| Resume alert | Resumes 71 - 80 of 295 |
Engineer Mechanical
Lowell, MA
... • Strong understanding of GMP (Good Manufacturing Practice) including GDP (Good Documentation Practice). • Working knowledge of SAP PLM, AutoCAD, Solidworks, SAS, Photoshop and MS Office. • Expertise in Product design and development using AutoCAD ... - 2020 Jun 08
... • Strong understanding of GMP (Good Manufacturing Practice) including GDP (Good Documentation Practice). • Working knowledge of SAP PLM, AutoCAD, Solidworks, SAS, Photoshop and MS Office. • Expertise in Product design and development using AutoCAD ... - 2020 Jun 08
Associate Director
Acton, MA
... - Familiar with QDoCC, OPM, SAP, QT9, and TrackWise - Familiar with 21 CFR 210, 211, 820, EudraLex GMP Guidance, and ISO 13485 - Vendor management and schedule audit plan and act as co-auditor during vendor site audit. - Familiar with different ... - 2020 May 06
... - Familiar with QDoCC, OPM, SAP, QT9, and TrackWise - Familiar with 21 CFR 210, 211, 820, EudraLex GMP Guidance, and ISO 13485 - Vendor management and schedule audit plan and act as co-auditor during vendor site audit. - Familiar with different ... - 2020 May 06
Clinical Research
Boston, MA
... • Regulations 21 CFR 812 (IDE), 814(PMA) and 820 (QSR or GMP), ISO 9001, Medical Device Reporting (MDR). • Regulations for Humanitarian Use Device, Orphan drug for rare diseases, IVDs and Combination Products and ICH guidelines. • Expedited pathways ... - 2020 Apr 02
... • Regulations 21 CFR 812 (IDE), 814(PMA) and 820 (QSR or GMP), ISO 9001, Medical Device Reporting (MDR). • Regulations for Humanitarian Use Device, Orphan drug for rare diseases, IVDs and Combination Products and ICH guidelines. • Expedited pathways ... - 2020 Apr 02
PD Manager
Medfield, MA
... Key skill/experience: ISO13485 standards, GLP/GMP Guidelines 4 years of biotech industry experience, with 3 years leading high throughput R&D team. 8 Years of Academic research lab management experience Product/Project Management 20+ Publication of ... - 2020 Mar 27
... Key skill/experience: ISO13485 standards, GLP/GMP Guidelines 4 years of biotech industry experience, with 3 years leading high throughput R&D team. 8 Years of Academic research lab management experience Product/Project Management 20+ Publication of ... - 2020 Mar 27
Engineering Quality Assurance
Arlington, MA
... EXPERIENCE: MedSource Technologies, Norwell, MA 020**-****-**** - 2004 Quality Assurance Systems Administrator/Supervisor • Successfully streamlined inspection criteria to ensure compliance with GMP guidelines thus increasing efficiency and ... - 2020 Jan 21
... EXPERIENCE: MedSource Technologies, Norwell, MA 020**-****-**** - 2004 Quality Assurance Systems Administrator/Supervisor • Successfully streamlined inspection criteria to ensure compliance with GMP guidelines thus increasing efficiency and ... - 2020 Jan 21
Quality Control inspector II, assembler II have lean six sigma traini
Lowell, MA
... Diploma in Electronics ADMINISTRATIVE SKILLS & SEMINARS Bilingual ISO-9001, 9002 GMP (Good Manufacturing Practice) RSA Course (Rheometrics Solids Analyzer) Handling Customer Inquiries Improving Your Performance Analyzing Work Processes Solving ... - 2019 Dec 23
... Diploma in Electronics ADMINISTRATIVE SKILLS & SEMINARS Bilingual ISO-9001, 9002 GMP (Good Manufacturing Practice) RSA Course (Rheometrics Solids Analyzer) Handling Customer Inquiries Improving Your Performance Analyzing Work Processes Solving ... - 2019 Dec 23
Medical Device Manager
Medford, MA
... analytical validation, technology transfer, GMP, GCP, CLIA, FDA, ISO guidance, troubleshooting 3 + years projects management experience: control documents, ANDA, PMA and 510(k) projects, IRB file Education Rice University, Houston, TX Dec. ... - 2019 Oct 17
... analytical validation, technology transfer, GMP, GCP, CLIA, FDA, ISO guidance, troubleshooting 3 + years projects management experience: control documents, ANDA, PMA and 510(k) projects, IRB file Education Rice University, Houston, TX Dec. ... - 2019 Oct 17
PharmD Patient Counseling, AE Reporting, CMS, Inventory P&L, DUR
Boxford, MA
... Enrolled in online management and GMP courses to further enhance knowledge and keep abreast of new industry developments. Seeking to leverage extensive technical background and communication skills as a worthy company asset. Skills Knowledge of ICH, ... - 2019 Oct 04
... Enrolled in online management and GMP courses to further enhance knowledge and keep abreast of new industry developments. Seeking to leverage extensive technical background and communication skills as a worthy company asset. Skills Knowledge of ICH, ... - 2019 Oct 04
Quality Assurance Director level
Boston, MA
... Proven ability to design and implement Quality concepts and controls into the GMP manufacturing as well as the GCP and GLP environments. Extensive experience in developing, managing and directing cGMP and GLP Compliance and Quality programs. In ... - 2019 Jul 30
... Proven ability to design and implement Quality concepts and controls into the GMP manufacturing as well as the GCP and GLP environments. Extensive experience in developing, managing and directing cGMP and GLP Compliance and Quality programs. In ... - 2019 Jul 30
Manager Customer Service
Dracut, MA
... •Responsible for all receiving •Entering material into Great Plains •Assigning lot numbers to controlled materials following GMP procedures, SOP’s •Issuing requested material into clean room bypass rooms •To perform cycle counts as requested and to ... - 2019 Jun 07
... •Responsible for all receiving •Entering material into Great Plains •Assigning lot numbers to controlled materials following GMP procedures, SOP’s •Issuing requested material into clean room bypass rooms •To perform cycle counts as requested and to ... - 2019 Jun 07