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Associate Director, Regulatory Affairs
Skingenix - Ontario, CA
applications and requiredamendments, FDA CMC related correspondences, and ... knowledge and working experience with FDA IND lifecycle management required.
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Associate Scientist I - QC Analytics Job - new
Yoh - Vacaville, CA
Yoh has a contract opportunity for an Associate Scientist I: QC Analytics to join our ... Job Qualifications: - Knowledge of cGMP and FDA guidelines, applicable State and Foreign...
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Associate Director Clinical Research
Questcor - Columbia, MD +1 location
FDA related research and supports all non-FDA company sponsored research. ... Safety/Pharmacovigilance, Medical Affairs, Pharmaceutical Development, Sales/Marketing)...
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PQA Associate Analyst
Abbott Laboratories - Alameda, CA
Skills/Experience Requirements Basic Qualifications: Working knowledge of FDA Code of Federal Regulations as it applies to medical device manufacturing, including cGMP, ISO...
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CRA IV Study Manager
Abbott Laboratories - Alameda, CA
clinical research. Extensive knowledge of FDA regulatory requirements. CORE JOB RESPONSIBILITIES: Responsible for compliance with quality system regulations. Knowledge of...
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Logistics Associate - new
BioMarin Pharmaceutical - Novato, CA
Requisition Number 12-0089 Post Date 4/6/2012 Title Logistics Associate City Novato Descri ... and other international shipping required Pharmaceutical/biotech distribution...
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Associate Director, Client Account Manager, Finance
Pharmaceutical - Boston, MA
SOX regulated applications Knowledge of FDA Regulated Systems Environments including ... a plus Previous experience working in a pharmaceutical environment highly preferred...
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Sr Associate, Regulatory Affairs City - new
BioMarin Pharmaceutical - Novato, CA
Job Details Requisition Number 11-0200 Post Date 12/14/2011 Title Sr Associate, Regulatory ... Knowledgeable at interpreting and analyzing FDA and industry-related regulations and...
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Associate Project Engineer, QA Validation - new
BioMarin Pharmaceutical - Novato, CA
a plus). Understanding and familiarity with FDA & European regulatory requirements, guidelines, and recommendations for process validation expectations. Proficiency with technical...
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Senior CRA - Clinical Operations - Liver Disease - new
Gilead - Foster City, CA
meet all requirements for Clinical Research Associate position and have demonstrated ... Working knowledge of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the c...
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