| Resume alert | Resumes 11 - 20 of 377 |
Quality Assurance Medical Device
Downtown San Jose, CA, 95113
... Oct) · All associates are involved in every stage of molecular diagnotics · Followed good documentaion practice and procedure, GMP, SOP, compliance · Setup, trained, monitored, coordinated and operated manufacturing machine equipments · In-process ... - Mar 20
... Oct) · All associates are involved in every stage of molecular diagnotics · Followed good documentaion practice and procedure, GMP, SOP, compliance · Setup, trained, monitored, coordinated and operated manufacturing machine equipments · In-process ... - Mar 20
Medical Device Lean Manufacturing
San Jose, CA
... •Responsible for in-process product testing (pH, Conductivity, TOC & TA Testing) and product qualification during production processing, utilizing unique skills in aseptic technique, state-of-the-art cleanroom practices (as needed) DEA, FDA and GMP. ... - Mar 19
... •Responsible for in-process product testing (pH, Conductivity, TOC & TA Testing) and product qualification during production processing, utilizing unique skills in aseptic technique, state-of-the-art cleanroom practices (as needed) DEA, FDA and GMP. ... - Mar 19
Scrum Master Program Manager
Redwood City, CA
... Ensured all deployments follow established processes to ensure quality, repeatability, efficiency and GMP/SOX compliance so customers are minimally impacted by changes in production. (Validated and Qualified) Responsible for setting achievable ... - Mar 07
... Ensured all deployments follow established processes to ensure quality, repeatability, efficiency and GMP/SOX compliance so customers are minimally impacted by changes in production. (Validated and Qualified) Responsible for setting achievable ... - Mar 07
Medical Device Assembler
San Jose, CA
... • Knowledge of GMP and GDP practices. • Able to work individually or as a team. • Performed final packaging of products. MEDICAL DEVICE ASSEMBLER Medtronic Sunnyvale, CA January 13, 2020 to May 11, 2020 • Connected and soldered t-tip parts for ... - Feb 26
... • Knowledge of GMP and GDP practices. • Able to work individually or as a team. • Performed final packaging of products. MEDICAL DEVICE ASSEMBLER Medtronic Sunnyvale, CA January 13, 2020 to May 11, 2020 • Connected and soldered t-tip parts for ... - Feb 26
Supply Chain Management
San Jose, CA, 95127
... Built and loaded projected Growth plans and New Product Introduction cut-in forecasts for $1 billion+ business plans, including FDA and GMP Procedures, and Spares/Field Service coverage. Management of 8+ key customer accounts and over $300 million ... - Feb 22
... Built and loaded projected Growth plans and New Product Introduction cut-in forecasts for $1 billion+ business plans, including FDA and GMP Procedures, and Spares/Field Service coverage. Management of 8+ key customer accounts and over $300 million ... - Feb 22
Lab Manager Senior
Fremont, CA
... Prepared the lab to pass the ISO inspection and become GMP certified. Concluded many overdue projects and increased revenues. vendor management, team development and management Project Lead/Scientist/Virologist, 5/2021-10/2022 Siemens Healthcare ... - Feb 19
... Prepared the lab to pass the ISO inspection and become GMP certified. Concluded many overdue projects and increased revenues. vendor management, team development and management Project Lead/Scientist/Virologist, 5/2021-10/2022 Siemens Healthcare ... - Feb 19
Medical Device Quality Control
Hillside, CA, 95030
... orderly and thorough data collection ●Trained to follow Good Manufacturing Practices (GMP), ISO 13485:2016, ISO 9001:2008, FDA 21 CFR 820 ●Detail-oriented, self-motivated team player, and capable of training other associates ●Ability to quickly ... - Feb 19
... orderly and thorough data collection ●Trained to follow Good Manufacturing Practices (GMP), ISO 13485:2016, ISO 9001:2008, FDA 21 CFR 820 ●Detail-oriented, self-motivated team player, and capable of training other associates ●Ability to quickly ... - Feb 19
Inventory Management Erp Systems
Morgan Hill, CA, 95037
... investigation, complete corrective action plan and all other processes required by ISO and internal guidelines plus adhering to cGMP & GMP (Good Manufacturing Practice rules Prospective Vendors: Sourced new product and service information, pricing, ... - Feb 19
... investigation, complete corrective action plan and all other processes required by ISO and internal guidelines plus adhering to cGMP & GMP (Good Manufacturing Practice rules Prospective Vendors: Sourced new product and service information, pricing, ... - Feb 19
Quality Assurance Regulatory Affairs
San Jose, CA
... Working experience and knowledge in GMP, ISO 9001, ISO 13485, and QSR. SKILLS Software Skills: Enzyme.com, Blue Mountain Regulatory Asset Manager, Smartsheet, MasterControl, NetSuite, DocuSign, 21 CFR Part 11 Compliance Adobe sign Quality Skills: ... - Feb 17
... Working experience and knowledge in GMP, ISO 9001, ISO 13485, and QSR. SKILLS Software Skills: Enzyme.com, Blue Mountain Regulatory Asset Manager, Smartsheet, MasterControl, NetSuite, DocuSign, 21 CFR Part 11 Compliance Adobe sign Quality Skills: ... - Feb 17
Fixed Asset Purchase Order
Union City, CA, 94587
... Achieve 85% score on GMP, 90% score on GAR Review and maintain files for Capital Projects (manage 5+ projects – budget analysis, tracking and reconciling), Material Safety and Data Sheet (MSDS) – Update files for about 200 + chemicals and raw ... - Feb 13
... Achieve 85% score on GMP, 90% score on GAR Review and maintain files for Capital Projects (manage 5+ projects – budget analysis, tracking and reconciling), Material Safety and Data Sheet (MSDS) – Update files for about 200 + chemicals and raw ... - Feb 13