| Resume alert | Resumes 41 - 50 of 81 |
Engineer Power Plant
Foxborough, MA
... Developed functional specifications, software test specifications (for FDA validation), Verification and Validation of the software including IQs, OQs, PQs, system configuration and Batch Unit Operations (i.e. Fermentation, reactor, centrifuge, ... - 2017 Sep 14
... Developed functional specifications, software test specifications (for FDA validation), Verification and Validation of the software including IQs, OQs, PQs, system configuration and Batch Unit Operations (i.e. Fermentation, reactor, centrifuge, ... - 2017 Sep 14
Human Resources Manager
North Attleborough, MA
... • Facilitated numerous performance and talent management workshops with all levels of the organization • Represented HR in all internal, inter-company, and external audits (FDA and ISO) • Facilitated corporate culture surveys; implemented programs ... - 2017 Apr 24
... • Facilitated numerous performance and talent management workshops with all levels of the organization • Represented HR in all internal, inter-company, and external audits (FDA and ISO) • Facilitated corporate culture surveys; implemented programs ... - 2017 Apr 24
Microsoft Office Computer Science
Bristol, RI, 02809
... oThe project also took into consideration the business aspect, FDA approval, intellectual property, and quality control. APPLICATIONS: Bioengineering Laboratory Work: oLab work included; the creation of a respiration measurement device using a ... - 2017 Apr 01
... oThe project also took into consideration the business aspect, FDA approval, intellectual property, and quality control. APPLICATIONS: Bioengineering Laboratory Work: oLab work included; the creation of a respiration measurement device using a ... - 2017 Apr 01
Manager Quality Assurance
Killingly, CT
... PROFESSIONAL EXPERIENCE Tower Laboratories, Ltd January 2008 to April 2016 Centerbrook, Ct Position: Compliance Manager Duties and Responsibilities: Ensure corporate compliance to FDA cGMP regulations in Drug, Medical Device and Dietary Supplement ... - 2016 Jul 10
... PROFESSIONAL EXPERIENCE Tower Laboratories, Ltd January 2008 to April 2016 Centerbrook, Ct Position: Compliance Manager Duties and Responsibilities: Ensure corporate compliance to FDA cGMP regulations in Drug, Medical Device and Dietary Supplement ... - 2016 Jul 10
Engineer Manager
Providence, RI
... Good leadership skills, technical skills, and FDA/Regulatory knowledge. MS Excel, Word, Power Point, and Outlook Bilingual (English-Spanish WORK EXPERIENCE American Wear Uniforms-East Orange, NJ 2015-Present Assistant Manager/Production Administered ... - 2015 Dec 20
... Good leadership skills, technical skills, and FDA/Regulatory knowledge. MS Excel, Word, Power Point, and Outlook Bilingual (English-Spanish WORK EXPERIENCE American Wear Uniforms-East Orange, NJ 2015-Present Assistant Manager/Production Administered ... - 2015 Dec 20
Technical Support Sales
Douglas, MA
... Have familiarity with Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) validation protocol for biotech, pharmaceutical and chemical industries for FDA’s Rule 21 CFR Part 11 compliance. TECHNICAL ... - 2015 Dec 10
... Have familiarity with Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) validation protocol for biotech, pharmaceutical and chemical industries for FDA’s Rule 21 CFR Part 11 compliance. TECHNICAL ... - 2015 Dec 10
Validation Engineer
Franklin, MA
Sita Dahal acso87@r.postjobfree.com SUMMARY Experience in Process Validation/Equipment Validation, Risk Management, Design of Experiments, Process Improvement and Quality Control in compliance with FDA regulations. Extensive validating experience in ... - 2015 Dec 05
Sita Dahal acso87@r.postjobfree.com SUMMARY Experience in Process Validation/Equipment Validation, Risk Management, Design of Experiments, Process Improvement and Quality Control in compliance with FDA regulations. Extensive validating experience in ... - 2015 Dec 05
Quality/Document/Project Coordinatior
Foxborough, MA, 02035
... • Laboratory Validation testing was written, organized and completed using the requirement documentation from the testing or equipment suppliers, on time and completed within company and FDA guidelines. • Daily Quality Control was processed on all ... - 2015 Oct 05
... • Laboratory Validation testing was written, organized and completed using the requirement documentation from the testing or equipment suppliers, on time and completed within company and FDA guidelines. • Daily Quality Control was processed on all ... - 2015 Oct 05
Senior Project Manager
Fall River, MA
... Participated in all ISO and FDA audits as it pertained to products within my responsibility. Senior company manager leading the development of medical devices. Single use sterile disposables. Managed multiple projects through “Phase Gate” ... - 2015 Jun 04
... Participated in all ISO and FDA audits as it pertained to products within my responsibility. Senior company manager leading the development of medical devices. Single use sterile disposables. Managed multiple projects through “Phase Gate” ... - 2015 Jun 04
SupplyChain - Procurement
Westport, MA
... • Knowledgeable with product quality standards with focus on GMP, FDA, arid ISO Standards • Successful supplier consolidation/management of Blanket Orders achieving significant cost-savings and improved overall supplier quality. Continuous ... - 2015 May 26
... • Knowledgeable with product quality standards with focus on GMP, FDA, arid ISO Standards • Successful supplier consolidation/management of Blanket Orders achieving significant cost-savings and improved overall supplier quality. Continuous ... - 2015 May 26