| Resume alert | Resumes 81 - 90 of 461 |
Logistic Coordinator
Brighton, MA
... * Brighton, MA 02135 617-***-**** adh2sh@r.postjobfree.com WORK HISTORY NanoEnTek America, Inc., Waltham, MA June 2020 – Oct 2020 Logistics Coordinator Coordinated international and domestic shipments of FDA approved medical products Processed ... - 2020 Nov 23
... * Brighton, MA 02135 617-***-**** adh2sh@r.postjobfree.com WORK HISTORY NanoEnTek America, Inc., Waltham, MA June 2020 – Oct 2020 Logistics Coordinator Coordinated international and domestic shipments of FDA approved medical products Processed ... - 2020 Nov 23
Data Engineer
Ipswich, MA
... Supported FDA Licensed/regulated medical/clinical Devices for sister company Datex-Ohmeda Implemented and maintained Enterprise Application Integration (EAI) interface solutions for major hospital installations in U.S. and Canada using the - 2020 Nov 19
... Supported FDA Licensed/regulated medical/clinical Devices for sister company Datex-Ohmeda Implemented and maintained Enterprise Application Integration (EAI) interface solutions for major hospital installations in U.S. and Canada using the - 2020 Nov 19
Nurse Practitioner Registered
Cambridge, MA
... overall Project Management of multi-center Neurological Disorders Clinical Research Trials • Member of multiple study trial teams, working with PI’s to develop protocols, amendments, consent forms and revisions in line with IRB and FDA regulations. ... - 2020 Nov 17
... overall Project Management of multi-center Neurological Disorders Clinical Research Trials • Member of multiple study trial teams, working with PI’s to develop protocols, amendments, consent forms and revisions in line with IRB and FDA regulations. ... - 2020 Nov 17
Safety Medical
Brookline, MA
... CSR, Synoptic CSR, and Supplemental CSR), IB updates, FDA briefing Documents, PRAC Response to Questions (RTQs), Risk Management Plan (RMPs), Risk Evaluation and Mitigation Strategy (REMS), Clinical Overview documents, PSURs, DSURs and PBRER. ... - 2020 Nov 16
... CSR, Synoptic CSR, and Supplemental CSR), IB updates, FDA briefing Documents, PRAC Response to Questions (RTQs), Risk Management Plan (RMPs), Risk Evaluation and Mitigation Strategy (REMS), Clinical Overview documents, PSURs, DSURs and PBRER. ... - 2020 Nov 16
Water Treatment Forklift Operator
Lowell, MA
... Maintain inventory locations within an FDA compliant warehouse. Pick internal build orders for manufacturing. Pick, pack and ship external customer parts orders utilizing FedEx and DHL. Participate in cycle counting activities. Shipper & Receiver ... - 2020 Oct 27
... Maintain inventory locations within an FDA compliant warehouse. Pick internal build orders for manufacturing. Pick, pack and ship external customer parts orders utilizing FedEx and DHL. Participate in cycle counting activities. Shipper & Receiver ... - 2020 Oct 27
Digital Marketing Manager
Waltham, MA
... Decisions Followed the industry regulations, GXPs, and FDA controls into Supply Chain optimizations using Sage Therapeutics guidelines Worked with vendors RFQ, RFP, SOWs and MSAs for performing the deployment of the Marketing Cloud (SFMC) (VEEVA). ... - 2020 Oct 21
... Decisions Followed the industry regulations, GXPs, and FDA controls into Supply Chain optimizations using Sage Therapeutics guidelines Worked with vendors RFQ, RFP, SOWs and MSAs for performing the deployment of the Marketing Cloud (SFMC) (VEEVA). ... - 2020 Oct 21
Regulatory Affairs
Boston, MA
... Coursework: The FDA Regulations, Therapeutics Product Development, Human Experimentation, Legal Issues in International Pharmaceutical Regulations (EMA), Global Impact of (eCTD) Submissions, Australia, Canada, Asian and Latin American regulatory ... - 2020 Oct 13
... Coursework: The FDA Regulations, Therapeutics Product Development, Human Experimentation, Legal Issues in International Pharmaceutical Regulations (EMA), Global Impact of (eCTD) Submissions, Australia, Canada, Asian and Latin American regulatory ... - 2020 Oct 13
Clinical Research
Concord, MA
... Skills Familiarity with clinical research documentation, ICH-GCP, FDA regulations Ability to multi-task, manage strategic deadlines in a fast-paced environment and work independently with minimal supervision Knowledge of Google Suite, Microsoft Word ... - 2020 Oct 13
... Skills Familiarity with clinical research documentation, ICH-GCP, FDA regulations Ability to multi-task, manage strategic deadlines in a fast-paced environment and work independently with minimal supervision Knowledge of Google Suite, Microsoft Word ... - 2020 Oct 13
Assistant Food Safety
Cambridge, MA
... Researched and developed vital quality assurance documentation, including Food Defense Program and Hazard Communication Program, in compliance with FDA, OSHA, and US Army Bioterrorism regulations for food safety. Communicated with customers and ... - 2020 Oct 08
... Researched and developed vital quality assurance documentation, including Food Defense Program and Hazard Communication Program, in compliance with FDA, OSHA, and US Army Bioterrorism regulations for food safety. Communicated with customers and ... - 2020 Oct 08
TCR/CAR discovery
Billerica, MA
... of vaccine vials • Evaluated data and prepared reports for component specifications in compliance with cGMP, cGLP and FDA by using Microsoft Excel spreadsheet • Ensured batch uniformity and integrity by communicating and submitting analysis ... - 2020 Sep 30
... of vaccine vials • Evaluated data and prepared reports for component specifications in compliance with cGMP, cGLP and FDA by using Microsoft Excel spreadsheet • Ensured batch uniformity and integrity by communicating and submitting analysis ... - 2020 Sep 30