of ICH GCP principles and ICH compliant regulatory submissions - IND, NDA, BLA, GMP, ISO and FDA regulatory guidelines. ...
- 2018 Apr 26
Indianapolis, IN, 46241
... Strong knowledge of validations (IQ, OQ, PQ), DOE’s, GMPs, FDA, CAPA, and ISO 13485. EXPERIENCE: Medtronic (Minimally Invasive Therapies Group) Plainfield, IN Quality Engineer II November 2016 – Present Conduct periodic line audits to assess for ...
- 2018 Apr 09