| Resume alert | Resumes 51 - 60 of 417 |
I am retired management from the health care industry.
Lake Zurich, IL
... FDA’s Quality System Regulations 21CFR820; ISO 13485; ISO 14971 Key strengths include: DHF improvements/remediation for legacy products. MDR – new classification system, conformity assessment paths, Annex I requirements, technical documentation, CE ... - 2023 Jan 18
... FDA’s Quality System Regulations 21CFR820; ISO 13485; ISO 14971 Key strengths include: DHF improvements/remediation for legacy products. MDR – new classification system, conformity assessment paths, Annex I requirements, technical documentation, CE ... - 2023 Jan 18
Plant Manager Production Supervisor
Elgin, IL
... Extensive experience dealing with USDA, FDA, GMP, HACCP and AIB Proven ability to build successful teams, manages with collaborative and participative style to bring out the best in team, build teams and organization that can function effectively ... - 2022 Dec 23
... Extensive experience dealing with USDA, FDA, GMP, HACCP and AIB Proven ability to build successful teams, manages with collaborative and participative style to bring out the best in team, build teams and organization that can function effectively ... - 2022 Dec 23
General Manager Arabic
Morton Grove, IL
... Operating Procedures for all manufacturing processes • Restructured the Drug Master File for the corporation compliance with the FDA • Implemented the usage of ERP software for manufacturing/accounting to improve the accuracy of business execution, ... - 2022 Oct 15
... Operating Procedures for all manufacturing processes • Restructured the Drug Master File for the corporation compliance with the FDA • Implemented the usage of ERP software for manufacturing/accounting to improve the accuracy of business execution, ... - 2022 Oct 15
Accounts Payable Corporate Controller
Park Ridge, IL
... month end close from 30 days to 5 day close Due Diligence for Licensing Deal Worked with Quality team on new product FDA approval AQUESTIVE THERAPUETICS INC (MAY 2018 to Nov 2018) (Consultant) Area CFO Responsible for Accounting, IT Projects, ... - 2022 Sep 19
... month end close from 30 days to 5 day close Due Diligence for Licensing Deal Worked with Quality team on new product FDA approval AQUESTIVE THERAPUETICS INC (MAY 2018 to Nov 2018) (Consultant) Area CFO Responsible for Accounting, IT Projects, ... - 2022 Sep 19
Data Entry Clinical Research
Schaumburg, IL
... Proficient working knowledge of the regulations (Food and Drug Administration (FDA), Good Clinical Practice (GCP), International Committee on Harmonization (ICH), ISO, etc). Organizational awareness to operate in cross-functional teams and provides ... - 2022 Jul 07
... Proficient working knowledge of the regulations (Food and Drug Administration (FDA), Good Clinical Practice (GCP), International Committee on Harmonization (ICH), ISO, etc). Organizational awareness to operate in cross-functional teams and provides ... - 2022 Jul 07
Quality Engineer Injection Molding
Glen Ellyn, IL
... material, assigned new part number and updated EC notice and drawing in accordance with EC, FDI, FDA and Iso 13485 for medical devices • Examined medical and electronic devices in compliance with ISO 14971 to reduce risks ADDITIONAL WORK EXPERIENCE - 2022 Jun 14
... material, assigned new part number and updated EC notice and drawing in accordance with EC, FDI, FDA and Iso 13485 for medical devices • Examined medical and electronic devices in compliance with ISO 14971 to reduce risks ADDITIONAL WORK EXPERIENCE - 2022 Jun 14
Mechanical Engineer Manufacturing
Villa Park, IL
... Manufacturing Engineer (06/2002 – 02/2003) Contract Position assisting the manufacturing team in implementing new processes, writing work instructions and quality plans, and developing process validations for FDA/GMP approval on a new production X ... - 2022 Jun 04
... Manufacturing Engineer (06/2002 – 02/2003) Contract Position assisting the manufacturing team in implementing new processes, writing work instructions and quality plans, and developing process validations for FDA/GMP approval on a new production X ... - 2022 Jun 04
Manufacturing Supervisor Injection Molding
Elgin, IL
... for four [4] aseptic SFS [Seal-Fill-Seal] Galaxy machines, to ensure that manufacturing goals and project deadlines are in compliance with current good manufacturing practices [cGMP’s] FDA guidelines and any other regulators that could apply. ... - 2022 Apr 30
... for four [4] aseptic SFS [Seal-Fill-Seal] Galaxy machines, to ensure that manufacturing goals and project deadlines are in compliance with current good manufacturing practices [cGMP’s] FDA guidelines and any other regulators that could apply. ... - 2022 Apr 30
Business Analyst Analytical Chemist
Naperville, IL
... chemistry techniques for chemical analysis ●Worked with legal teams to ensure data capture in LIMS for drug development was FDA compliant ●Created Current State and Future state business and functional flows ●Explained requirements to developer team ... - 2021 Jul 27
... chemistry techniques for chemical analysis ●Worked with legal teams to ensure data capture in LIMS for drug development was FDA compliant ●Created Current State and Future state business and functional flows ●Explained requirements to developer team ... - 2021 Jul 27
Test Analyst Lead
Schaumburg, IL
... Demonstrated expertise in FDA 21 CFR Part 11 electronic documentation and Part 820 CGMP quality system regulation standards. Engineered productivity through integrated software automation and control by applying programmable logic controllers (PLC), ... - 2021 Jun 23
... Demonstrated expertise in FDA 21 CFR Part 11 electronic documentation and Part 820 CGMP quality system regulation standards. Engineered productivity through integrated software automation and control by applying programmable logic controllers (PLC), ... - 2021 Jun 23