| Resume alert | Resumes 91 - 100 of 746 |
Quality Engineer Document Control
Milpitas, CA, 95035
... SURGICAL – Santa Clara, CA Vice President of Quality Assurance Responsible for developing, implementing, and maintaining a quality management system compliant with FDA QS Regulation, EN/ISO 13485, MDD, and Canadian Medical Devices Regulations. ... - 2022 Nov 08
... SURGICAL – Santa Clara, CA Vice President of Quality Assurance Responsible for developing, implementing, and maintaining a quality management system compliant with FDA QS Regulation, EN/ISO 13485, MDD, and Canadian Medical Devices Regulations. ... - 2022 Nov 08
Pharmacovigilance Scientist
Fremont, CA
... clients’ procedures and international drug safety regulations including- ICH guidelines on safety and efficacy, Volume 9A, FDA guidelines, CIOMS, new EU PV legislation Drug Safety Associate, Johnson & Johnson Pharmaceuticals, New Brunswick, NJ Sep ... - 2022 Oct 19
... clients’ procedures and international drug safety regulations including- ICH guidelines on safety and efficacy, Volume 9A, FDA guidelines, CIOMS, new EU PV legislation Drug Safety Associate, Johnson & Johnson Pharmaceuticals, New Brunswick, NJ Sep ... - 2022 Oct 19
Business Analyst Qa Lead
San Jose, CA
... Medical Device software test experience Understanding and practical exposure to FDA regulations LEADERSHIP EXPERIENCE Ability to embrace change in adding Technology domain to Medical / Health care domain Led QA Team for Nuzpapr.com EDUCATION Quality ... - 2022 Oct 09
... Medical Device software test experience Understanding and practical exposure to FDA regulations LEADERSHIP EXPERIENCE Ability to embrace change in adding Technology domain to Medical / Health care domain Led QA Team for Nuzpapr.com EDUCATION Quality ... - 2022 Oct 09
Mechanical Assembler
San Jose, CA, 95121
... of productivity based on calculating Quantity of Product/Time(minutes) Promotion employees interview Verify employees protocol check up Verify FDA regulations, SOP, MIP, Blue Prints, BOM, Kit, Software, Labels, Employees’ signature, Date and Time. ... - 2022 Oct 04
... of productivity based on calculating Quantity of Product/Time(minutes) Promotion employees interview Verify employees protocol check up Verify FDA regulations, SOP, MIP, Blue Prints, BOM, Kit, Software, Labels, Employees’ signature, Date and Time. ... - 2022 Oct 04
Safety Officer Program Manager
San Ramon, CA
... that touches the baby’s eye to locate indicators to catch diseases early · Secured FDA and ISO approvals and sold devices worldwide · First to introduce product software validation concepts to Mattson, building the system and teaching the benefits. ... - 2022 Oct 04
... that touches the baby’s eye to locate indicators to catch diseases early · Secured FDA and ISO approvals and sold devices worldwide · First to introduce product software validation concepts to Mattson, building the system and teaching the benefits. ... - 2022 Oct 04
Process Server Service Delivery
Pleasanton, CA
... FDA-CFR 21 Part 11 Responsible for Product Roadmap, Architecture & Design, leading Development & Testing of ECProc-BPM an Engineering/Construction domain BPM solution for end-to-end Project/Tasks, Personnel, Materials, Equipment resource management. ... - 2022 Sep 25
... FDA-CFR 21 Part 11 Responsible for Product Roadmap, Architecture & Design, leading Development & Testing of ECProc-BPM an Engineering/Construction domain BPM solution for end-to-end Project/Tasks, Personnel, Materials, Equipment resource management. ... - 2022 Sep 25
QC final inspections
San Jose, CA
... Troubleshooter/QC Analyst in an FDA/ GMP and fast pace medical device manufacturing environment seeking new opportunity to learn and to contribute to success of the organization. SUMMARY : Failure investigation and root cause analysis, finish ... - 2022 Sep 08
... Troubleshooter/QC Analyst in an FDA/ GMP and fast pace medical device manufacturing environment seeking new opportunity to learn and to contribute to success of the organization. SUMMARY : Failure investigation and root cause analysis, finish ... - 2022 Sep 08
Oracle Developer Production Engineer
San Carlos, CA
... to pull Data from SAP using Shell Scripts, PL/SQL and SQL Loader • Development of Custom Applications using Developer 6i/9i • Database validation using DQ, IQ, OQ and PQ for FDA Validated Systems • Application Support for Clinical Applications eg. ... - 2022 Aug 05
... to pull Data from SAP using Shell Scripts, PL/SQL and SQL Loader • Development of Custom Applications using Developer 6i/9i • Database validation using DQ, IQ, OQ and PQ for FDA Validated Systems • Application Support for Clinical Applications eg. ... - 2022 Aug 05
Fork Lift Manufacturing Associate
Hayward, CA
... -Adhered to general safety rules, manufacturing procedures, company policies and procedures, QSR AND FDA regulations. SHIPPING AND RECEIVING CLERK- LEAD - Over 10 years hands on experience in shipping and receiving clerk capacity - Certified ... - 2022 Jul 07
... -Adhered to general safety rules, manufacturing procedures, company policies and procedures, QSR AND FDA regulations. SHIPPING AND RECEIVING CLERK- LEAD - Over 10 years hands on experience in shipping and receiving clerk capacity - Certified ... - 2022 Jul 07
Selenium Manual Testing
Pleasanton, CA
... Accenture Life Sciences Cloud (ALSC), India Sep 2016 – Apr 2020 Clients: Bayer, Merck, GSK, Lilly, Pfizer Responsible for ensuring the clinical trial data received from InForm or any other EDC systems is in the pre-approved FDA compliant format. The ... - 2022 Jun 19
... Accenture Life Sciences Cloud (ALSC), India Sep 2016 – Apr 2020 Clients: Bayer, Merck, GSK, Lilly, Pfizer Responsible for ensuring the clinical trial data received from InForm or any other EDC systems is in the pre-approved FDA compliant format. The ... - 2022 Jun 19