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Online Resumes with "Medical Device Reporting"

Pharmacovigilance, San Antonio, Tx

Bring my expertise in pharmacovigilance and regulatory complaince for pharceutical or medical device products.

Tags for this Online Resume: Registered Nurse, Postmarketing Safety, Medical Device Reporting, pharmaceutical safety, pharmacovigilance, FDA compliance

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Public policy research--20 years

Conduct and direct public policy research, especially in the health care field

Ideal Companies: govt or govt contractors.

Tags for this Online Resume: statistics, research, management, public presentation, relocate anywhere, public policy, statistics/computers, SQLserver. SPSS, SASS

Over 20 years working experience with Quality Management Systems, with oversight of documentation and records control, corrective and preventive actions (CAPA), quality and regulatory monitoring over design controls, risk management and change control. O

Work within the overall quality management system of the organization providing quality and regulatory compliance suppport and feedback.

Tags for this Online Resume: quality specialist, risk management, change control, documentation control, corrective and preventive actions (CAPA), bilingual

Clinical Nurse Analyst Product Safety and Perfomance

Dedicated and motivated healthcare professional with over 13 years of relevant clinical training and expertise in Perioperative Nursing seeking a position into the Medical Device Industry. Offer a solid foundation in pharmaceuticals, surgical procedures, and healthcare advancements. Working knowledge of medical device complaint handling/analysis with familiarity with Medical Device Reporting and Vigilance per FDA, ISO, QSR,...

Clinical Research Associate

To obtain a Clinical Research Position in the Minnesota Area.

Tags for this Online Resume: Knowledge of 21 CFR, Quality System Regulation (QSR), Medical Device Reporting, Regulatory Compliance , Regulatory Submissions , ICH GCP Guidelines


High quality in laboratory, clinic, data, clinical trials.

Tags for this Online Resume: medical laboratory, CRA, clinical trials, Medical Device Reporting

Not Listed - 20 Years of Experience - Near 91740

SUMMARY An analytical and detail-oriented healthcare professional, with extensive experience in nursing, biotechnology, regulatory compliance, global safety, pre- and post-market studies, research and development, clinical trials and FDA compliance. Utilizes exceptional organization and communication skills to consistently set and meet high-quality standards. Possesses a proven ability to utilize a cross-functional skill se...

Tags for this Online Resume: Complaints, Coding, Compliance, Manufacturing, Medical, Oncology, Pharmaceutical, Policies and Procedures, Quality, Quality Assurance

Medical Device Specialist/Coordinator/Reporting - 4 Years of Experience - Near 94087

PROFESSIONAL SUMMARY * Exceptional leadership and motivational skills * Team player with a diverse range of work and cultural experience * Strong analytical and quantitative skills with great attention to detail * Experience Medical Device reporting/ Quality assurance/ Regulatory affairs.

Tags for this Online Resume: Quality, Complaints, Documentation, Inventory, Inventory management, Management, MDR, Medical, POS, physical therapist, physical therapy, outpatient physical therapy, outpatient rehabilitation, nurse, registered nurse, care, rn, pt, medi

Manager - 10 Years of Experience - Near 75057

Detail-oriented and hardworking individual with more than 20 years of experience in the Medical Device industry. Highly qualified in Complaint Handling Medical Device Reporting and Post Market Surveillance functions.

Tags for this Online Resume: Administrative Assistant, Call Center Management, Management, Microsoft, Microsoft Excel, medical device, CAPA, complaints, MDR reporting, quality systems, quality audits, data analysis, post market surveillance

Quality Coordinator - 0 Years of Experience

Summary: * Extensive experience in clinical data management, pharmaceutical, and device research industries. * Experience working with Adverse Event Reporting and Medical Device Reporting. * Strong analytical, problem resolution, and project management skills. * Proficient in monitoring and managing record retention timelines for all clinical and regulatory documents and assistance in the preparation and review of documents...

Tags for this Online Resume: Data Entry, Database, Distribution, Filing, Documentation, Licensing, Medical, Microsoft Access, Regulatory Affairs, Research, clinical research