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Resumes 61 - 70 of 116 |
Fairfield, CT
... Ensure the requirements of FDA standards and CGMP requirements are met. Schedule and participate in Lean Manufacturing events. Completed 80 hour certified course in Lean Manufacturing training and 16 hours of Dealing with resistance in implementing ...
- 2017 May 30
Shelton, CT, 06484
... classification, and regression Biomedical Product Development and Commercialization Fall 2015 Acquired an understanding of FDA and US Patent applications and procedures In depth look at market drivers and hurdles such as regulatory restraints, ...
- 2017 Apr 17
Ridgefield, CT, 06877
... of Arts in General Psychology GPA: 3.29 Experience Boehringer Ingelheim – Regulatory Reporter September 2015-Present Manage workflow by responsibly tracking expedited reports for safety reporting and prioritize based on company and FDA guidelines. ...
- 2017 Apr 04
Bridgeport, CT
... BIOMEDICAL AND COMPUTER SKILLS • Regulatory/Quality: FDA, ISO, GMP, Quality, Validation, Safety. • Technical computing software’s: COMSOL, MATLAB, SIMULINK. • Management proficiency: Customer support, Documentation, Wealth management, Business ...
- 2017 Feb 13
Darien, CT, 06820
... Oversee movement of inventory into the US complying with FDA paperwork in conjunction with the UK Supply team. Prepare and submit US Department of Commerce Census reports. Manage order processing, A/R and A/P functions and administrative staff. ...
- 2017 Jan 17
West Haven, CT, 06516
... Working knowledge of cost benefit analysis, direct labor optimization, profit & loss statements and yield variances Demonstrated ability to direct, coach, and train associates as well as plan, monitor and schedule work Working knowledge of FDA ...
- 2016 Nov 15
Waterbury, CT
... User Requirement Specifications for Fluidized Bed Dryer Installation and operational qualifications for the Mixer Analyzed and Discussed Quality Trends observed in FDA Warning Letters. Publications: Evaluation of the Hepatoprotective activity of ...
- 2016 Sep 19
Danbury, CT
... • Also knowledge of FDA, packaging, clean room and aseptic techniques. • JD Edwards trained and qualified, Process operator certified. Barr Pharmaceuticals Inc. NY 02/01 – 08/03 Manufacturing Technician • Was responsible audit of Batch Manufacturing ...
- 2016 Jul 20
Danbury, CT
... Conduct GLP studies with knowledge of R&D, QA and FDA regulatory requirements all according to BI SOPs as reference. Attend protocol meeting(s), coordinate with animal resource staff and execute experimental setup according to model system and drug ...
- 2016 Mar 16
Southbury, CT
... • Applications Development Expert • Automation Regression Expert • FDA CFR 21 Part-11 • Unit Testing • SDLC, Change Management • Quality Assurance and Best Practices • Functional Testing • Requirement Analysis • Development & Gap Estimates EDUCATION ...
- 2015 Nov 30