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Clinical Regulatory Affairs Online Resumes
Director Corporate Compliance - Training, Communication & Policy
Ensure compliance at the federal, state and local levels, pertaining to Company's business operations and influence Company culture applying award winning ethics and compliance training and communication programs. Close collaboration with internal stakeholders to identify risk areas and resolve those issues.
Tags for this Online Resume: Compliance, Ethics, Training, Powerpoint, Excel , Word
Clinical Regulatory Affairs
Clinical Regulatory Affairs
Tags for this Online Resume: syracuse/rochester, material handler, operations, company driver, transporter, courier, courier/specimen
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 - 20 Years of Experience - Near 07417
Experienced regulatory professional with knowledge of FDA, EPA, USDA and international regulations for pharmaceuticals, chemicals, and food products. Demonstrated success in filing and securing regulatory approvals on time and within budget. Superior communication, interpersonal and organizational skills and demonstrated ability to work effectively with government regulators, outside laboratories and employees. Maintains...
Tags for this Online Resume: New Jersey, EPA/FIFRA/TCSA, FDA, multi-national experience, successful start-up, BS/MS/MBA, Compliance, Advertising, Government, Integrate, Summit, Budgeting, Licensing, Management
Clinical Regulatory Affairs - 20 Years of Experience - Near 08558
Regulatory Affairs Leader with demonstrated organizational and project management skills. Expertise in the development of product registrations, regulatory expertise in US Regulations, labeling and promotional materials for new and modified medical devices, over the counter drugs and cosmetics. Cross functional team player whom demonstrates effective communication & high level of details.
Tags for this Online Resume: 510 Submissions, Advertising , Labeling, Artwork review, Device Listings
Pharmacist - 10 Years of Experience - Near 60089
Tags for this Online Resume: Documentation, Regulatory Affairs, Audit, Clinical Research, Injections, Protocol, Research, Business Requirements, Focus, Medical
Clinical Regulatory Affairs - 20 Years of Experience - Near 53185
Quality Control/Position: Quality Control Technician
Tags for this Online Resume: Documentation, Product Design, Instrumentation, Pharmaceutical, Manufacturing, Project Leader, Compliance, ISO, Management, Marketing Management
Clinical Regulatory Affairs
Tags for this Online Resume: Report Writer (Toxicology), Quality Assurance, Preclinical Regulatory Affairs
Chief Operating Officer (Clinical and Regulatory) at CRO and Consulting company
COO or Vice President Clinical And Regulatory Affairs at small to medium Biotech/Pharma
Tags for this Online Resume: COO, Pharmaceutical , Biotechs, Clinical studies, Regulatory, NDA
Regulatory Affairs, Quality, and Clinical Evaluation Consultant to Medical Device Industry
PROFESSIONAL PROFILE: A focused, driven, and passionate regulatory affairs and quality/compliance/auditing consultant with hands-on experience in RA and Quality/Compliance/Auditing associated with activities which lead to, and maintain regulatory approval to ISO 13485, FDA 510 (k), EU CE Mark & other international market authorizations of medical device products and conformance/compliance of Quality Management Systems. Regu...
Tags for this Online Resume: Management, Regulatory Affairs, Assessments, Audit, Budgeting, ISO, Microsoft Office, Quality, Quality Assurance, Quality Management, oncology, protocol, 13485, FDA, 483, Warning Letter, Portuguese, Spanish, ANVISA, Lead Auditor, Quality Systems, Quality Audit, Medical Device
