|
Resume alert |
Resumes 41 - 50 of 82 |
West Warwick, RI, 02893
... Dartmouth Major: Bachelor of Science, Bioengineering, May 2017 Related Course Work Biomeasurment and control (instrumentation), FDA regulation & Classification, Medical ultrasound, Biomedical Devices, Biostatistics, Biomaterials, Biomechanics, ...
- 2017 Sep 21
Foxborough, MA
... Developed functional specifications, software test specifications (for FDA validation), Verification and Validation of the software including IQs, OQs, PQs, system configuration and Batch Unit Operations (i.e. Fermentation, reactor, centrifuge, ...
- 2017 Sep 14
North Attleborough, MA
... • Facilitated numerous performance and talent management workshops with all levels of the organization • Represented HR in all internal, inter-company, and external audits (FDA and ISO) • Facilitated corporate culture surveys; implemented programs ...
- 2017 Apr 24
Bristol, RI, 02809
... oThe project also took into consideration the business aspect, FDA approval, intellectual property, and quality control. APPLICATIONS: Bioengineering Laboratory Work: oLab work included; the creation of a respiration measurement device using a ...
- 2017 Apr 01
Killingly, CT
... PROFESSIONAL EXPERIENCE Tower Laboratories, Ltd January 2008 to April 2016 Centerbrook, Ct Position: Compliance Manager Duties and Responsibilities: Ensure corporate compliance to FDA cGMP regulations in Drug, Medical Device and Dietary Supplement ...
- 2016 Jul 10
Providence, RI
... Good leadership skills, technical skills, and FDA/Regulatory knowledge. MS Excel, Word, Power Point, and Outlook Bilingual (English-Spanish WORK EXPERIENCE American Wear Uniforms-East Orange, NJ 2015-Present Assistant Manager/Production Administered ...
- 2015 Dec 20
Douglas, MA
... Have familiarity with Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) validation protocol for biotech, pharmaceutical and chemical industries for FDA’s Rule 21 CFR Part 11 compliance. TECHNICAL ...
- 2015 Dec 10
Franklin, MA
Sita Dahal acso87@r.postjobfree.com SUMMARY Experience in Process Validation/Equipment Validation, Risk Management, Design of Experiments, Process Improvement and Quality Control in compliance with FDA regulations. Extensive validating experience in ...
- 2015 Dec 05
Foxborough, MA, 02035
... • Laboratory Validation testing was written, organized and completed using the requirement documentation from the testing or equipment suppliers, on time and completed within company and FDA guidelines. • Daily Quality Control was processed on all ...
- 2015 Oct 05
Fall River, MA
... Participated in all ISO and FDA audits as it pertained to products within my responsibility. Senior company manager leading the development of medical devices. Single use sterile disposables. Managed multiple projects through “Phase Gate” ...
- 2015 Jun 04