| Distance: | Resume alert | Resumes 91 - 100 of 25453 |
Clinical Research Coordinator with Oncology Experience
Texas
... Identified, initiated, monitored and close out investigational sites in accordance with standard operating procedures (SOPs) and FDA guidelines. • Verified that the investigator and all research staff has adequate qualifications and resources and ... - Feb 05
... Identified, initiated, monitored and close out investigational sites in accordance with standard operating procedures (SOPs) and FDA guidelines. • Verified that the investigator and all research staff has adequate qualifications and resources and ... - Feb 05
Cert/PCEP QA Lead for Medical Devices & Cloud Systems
California
... Proven ability to design, execute, and manage comprehensive test plans in alignment with FDA (21 CFR Part 820) and ISO 13485 standards. Adept at collaborating with cross-functional teams, performing firmware and cloud-based application testing, and ... - Feb 05
... Proven ability to design, execute, and manage comprehensive test plans in alignment with FDA (21 CFR Part 820) and ISO 13485 standards. Adept at collaborating with cross-functional teams, performing firmware and cloud-based application testing, and ... - Feb 05
Regulatory Expert Global Medical Device Compliance
Sunnyvale, CA
... Core Competencies ● Global Market Access: Extensive experience spearheading submissions across major markets including the US (FDA), EU (MDR/IVDR), and Canada (Health Canada), as well as emerging markets in APAC, EMEA, and LATAM. ● Technical ... - Feb 05
... Core Competencies ● Global Market Access: Extensive experience spearheading submissions across major markets including the US (FDA), EU (MDR/IVDR), and Canada (Health Canada), as well as emerging markets in APAC, EMEA, and LATAM. ● Technical ... - Feb 05
Senior Manufacturing Leader, Lean & Compliance Expert
East Brunswick, NJ, 08816
... • Prepared and submitted over 30 regulatory submissions, including FDA 510(k) applications for Class I and II medical devices, ensuring compliance with 21 CFR Part 820 regulations. • Authored, reviewed, and approved Product Quality Complaint (PQC) ... - Feb 05
... • Prepared and submitted over 30 regulatory submissions, including FDA 510(k) applications for Class I and II medical devices, ensuring compliance with 21 CFR Part 820 regulations. • Authored, reviewed, and approved Product Quality Complaint (PQC) ... - Feb 05
Customer Service Oriented Pharmacy Assistant
Laurel, MD
... Food and Drug Administration (FDA) Silver Spring, MD August 2015– November 2018 Office Automation Clerk Used Microsoft Word to compose and edit standard documents, correspondence and emails for the Director, Program Management Office (PMO), Center ... - Feb 05
... Food and Drug Administration (FDA) Silver Spring, MD August 2015– November 2018 Office Automation Clerk Used Microsoft Word to compose and edit standard documents, correspondence and emails for the Director, Program Management Office (PMO), Center ... - Feb 05
Senior Scientist - Polymers, Materials & QC Leadership
White Oak, PA, 15131
... ●Provided training programs, staff educational in-services, safety leadership, health, environmental, including compliance and regulatory issues (i.e., FDA, OSHA, EPA) and updates to current and new employees. Additional Relevant Experience Sunoco ... - Feb 04
... ●Provided training programs, staff educational in-services, safety leadership, health, environmental, including compliance and regulatory issues (i.e., FDA, OSHA, EPA) and updates to current and new employees. Additional Relevant Experience Sunoco ... - Feb 04
Pharmacy-Safety and Clinical Research Specialist
Centreville, VA
... EXPERIENCE Oct 2017-JAN 2023 DRUG SAFETY SPECIALIST HealthCore [previously New England Research Institutes]-Watertown, MA Responsible for the review, evaluation and management of adverse event reports in accordance with FDA, EMEA, other applicable ... - Feb 04
... EXPERIENCE Oct 2017-JAN 2023 DRUG SAFETY SPECIALIST HealthCore [previously New England Research Institutes]-Watertown, MA Responsible for the review, evaluation and management of adverse event reports in accordance with FDA, EMEA, other applicable ... - Feb 04
Workday HCM Lead End-to-End Implementations Certified
Danbury, CT
... Participated in the setup of Shift Rules and Work Area assignments, addressing 24x7 manufacturing shift coverage and FDA audit compliance. Worked closely with HR and Operations to define Scheduling eligibility rules for lab technicians and clinical ... - Feb 04
... Participated in the setup of Shift Rules and Work Area assignments, addressing 24x7 manufacturing shift coverage and FDA audit compliance. Worked closely with HR and Operations to define Scheduling eligibility rules for lab technicians and clinical ... - Feb 04
Entrepreneurial Online Business Owner and Fundraising Specialist
San Pedro, CA
... Responsible for contacting and alerting pharmacies and consumers to DEA and FDA drug recalls. *Promoted from Executive Assistant. 6/88-7/90 LOGICON, INC. “ADMINISTRATIVE ASSISTANT” Prepared and compiled cost proposals and government contracts for ... - Feb 04
... Responsible for contacting and alerting pharmacies and consumers to DEA and FDA drug recalls. *Promoted from Executive Assistant. 6/88-7/90 LOGICON, INC. “ADMINISTRATIVE ASSISTANT” Prepared and compiled cost proposals and government contracts for ... - Feb 04
Operations Leader with 15 Years Production Experience
Eastman, GA
... planning (10+ years) • Trimming (cutting method) • Technical support • APIs • Help desk • Public speaking • Event sales • FDA regulations • Microsoft Word (9 years) • Sheet metal stamping • Materials handling • Custodial experience • Patient ... - Feb 04
... planning (10+ years) • Trimming (cutting method) • Technical support • APIs • Help desk • Public speaking • Event sales • FDA regulations • Microsoft Word (9 years) • Sheet metal stamping • Materials handling • Custodial experience • Patient ... - Feb 04