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FDA resumes in Manchester, CT

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Resume alert Resumes 51 - 60 of 71

Customer Service Management

Farmington, CT
... Performs ad hoc reports and analysis to support statutory filings, (Port Authority Privilege Permits, USDA, FDA, Home Land Security and local regulatory agencies. Managing all financial, accounting and regulatory policy (FDA, USDA, Port Authority, ... - 2014 Jan 27

R&D/Lab Technician, Microbiology Lab Assistant, B.S. Biology

East Longmeadow, MA
... Inc., San Diego, CA, R&D/Lab Technician 7/2013- Present Hired as independent contractor to analyze and perform specific experiments with an aerosol inhalation device, through patient simulated use, in order to collect data for FDA analysis. ... - 2013 Oct 22

Medical Device Quality Assurance

West Springfield, MA
... , PMA processes • Knowledge of technical documents like eCTDs and STEDs • Knowledge of regulations and standards including FDA/USDA, Health Canada, cGMP, SOPs, cGCP, ICH guidelines and ISO standards • Sharpened understanding of the laws that govern ... - 2013 Aug 14

Creative Service Manager, Graphic Design

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

Quality Assurance Sales

New Britain, CT
... Proficient in GMP-research environment through following strictly FDA regulations and requirements. Excellent in maintenance, calibrations, alignments of sophisticated research equipment. Skilled in team mentoring and managing others. EXPERIENCE ... - 2013 Jun 04

Manager Sales

East Granby, CT
... Managing Partner: started and handled all aspects of business, from FDA certification, to import, marketing, sales, distribution, product support, accounting, product development. 5/2002 - PROMOTION spa, Altavilla VI, Italy 6/2006 Luxury goods ... - 2013 May 28

Medical Device Quality

Farmington, CT, 06032
... Support compliance to the FDA QSR 820, ISO 13485:2003 & 9001:2008, and ISO 14001, CE-mark 93/42/EEC, Canadian medical device Regulation part I, Japan PAL regulation and other mandatory domestic and international certification requirements. Attend ... - 2013 May 10

Manager Sales

Mansfield Center, CT
... - Responsible for documentations on company policies, safety programs, and training in meeting the requirements of Occupational Health and Safety Administration (OSHA) and FDA - Reduced Insurance Premiums through Risk Management Programs. - Reviewed ... - 2013 Apr 24

Electrical Engineer Manufacturing

Springfield, MA
... various control system initiatives, many based on Lean Manufacturing principles, that resulted in safety improvements and cost savings.Analyzed previously installed complicated control systems for understanding, documentation and FDA validation. ... - 2013 Feb 13

Health Project

West Hartford, CT, 06107
... These works support the company's clinical claims and application to FDA approval for marketing the products; Obtained solid data to extend its pending patents. 4) Submit 4 NIH SBIR grant proposals in FY06 - 2 were scored and I will resubmit. Two ... - 2012 Dec 02
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