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Resumes 71 - 80 of 245 |
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
Indianapolis, IN
... Navigated application of oPP programs to ensure compliance with FDA FSMA regulations as well as update all HACCP plans to reflect all new changes. Overall plant improvement in internal audit performance through root cause analysis, tracking of open ...
- 2018 Mar 22
Indianapolis, IN
... field agents, in compliance with FDA requirements. prevent them from accessing the therapies they need while serve as a primary contact for representatives and stakeholders from pharmaceutical companies involved in monitoring and understanding ...
- 2018 Mar 05
Noblesville, IN
... supplies to comply w/FDA and GHA. - Partnered with corporate A/P for consolidation of invoices and automated bill payment via the internet. - Successfully negotiated contracts with 3rd party and LTL carriers to reduce transportation costs by 42%. ...
- 2018 Feb 12
Indianapolis, IN
... Ability to audit and investigate processes, and operate and/or troubleshoot analytical equipment in a medical device and pharma facility under FDA QSR 21 CFR Part 820 and ISO13485 standards. Acquired Skills Master’s Degree People/Team Leadership ...
- 2018 Jan 22
Zionsville, IN, 46077
... Quality Assurance/Quality Control Management, FDA/USDA, SQF, BRC HARPC Preventative Control, HACCP, Quality Systems and R&D SUMMARY; Have more than 10 years of knowledgeable experience in the Food industry in conducting experiments, producing sample ...
- 2018 Jan 04
Indianapolis, IN
... All Health Imaging products were designed and manufactured to be FDA compliant. Key Achievements: Implemented lean and/or six sigma manufacturing strategy throughout all sites making significant product flow, cost and quality improvements. Directed ...
- 2017 Dec 13