| Resume alert | Resumes 41 - 50 of 183 |
Plc Engineer
Pleasanton, CA
... Practicing all Safety manufacturing standards regulated by OSHA, NFPA 70E and FDA Regulations. PLC and SCADA system assistant: California State University: Dept of Industrial Technology: Dr Athanasios Alexandrou: Jan 2018 to May 2019 Design PLC ... - 2020 May 26
... Practicing all Safety manufacturing standards regulated by OSHA, NFPA 70E and FDA Regulations. PLC and SCADA system assistant: California State University: Dept of Industrial Technology: Dr Athanasios Alexandrou: Jan 2018 to May 2019 Design PLC ... - 2020 May 26
Supply Chain
Dublin, CA
... ●Systems alignment validation, recommendations, and FDA and SOX compliancy evaluation with system setups, testing, validation documentation requirements and helped the client with the development of documentation, test script development, validation ... - 2020 May 18
... ●Systems alignment validation, recommendations, and FDA and SOX compliancy evaluation with system setups, testing, validation documentation requirements and helped the client with the development of documentation, test script development, validation ... - 2020 May 18
Medical Engineer
Castro Valley, CA
... Trained and certified in GMP/FDA, Clean room Suites and Analytical Laboratories. Duties include performing formulations and assisting in production goals, sterilizing instruments, storing along with accurate documentation of work performed. Bio ... - 2020 Jan 28
... Trained and certified in GMP/FDA, Clean room Suites and Analytical Laboratories. Duties include performing formulations and assisting in production goals, sterilizing instruments, storing along with accurate documentation of work performed. Bio ... - 2020 Jan 28
Sap Service
San Ramon, CA
... with Philips for Application Maintenance and Support and “unique device identifier” (UDI) Implementation, this project is related to FDA compliance intended primarily to provide information about submitting data to the database for device Labelers. ... - 2019 Nov 05
... with Philips for Application Maintenance and Support and “unique device identifier” (UDI) Implementation, this project is related to FDA compliance intended primarily to provide information about submitting data to the database for device Labelers. ... - 2019 Nov 05
Medical Device Quality Engineer
Castro Valley, CA
Elson Young Mobile Phone: 510-***-**** ● Email: adajxv@r.postjobfree.com Objective Highly experienced Quality Assurance professional seeking a position in an organization where I can utilize my skills, experience, and knowledge towards FDA and ... - 2019 Oct 09
Elson Young Mobile Phone: 510-***-**** ● Email: adajxv@r.postjobfree.com Objective Highly experienced Quality Assurance professional seeking a position in an organization where I can utilize my skills, experience, and knowledge towards FDA and ... - 2019 Oct 09
Manager Engineer
Vallejo, CA
... Hyper-V Virtual-servers for monitoring dashboards - wall-monitors, Solarwinds, Event Log Analyzer Coordinated IT Operations to design, manage and deploy server environments Maintained GxP documentation vault for FDA audits Select Staffing S.B. ... - 2019 Oct 01
... Hyper-V Virtual-servers for monitoring dashboards - wall-monitors, Solarwinds, Event Log Analyzer Coordinated IT Operations to design, manage and deploy server environments Maintained GxP documentation vault for FDA audits Select Staffing S.B. ... - 2019 Oct 01
Quality Compliance Engineer
Dublin, CA
... Reddy’s - Shreveport, Louisiana – 2013-2017 Operations Manager for Oral Solid Dose Managed twelve employees responsible for the Coating, Printing & Packaging Operations Ensured adherence to all FDA guidelines and regulatory compliance Project leader ... - 2019 Aug 21
... Reddy’s - Shreveport, Louisiana – 2013-2017 Operations Manager for Oral Solid Dose Managed twelve employees responsible for the Coating, Printing & Packaging Operations Ensured adherence to all FDA guidelines and regulatory compliance Project leader ... - 2019 Aug 21
Manager Management
San Ramon, CA
... Excellent knowledge in FDA and EMA regulations and cGMP, ICH guidelines (Q8, Q9, Q12) Knowledge of writing standard operating procedures (SOPs), data capture and quality review, analytical methods, assay validation, and documents for regulatory ... - 2019 Jun 10
... Excellent knowledge in FDA and EMA regulations and cGMP, ICH guidelines (Q8, Q9, Q12) Knowledge of writing standard operating procedures (SOPs), data capture and quality review, analytical methods, assay validation, and documents for regulatory ... - 2019 Jun 10
Manufacturing Supply Chain
Pleasanton, CA
... Familiar with ISO standards, 5S system and FDA regulations. Proficient with GLPs cGMP and pharmaceutical industry procedures. Work Experience: Renewable Energy Group SSF, CA. 94080 Title: Senior Process Tech. II 12/15 – Present Solazyme Inc. SSF, CA ... - 2019 Apr 27
... Familiar with ISO standards, 5S system and FDA regulations. Proficient with GLPs cGMP and pharmaceutical industry procedures. Work Experience: Renewable Energy Group SSF, CA. 94080 Title: Senior Process Tech. II 12/15 – Present Solazyme Inc. SSF, CA ... - 2019 Apr 27
Quality Assurance Specialist
Antioch, CA
Katya Kramer Antioch, CA ***** 510-***-**** ac8myw@r.postjobfree.com Summary: Goal oriented and self-motivated with 14 years of experience in medical device industry, of which 8 years include production supervisory in an FDA and ISO-regulated ... - 2019 Feb 28
Katya Kramer Antioch, CA ***** 510-***-**** ac8myw@r.postjobfree.com Summary: Goal oriented and self-motivated with 14 years of experience in medical device industry, of which 8 years include production supervisory in an FDA and ISO-regulated ... - 2019 Feb 28