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biological, chemical and physical analyses on pharmaceutical products (biologics and drugs) through all stages of the manufacturing process from incoming raw material through finished goods including at a minimum; in-process testing, final...
EmployerQualifications(MINIMUM) Undergraduate degree or its international equivalent in clinical, science, or healthrelated field from an accredited institution; a licensed healthcare professional (i.e., registered nurse); or equivalent...
and other international markets. Experience in domestic and international regulatory approval of labeling artwork, ... Ability to research laws/regulations in various international markets and work with local outside counsel, regulatory co...
e synthesis and HPLC purification, as well as a strong background in organic chemistry. ?Post-Graduate or Graduate, with strong peptide synthesis experience in research will be considered. ?Some Pharmaceutical or biotech experience...
product line to most of the world's top companies in the pharmaceutical, biotech, industrial, educational, ... are registered trademarks of VWR International, LLC. VWR International, LLC is aware of fraudulent e-mails...
experiments in the R&D lab employing the disciplines of pharmaceutical and food sciences and by maintaining the laboratory workspace, equipment and inventory. DETAILED RESPONSIBILITIES/DUTIES: Document all experiments and results in a...
operations and government regulations pertaining to pharmaceutical and medical device manufacturing labs. 2. Must have the ability of managing complex projects and resolving complex lab. issues. 3. Must possess excellent supervisory and...
VWR International, LLC, headquartered in Radnor, Pennsylvania, is a global laboratory supply and distribution company ... are registered trademarks of VWR International, LLC. VWR International, LLC is aware of fraudulent e-mails...
POSITION SUMMARY STATEMENT: The AE Representative will work in a cross-functional capacity to support Herbalife's Adverse Event Reporting System. The AE Representative will be responsible for collecting, organizing and submitting adverse...
a validation function in a cGMP regulated industry such as pharmaceutical, medical device, plasma fractionation or biotechnology. Physical Demands & Working Envuironment: Must be able to lift, push, pull and carry up to 50 lbs. Must be...
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