I seek an opportunity in which my experience, interests, training, education and insight compliment and contribute to the goals and mission of my employer. An environment that fosters my desires to learn and develop new skills is essential. I want to be inspired by my colleagues. Opportunities for career advancement and promotion are important factors that will influence my decision to accept an employment offer.
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Analytical Chemistry, Principal Investigator, Project Director, Project Management, Electroanalytical chemistry, Electrochemistry, Biosensors, Sensors, Diagnostics , Prognostics, in vitro diagnostics, Biomarkers, Materials, Supramolecular Chemistry, Polymers, Surface Characterization, Grant, Thin Films, Sol-gel, Immunoassay, Aptamer
Brenda is a Technical Writer and Quality Assurance Regulatory Document Specialist with over ten years of experience in the pharmaceutical industry.
She has extensive experience with all types of document project work, including writing, editing, formatting. She has experience as a team member for non-conformance investigations (NCs) and Corrective Action and Preventative Actions (CAPAs).
Her analytical and research skil...
I am interested in a Project Manager or related position requiring multitasking and organizational skills to oversee multiple projects. I have eight years experience in the biotech/pharmaceutical industry. With the scientific, laboratory and management skills I have accrued over the years, I can perform tasks without supervision. I am looking for a position that allows further personal and professional growth.
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Global Clinical Trials Project Management, ICH, GCP, GLP knowledge, Research Associate , Independent Research , Preclinical trial management, Oncology/Chemotherapeutic drug discovery and development
High potential research scientist looking for a balanced work culture that promotes excellence in individuals and team dynamics in order to achieve milestones in drug development and its clinical applications.
Gain entry into online Project mananagement Certifacte program and apply skills gained to achive higher level of accomplishment.
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Research & Development, GLP, Bioanalytical Assays, Immunoassay
Gary Plunkett
4392 Pine Harbor Drive
Denver, NC 28037
Glp66@live.com
310-418-1509
To Whom It May Concern:
I have been in the high technology aerospace industry my entire career with ultimate program/department responsibility in Program/Project Management, Contracts, Marketing, Sales, Operations, and Product Support/Customer Service as described in the enclosed resume.
I have extensive experience in both commercial and ...
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Business Management, Operations, Program Management, Sales, Marketing, Contracts
A degreed professional with over 4 years of experience in the pharmaceutical/Biotech industry with multi-functional Regulatory, Clinical and Quality background. Demonstrated ability to expand beyond the scope of assigned responsibilities to gain proficiency in new areas. Responsibilities have ranged from managing the preparation, submission of INDs, BLAs, ANDAs/NDA, to reviewing QMS, essential regulatory documents to ensure...
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Regulatory Affairs, Clinical Research, FDA, GCP, GCP, ICH, GLP, Pharmaceuticals, Quality Assurance
Application for chemical research scientist/process development chemist position
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synthetic organic chemist , medicinal chemistry, process development, scale-up of pharmaceutical chemicals, GLP/cGMP processes, HPLC, LC/MS, GC/MS, NMR, FT-IR, DSC, Karl Fisher, XRPD, Laser Flash Photolysis
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Quality Assurance, Regulatory, Compliance, FDA, GLP, auditing
Detail-oriented Chemist relocating to Long Island. More than ten years of experience. Excellent educational background complemented by work experience involving research in academia and industry. Career experience includes, method development with different analytical techniques in a GLP and GMP environment, method validation, product support, development and root cause investigation. A broad knowledge of chromatographic me...
I'd like to use my people and organization skills to communicate compliance requirements to cross-functional departments emphasizing the legal obligation biotech/pharma has to regulatory agencies and patients in an organization who supports the Quality Systems.
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Quality Control, Quality Assurance, Quality Auditor, Promotional, GCP GMP, Compliance Auditor
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Research Scientist, Microbiologist, Biochemist, Quality Analyst, Bio-science, Process Development
