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Online Resumes with "Clinical Regulatory"
Clinical Regulatory Affairs - 4 Years of Experience - Near 02494
SUMMARY * Current graduate student working on second master's degree in Regulatory Affairs for acquiring general insights of regulatory profession and in-depth practical knowledge of regulatory compliance, including CMC (Chemistry, Manufacturing, and Controls) and quality system practices. * Extensive background in the biopharmaceutical industry and 3-year experience in upstream bench-scale cell culture process development ...
Tags for this Online Resume: Biopharmaceutical, Biotechnology, ICH, Regulatory Affairs, Manufacturing, Medical Devices, Regulatory Compliance, quality assurance, FDA, EU, Pharmaceutical, GMP
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
Pharmacist and Regulatory Affairs
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
Tags for this Online Resume: Product Development, ACD, Automatic Call Distribution, Data Management, Management, Budgeting, Infrastructure, Quality Assurance, Surgical, Test
Clinical Regulatory Affairs - 13 Years of Experience - Near 45208
SUMMARY Over 15 years industrial experience, with skills in pharmaceutical and beauty care industries, including expertise in areas such as FDA electronic product license applications, European regulatory affairs, consumer and product testing, and manufacturing compliance. I am a self-motivated creative team player, processing excellent interpersonal skills, strong leadership, communication and organizational abilities seek...
Tags for this Online Resume: Scheduling, Compliance, Mutual Recognition, Manufacturing, Procurement, Project Management, Project Manager, Regulatory Affairs, Management, Project Coordinator, European Experience, eCTD Publishing
Chief Operations Officer - 11 Years of Experience - Near 92122
SUMMARY of QUALIFICATIONS Available for remote project management and San Diego based roles leading business, clinical, compliance structures. Clinical and regulatory catalyst establishing organizational, technological and scientific intelligence, strategies and resources to ensure a profit based business and marketing environment. * Synergistic Scientific and Business acumen, proficient analytical, technical and interpreti...
Tags for this Online Resume: IVD/Medical Device, Pharmaceutical Research, RNA/DNA, Clinical Research, Operations, IND, Regulatory, Project Management, Oncology, AI, cNLP, Genomics
