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FDA resumes in Indianapolis, IN

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Resume alert Resumes 91 - 100 of 245

Attorney

Plainfield, IN
... • Conduct legal research and interpret laws, rules, and regulations related to business structuring, intellectual property, product development, FDA testing, and product imports. • Interpret, negotiate, and draft agreements and supporting documents ... - 2017 Jul 14

Customer Service Manager

Indianapolis, IN
... Developed many of the international shipping policies and procedures for exporting/importing non-FDA approved clinical trial drug for the newly formed and quickly growing department. Assumed training and mentoring role for the on-boarding of 10-20 ... - 2017 Apr 03

Manager Medical

Indianapolis, IN
... Served as customer liaison between drug submission teams and processing unit to expedite digital FDA submissions for fast-tracking of approval process. Formatted documents for FDA submissions using digital scanner and filled patent requests for ... - 2017 Mar 29

Management Quality

Indianapolis, IN
... Highly proficient in driving and ensuring all activities comply with ISO Standards, FDA regulations, current Good Manufacturing Practices (GMP’s), customer specifications, and all other applicable requirements. •Quality Management System •FDA, ISO & ... - 2017 Mar 24

Medical and Technical Writer and Project Management

Indianapolis, IN
... Update CMC submission modules based on FDA, EMA, or Ministry of Health feedback. Support new submissions by creating lists of the modules that need updating, assisting with the project management tasks, and collaborating with Subject Matter Experts ... - 2017 Mar 15

Maintenance Technician/ Electrician

Indianapolis, IN
... Worked in an FDA regulated environment." Work Quality and Quantity "8/10 - Very strong electrical skills. Was the go to guy for wiring/VFD/switch issues.” "Varied day by day. 2-3 hours of set up. Would stay until the job was done at the end of shift ... - 2017 Mar 15

Customer Service Manager

Indianapolis, IN
... inspection, Incoming Inspection, Final Inspection, ISO Standards, Nadcap Standards, AS9100, TS16949, Special Treatments, AMS 13165, AMS 2430, AMS 2432, J442, J443, J444, Many Military Specs and Manual, FDA Specs, and All of GEs repair manuals. ... - 2017 Mar 07

JD Edwards Finance/Distribution consultant as well as Project Manager

Greenwood, IN
... by Country: Tier One Automotive Supplier (7) Life Science Companies (2) Medical Device Manufacturer (2) (including FDA validation) Chemical Companies (2) International Bicycle Manufacturer (1) Tool & Die Manufacturer (1) Mining Company (2) ... - 2017 Feb 19

Sales Representative Chemical Engineering

Carmel, IN
... and JMP Working knowledge of Python Pharmaceutical Training: Know the procedure of pharmaceutical Industry Working knowledge of FDA regulations Understanding of SDTM and ADAM Other skills: Fluency in both Chinese and English CERTIFICATION 2011 SAS ... - 2017 Feb 04

Customer Service, Manufacturing, Supervisor

Fishers, IN
... *FDA Medical Device Manufacturing environment. *Scheduling shift production.*Good Manufacturing Practices(GMP). *Good Documentation Practices(GDP).*Standard Operating Procedures(SOP). *AS-400.*Forklift certified. *Monitoring employee attendance (ADP ... - 2016 Dec 15
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