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Resume alert |
Resumes 1 - 10 of 306 |
Waltham, MA, 02451
... -Extensive knowledge of government procurement, DOD, FAR, GMP regulations. Previously granted Top Secret clearance. -Excellent interpersonal skills to foster and fortify partnerships with subordinates, colleagues and upper level management. --Worked ...
- Sep 21
Devens, MA, 01434
... or abnormalities of products are happened, complying with all policies, work instructions, quality regulations, SOP’s, GMP’s, and GDP’s, supporting business needs by working overtime on the needs of basis assigned by managements, packaging and ...
- Sep 19
Boston, MA, 02111
... problem solving in collaboration with Quality Control, Manufacturing and Microbiology Departments Leader, Sartoflow Advanced antigen/antibody recycling project in the aseptic environment, instrument validation in the GMP and GLP environment. ...
- Sep 19
Boston, MA
... Assurance Intern Jan 2024 – Mar 2024 MEYER Vitabiotics ●Monitored the manufacturing processes of tablets, ensuring adherence to Standard Operating Procedures (SOPs) and Good Manufacturing Practices (GMP) as part of regulatory compliance initiatives. ...
- Sep 18
Charlestown, MA
... GCP, GMP, GXP, Regulatory affairs, Medical devices Management Skills Presentation Skills Proteomics analysis: Protein expression and purification; AKTA FPLC; ELISA; MSD; Luminex; ELISPOT, Western blot Serology Analysis; histology analysis Attention ...
- Aug 27
Dracut, MA
... Trained in GMP, QVR, ISO, EHS, EMS, GDP, OSHA, FDA and general regulatory compliance. US Army, Fort Devens MA 5/15-1/17 (Contractor) Office & Facilities Specialist – Base Wide Assistant to the DPW Facility Director overseeing 200 structures, 60 ...
- Jul 29
Cambridge, MA
... VT RF Deployment Lead (project) 2011- 11/2012 Build, deployed and QC Gatekeepers in a SGS infrastructure (collectors and repeaters) Implemented Signal collectors/routers (Cell+Wireless LAN, WAN + DSL) throughout the state of VT for GMP and CVPS. ...
- Jul 25
Andover, MA
... Provide support for GMP clinical manufacturing activities, including training, troubleshooting, data monitoring, process improvements, and documentation management. Develop reference standard material qualification strategy. Lead analytical activity ...
- Jul 15
Wilmington, MA, 01887
... Neurodyne Medical, Cambridge, MA 1996-2000 Lead Technician/ Production Manager Coordinator of all production activities and scheduling for FDA, GMP compliant biofeedback medical device company. Worked with design engineers building prototype ...
- Jul 10
Boston, MA
... Actively supports management and resolution of key issues which impact product release at CMOs Review deviations, supplier change notification, (SCN), SOP procedures, CAPA, and reports to ensure compliance to internal and GMP standards. Support ...
- Jul 08