ASP Supplier Manager - (Job Number: 0800293) |
| ASP Supplier Manager - (Job Number: 0800293) DescriptionAdvanced Sterilization Products ... |
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Manager, Clinical Data Management - (Job Number: 0715365) |
| Manager, Clinical Data Management - (Job Number: 0715365) DescriptionResponsibilities: T... |
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Director, Compliance - (Job Number: 0804056) |
| Director, Compliance - (Job Number: 0804056) DescriptionAdvanced Sterilization Products,... |
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LABORATORY |
| LAB CLS for lab in S. O.C. F/T &/or PT avail. Sal., Bnfts, 401k, sign up bonus. Fax:949-369-9220 or ... |
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Project Manager - Regulatory |
| REGULATORY AFFAIRS PROJECT MANAGERSummary:
Profitable Medical Device Company in Irvine is ... |
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PHARMACEUTICAL SALES OPPORTUNITIES WITH GLAXOSMITHKLINE (GSK) |
| PHARMACEUTICAL SALES OPPORTUNITIES WITH GlaxoSmithKline
(see mandatory pre-application process ... |
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VP, Customer Care |
| Syneron is a leading and rapidly growing medical laser company involved in the design, development, ... |
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Project Engineer / 64 |
| Position Description:Since its founding in 1839, B. Braun has built an unparalleled store of ... |
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ASSOCIATE SCIENTIFIC DIRECTOR (licensed) |
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Job Summary
Reports to licensed Medical or Scientific Director and is responsible ... |
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Project Specialist
| Details |
Country: USA
Location: California-Orange County Irvine, CA
Total applied: 14 Job Category:Project/Program Management
Location:Irvine, CA 00000
Occupations:Project Management
Career Level:Experienced (Non-Manager)
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Project Specialist
Join us at the forefront of scientific discovery! At Bio-Rad Laboratories, you will participate in exciting new developments at the cutting-edge of science and technology. Our teams of dedicated professionals work together in an entrepreneurial atmosphere, providing a broad range of innovative tools and services to the clinical diagnostics and life science research markets. Bio-Rad was founded more than 40 years ago, and we are recognized as a world leader in science and research. Visit us at www.bio-rad.com Manage new or modified product development activities in compliance with regulatory and company procedures and policies. Coordinate creation and maintenance or related project documentation (plans, schedules), monitor project activities to ensure schedule is being met and Design History File is complete. Facilitate resolution of team/project issues, support other Project Managers as needed. Expected travel approximately 25%. Education: BA/BS in Biology, Chemistry or other technical field or equivalent.Experience: Minimum 1 year experience managing projects with 3-5 years experience in a similar, FDA regulated industry.Skills: Knowledge of FDA and ISO 13485 regulations, particularly relating to Design Control, good organizational, interpersonal, verbal communication and writing skills, experience in managing multi-disciplinary teams, ability to multi-task, proficient in Microsoft Word, Excel, Power Point and Project.
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