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Complaints Quality Engineer II

JBL Resources  –  Elkton, MD, 21921
... Ensuring all complaint handling processes comply with relevant regulatory requirements (e.g., FDA, ISO) and internal quality management systems. Staying current with industry standards and regulations. Contributing to continuous improvement ... - Sep 07

In-Store Shopper - Part Time Seasonal

Whole Foods Market  –  Thornbury Township, PA, 19342
... Exposure to FDA approved cleaning chemicals. Exposure to temperatures: <32 degrees Fahrenheit (freezing), 32-40 degrees Fahrenheit (refrigerators), >90 degrees Fahrenheit. Ability to work a flexible schedule including nights, weekends, and holidays ... - Sep 20

US Medical Head - Immunology

AstraZeneca  –  Delaware Avenue, DE, 19806
... The Medical Head is knowledgeable of the actions of regulatory bodies, in particular FDA, and has experience with clinical trials. An ideal candidate should have significant experience in immunology and would thrive on proactively engaging internal ... - Sep 10

Compliance Engineer Sr., EUMDR

JBL Resources  –  Elkton, MD, 21921
... Practical experience with FDA, ISO 13485, EU MDR, MDSAP and global quality system requirements, preferably for medical devices. Ability to use process development tools (ex. Lean Six Sigma) Ability to apply a practical level of statistics. Ability ... - Sep 07

Clinic Pharmacist

ChristianaCare  –  Elkton, MD, 21920
... utilization Participate in reporting ADEs to institutional committees and national programs (e.g., the FDA MedWatch program) Participate in identifying and submitting events via Report2Learn (R2L) system and providing follow up assessment. ... - Sep 16

Plant Manager

STERIS Corporation  –  Sharon Hill, PA, 19079
... Regulatory/FDA, medical device operations experience, strongly preferred. Experience with MRP/Kanban environment, preferred. What STERIS offers you We value our employees and are committed to providing a comprehensive benefits package that supports ... - Sep 13

Medical Assistant

Penn Medicine  –  Kennett Square, PA
... Other / Regulatory: + Ensures compliance with all applicable federal, state, and local regulatory standards (ex TJC, DOH, FDA, HIPAA, HCFA, DPW, LCGME, SCGME, etc.) + Flexible and readily adopts new processes and engages in practice operation ... - Sep 06

Clinical Research Coordinator

The Nemours Foundation  –  Wilmington, DE
... responds to sponsor queries, prepares for audits by sponsor, IRB and/or the FDA/DHHS. 10. Participates in continuous process improvement initiatives and implementation of outcomes 11. Prepares for internal and external audits. Prepares corrective ... - Aug 31

Clinical Research Coordinator

The Nemours Foundation  –  Wilmington, DE
... responds to sponsor queries, prepares for audits by sponsor, IRB and/or the FDA/DHHS. Participates in continuous process improvement initiatives and implementation of outcomes Prepares for internal and external audits. Prepares corrective action ... - Aug 31

Clinical Research Coordinator

The Nemours Foundation  –  Wilmington, DE
... responds to sponsor queries, prepares for audits by sponsor, IRB and/or the FDA/DHHS. 11. Attendance at and participation in relevant clinical divisional/departmental activities to assure routine administrative procedures are followed. Further ... - Sep 18
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