| Resume alert | Resumes 121 - 130 of 460 |
Lab Technician Engineer
Haverhill, MA
... Participated in many facets of product development within a biomedical company by following standard operating procedures and work instructions controlled by an ISO/FDA-compliant quality management system. Established and maintained research goals ... - 2019 May 13
... Participated in many facets of product development within a biomedical company by following standard operating procedures and work instructions controlled by an ISO/FDA-compliant quality management system. Established and maintained research goals ... - 2019 May 13
Manager Engineering
Hudson, NH, 03051
... FDA cGMP ISO 300 people and remote field sites/repair depots. VP Operations Developed strategic operating plans, integrated and consolidated remote activities into the plants, drove cross functional teams to address customer issues in the quality, ... - 2019 Apr 19
... FDA cGMP ISO 300 people and remote field sites/repair depots. VP Operations Developed strategic operating plans, integrated and consolidated remote activities into the plants, drove cross functional teams to address customer issues in the quality, ... - 2019 Apr 19
Project Management
Boston, MA
... for different stages of production • Performed qualitative studies on product batch and ensuring compliance with GMP and FDA regulation Assistant Pharmacist Greater Kailash Hospital Indore, India Apr 2014– Aug 2014 • Implemented prompt stock ... - 2019 Apr 17
... for different stages of production • Performed qualitative studies on product batch and ensuring compliance with GMP and FDA regulation Assistant Pharmacist Greater Kailash Hospital Indore, India Apr 2014– Aug 2014 • Implemented prompt stock ... - 2019 Apr 17
Mechanical Engineer Medical Device
Westford, MA, 01886
Meng Cui Experience in FDA/ISO ***** regulated medical device development Core Competencies: Design for Manufacturing, Research and Development, Design Verification Mechanical Engineer Personal Info Education Address Dec. 2018 Northeastern ... - 2019 Apr 13
Meng Cui Experience in FDA/ISO ***** regulated medical device development Core Competencies: Design for Manufacturing, Research and Development, Design Verification Mechanical Engineer Personal Info Education Address Dec. 2018 Northeastern ... - 2019 Apr 13
Mechanical Engineer Manager
Boston, MA
... Karl Fischer, Scanning Electron Microscopy on processed API to ensure 100 % adherence to Food and Drug Administration (FDA) regulation Lafarge, Chhattisgarh, India August 2013 – August 2016 Deputy Manager/ Senior Mechanical Engineer Managed and ... - 2019 Apr 11
... Karl Fischer, Scanning Electron Microscopy on processed API to ensure 100 % adherence to Food and Drug Administration (FDA) regulation Lafarge, Chhattisgarh, India August 2013 – August 2016 Deputy Manager/ Senior Mechanical Engineer Managed and ... - 2019 Apr 11
Engineer Software
South Hamilton, MA
... became de-facto standard for FDA submissions • IAM – developed multiple tools and applications using Active Directory, Centrify & Sun IDM • PKI & DigSig – help develop Basic Assurance CA and DSig workflow applications and services Wellington ... - 2019 Apr 01
... became de-facto standard for FDA submissions • IAM – developed multiple tools and applications using Active Directory, Centrify & Sun IDM • PKI & DigSig – help develop Basic Assurance CA and DSig workflow applications and services Wellington ... - 2019 Apr 01
Customer Service Representative
Cambridge, MA
... ● cGMP, SOPs, Batch record, FDA regulations, Gowning, quality assurance, quality control ● Validation and calibration of equipment (autoclave, pipette man and pH meter) ● Cell culture & bacterial cell culture scale up, Upstream, Downstream process, ... - 2019 Mar 19
... ● cGMP, SOPs, Batch record, FDA regulations, Gowning, quality assurance, quality control ● Validation and calibration of equipment (autoclave, pipette man and pH meter) ● Cell culture & bacterial cell culture scale up, Upstream, Downstream process, ... - 2019 Mar 19
Mechanical Engineer
Boston, MA
... (WI, SOP, DHR, FMEA) to reflect the current design process using Good Manufacturing Practice documentation under a company FDA and ISO-conforming quality system Siemens Healthcare Diagnostics • Walpole, MA Mechanical Engineering CO-OP January 2009 ... - 2019 Mar 11
... (WI, SOP, DHR, FMEA) to reflect the current design process using Good Manufacturing Practice documentation under a company FDA and ISO-conforming quality system Siemens Healthcare Diagnostics • Walpole, MA Mechanical Engineering CO-OP January 2009 ... - 2019 Mar 11
Lab Scientist
Danvers, MA
... Siemens Healthineers, Walpole, MA— QC Technician March 2018 - October 2018 Performing QC testing and documentation in accordance with FDA regulations for GMP for medical devices and equipment. EDUCATION Salem State University, Salem, MA — Bachelor ... - 2019 Feb 26
... Siemens Healthineers, Walpole, MA— QC Technician March 2018 - October 2018 Performing QC testing and documentation in accordance with FDA regulations for GMP for medical devices and equipment. EDUCATION Salem State University, Salem, MA — Bachelor ... - 2019 Feb 26
Manager Sales
Waltham, MA
... ECR standards implementation and compliance Production Planning Handled quality systems implementation and maintenance-ISO, FDA, GMP, GDP Project Management Facilitated and support of Kaizen events Process Optimization Production management and ... - 2019 Jan 17
... ECR standards implementation and compliance Production Planning Handled quality systems implementation and maintenance-ISO, FDA, GMP, GDP Project Management Facilitated and support of Kaizen events Process Optimization Production management and ... - 2019 Jan 17