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Browse Online Resumes by Occupation
Science & Biotech Online Resumes
Study Coordinator
Summary Study Coordinator with 6 years' experience specializing in technical support of animal studies requiring GLP compliant interpretations, analysis, documentation, and reporting of results per FDA regulations beginning with protocol development support and creation of shell reports resulting in a Final product ready for FDA Regulatory Filings. Areas of Expertise / Core Competencies * Highly dependable, focused and dete...
Tags for this Online Resume: Documentation, Good Laboratory Practices, Protocol, Analytical Skills, Biomedical Industry, Quality, Quality Assurance, Coordinator, Medical Devices, Regulatory
Clinical Regulatory Affairs
Summary of Qualifications * Coordination of CTA filings and Marketing Authorization Applications in rest of world countries * Strong leadership skills with proven results in making authoritative business decisions, executing decisions, and accounting for results,
Tags for this Online Resume: Manufacturing, Management, Documentation, Consulting, Applications, Clinical Research, Pharmaceutical, Process Improvements, Project Management, Protocol
Clinical Regulatory Affairs - 4 Years of Experience - Near 55434
SUMMARY OF QUALIFICATIONS: An adaptive and highly organized professional seeking a challenging opportunity in the IT space. Experienced change agent, constant problem solver, always watching for process automation and improvement opportunities on behalf of her clients. High learning curve Analytical for technical systems software mechanical and electrical Teamwork Goal Setting and Team Empowerment
Tags for this Online Resume: Documentation, Technical Writing, Packaging, Pharmaceutical, Process Improvement, SAP, User Documentation, Adobe, Adobe Illustrator, Audit
Clinical Regulatory Affairs - 4 Years of Experience - Near 44321
CAREER SUMMARY: An experienced Quality Specialist with a strong background in Technical Writing, Quality Auditing and Complaint Handling. Experienced in medical devices, pharmaceutical manufacturing and pre-clinical testing environment. Recognized as a Quality Assurance Top Performer and as a Cross-Functional Departmental Trainer.
Tags for this Online Resume: Audit, Documentation, Manufacturing, Policies and Procedures, Quality, Quality Assurance, Assessments, Complaints, Corrective Actions, Akron
Clinical Regulatory Affairs - 3 Years of Experience - Near 95112
Detail-oriented dedicated team player with strong regulatory & management skills focused in Biomedical/Biotechnology industries. Seeking new opportunitites in Biomedical/Biotechnology industries.
Tags for this Online Resume: Audit, Biotechnology, Management, Research, Bengali Language, C Programming Language, Complaints, Compliance, DBMS, Dialysis
Clinical Regulatory Affairs - 2 Years of Experience - Near 21075
Tags for this Online Resume: Clinical Research, ELISA, Equity, Management, Microsoft, Microsoft Access, Microsoft Office, Microsoft Windows, Operating Systems, Public Health
Clinical Regulatory Affairs
Over 25 years of experience in Drug Regulatory Affairs pharmaceutical development and registration with a thorough working knowledge of FDA regulations and requirements related the pharmaceutical industry emphasis on Chemistry Manufacturing and
Tags for this Online Resume: Gateway, Project Leader, Spl (HP-Sys Asmblr Lang), Regulatory Affairs, Integrate, Assessments, Integrated Development Environments, Microsoft Word, Word Processing, Manufacturing
Clinical Regulatory Affairs
SUMMARY Professional with over twenty five years of broad-based experience in risk management ensuring that the health and safety of employees, the public, and the environment are maintained to the strictest of standards by taking a proactive, rigorous, value-added approach employing strategic vision and innovation while practicing fiscal stewardship. Undertakings include laboratory, facility and manufacturing regulatory co...
Tags for this Online Resume: ISO, Management, Program Manager, Quality, Quality Assurance, Quality Management, Manufacturing, Risk Management, Distribution, Integrate, Root Cause, Compliance, Corrective Action, Safety, Environmental, 14001, Team, EHS, GMP, Laboratory, Leader, Pharmaceutical, Biotech, due diligence
Clinical Regulatory Affairs - 2 Years of Experience - Near 02120
Tags for this Online Resume: Database, Documentation, Applications, Audit, Audit Compliance, Coding, Complaints handling, Compliance, Data Entry, Drug safety, Pharmacovigilance, Medical devices, Regulatory Affairs, Medical terminology, Pharmacology, Dentist, Regulatory reporting, MDR
Clinical Regulatory Affairs - 17 Years of Experience - Near 30024
Tags for this Online Resume: regulatory affairs, clinical coordinator, atlanta, Quality Assurance, documentation, time management, orginazation
Not Listed - 8 Years of Experience - Near 27709
QUALIFICATION SUMMARY * Excellence in customer service * Strong oral and written communication skills with customers and colleagues * Demonstrated ability to manage multiple projects * Dedicated and resourceful team member * Documentation Management/Documentum * Inventory Control * Testing/Validation/Rosetta eCTD * Auditing/FDA Audits
Tags for this Online Resume: Imaging, Management, ANSI, Ansi (Am Natl Stds Inst), Audit, Communication Skills, Customer Service, Data Entry, Distribution, Document Management
Clinical Regulatory Affairs
Tags for this Online Resume: Product Development, ACD, Automatic Call Distribution, Data Management, Management, Budgeting, Infrastructure, Quality Assurance, Surgical, Test
