|
Resume alert |
Resumes 71 - 80 of 94 |
Hamden, CT
... year • Created and commercialized Fixt™ Introducer • Authored component / product qualifications in preparation of FDA submission • Design Council Facilitator • Supervised / Mentor design team personnel and other staff in support of project goals. ...
- 2014 Aug 09
Oakville, CT
... Newark NJ 07106 Telephone: 973-***-****) cell: 973-***-**** SUMMARY: Goal oriented and result driven professional with knowledge of Pharmacovigilance, ICH-GCP,GLP and FDA/EU regulations in Pharmaceuticals and Biotechnology operational settings. ...
- 2014 Aug 09
Fairfield, CT
... reporting of Litigation cases to FDA in timely manner and in accordance with FDA regulations u Accountable for all product complaints from inception to closure as well as corrective action follow-up; submission of 510(K) and PMA applications u ...
- 2014 Jul 31
Milford, CT
... including FDA quality systems, standard operating procedures, auditing, monitoring, investigations, training, documentation practices, corrective and preventive actions, and interpretation of laws and regulations governing quality and compliance. ...
- 2014 Jul 31
Rocky Point, NY
... Was responsible to inform FDA for every procedure made Clinical Research Coordinator, Intec Pharma Ltd., Jerusalem, Israel, October 2010 - May 2011 Start-up Drug development Company . Managed protocol between patients with Parkinson's disease, ...
- 2014 Jun 20
Hamden, CT
... Prepare audit materials and participate in various audits ranging from NY/NJ Port Authority, Homeland Security, USDA, FDA, SBA, various banking institutions, IRS, States of CT and NY, etc. 35. Strategic planning and system conversion to move to more ...
- 2014 Mar 13
Naugatuck, CT
... Software Testing & Validation Test Planning & Reporting SOP Administration Test & Use Case Development SDLC Methodologies FDA GxP Regulations User & Functional Requirements Data Warehousing Vendor & Cient Relations Business Intelligence User ...
- 2014 Jan 21
Meriden, CT, 06450
... Utilize innovative organizational skills to enhance creative team productivity while complying with corporate • Promotional campaigns policies along with FDA and ISO regulations. • Mailers/mailings • Medical device • Strong work ethic and enthusiasm ...
- 2013 Aug 07
Hamden, CT, 06514
... Ensure proper cleaning and sanitation of the plant through preventive maintenance programs that meet USDA, OSHA and FDA regulations. Manage a 23-person administrative and operations staff in all personnel matters. Key Achievements: - Improved bottom ...
- 2013 Jul 18
Stratford, CT, 06614
... location in USA following their quality controls Organization Project Details Role Duration Covidien Inc., Mansfield, MA USA DHF Remediation of Dialysis Catheters The DHF of hemodialysis catheters were remediated as per FDA / TUV guidelines. ...
- 2013 Jun 05