| Resume alert | Resumes 61 - 70 of 275 |
Medical Device Social Media
Jamaica Plain, MA
... quality review of Trial Master File (TMF) • Performed quality control review of documents and work as per GxP standards (GCP, GMP, GLP, GDP) Freyr Solutions, Princeton NJ Apr 2019 - Sep 2019 Regulatory Affairs Intern • Performed with DLP, SLP, RLP, ... - 2020 Jun 24
... quality review of Trial Master File (TMF) • Performed quality control review of documents and work as per GxP standards (GCP, GMP, GLP, GDP) Freyr Solutions, Princeton NJ Apr 2019 - Sep 2019 Regulatory Affairs Intern • Performed with DLP, SLP, RLP, ... - 2020 Jun 24
Chemical Engineering Pharmacy Technician
Burlington, MA
... Job responsibilities: Performing detailed and accurate record keeping for process documentation Developing and maintaining strong interpersonal relationships Working hand on to manufacture quality products Working within the guidelines of GMP ... - 2020 Jun 18
... Job responsibilities: Performing detailed and accurate record keeping for process documentation Developing and maintaining strong interpersonal relationships Working hand on to manufacture quality products Working within the guidelines of GMP ... - 2020 Jun 18
Research Assistant
Belmont, MA
... *, addqlk@r.postjobfree.com Belmont, MA 832-***-**** 1 PARISA ANSARI Bioanalytical Chemist Scientist A highly creative and innovative degree-qualified bio/analytical chemist researcher with hands-on working on GMP area. Extensive experience with ... - 2020 Jun 10
... *, addqlk@r.postjobfree.com Belmont, MA 832-***-**** 1 PARISA ANSARI Bioanalytical Chemist Scientist A highly creative and innovative degree-qualified bio/analytical chemist researcher with hands-on working on GMP area. Extensive experience with ... - 2020 Jun 10
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