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Chicago, IL
... • Maintain accurate documentation and ensure compliance with HIPAA and FDA reporting standards. • Support new product launches, process changes, and mentor junior team members. Senior Medical Associate at Northwestern Memorial Hospital, Chicago ...
- Jun 12
Hillsboro, OR
... Proven expertise in authoring FDA submissions, SOPs, verification reports, and scientific literature across oncology, molecular biology, and gene therapies. Adept at distilling complex scientific data into clear, concise documents for both technical ...
- Jun 12
Kenosha, WI, 53140
... Staff Training Microsoft Applications SAP ComplianceWire Career Highlights Optimized quality assurance and regulatory compliance frameworks, ensuring seamless adherence to FDA, EMA, and internal audit standards with zero critical findings. ...
- Jun 12
Bowie, MD
... Job Title: Diverse HHS & DoD Portfolio Contracts Manager Woodlawn, MD (February 2021– June 2021) Northrop Grumman Systems Corporation – Health Information Technology Job Title: CMS, NIH, FDA, SSA Contracts Manager Woodlawn, MD (Oct 2016 – January ...
- Jun 12
Raleigh, NC, 27610
... for audits by governing bodies (FDA, MHRA) ●Read, write and edit methods, protocols and SOPs ●Mentor/Train new and junior employees ●Technical Quality review of data and documentation (ALCOA+, denoting Out Of Specification and Out Of Trend data; ...
- Jun 12
Albuquerque, NM
... Professional Experience Sartorius Bioanalytical Instruments, Inc., Albuquerque, NM Software QA Manager/Scrum Master Mar 2019 - Sep 2024 Led 3 QA engineers in testing data control/acquisition software for FDA-regulated medical devices (iQue Flow ...
- Jun 11
Tucson, AZ
... they are about my ow n personal experience), except those stated in materials published by Herbalife Nutrition, or use the name of the Food and Drug Administration (FDA) or any other regulatory agency w hen representing Herbalife Nutrition products. ...
- Jun 11
Fort Worth, TX
... Ensured the company is always in compliance with the DEA, FDA, EPA, and OSHA. Assisted outside sales force and customers with questions regarding DEA and Board of Pharmacy regulations. Consistently improved production and accuracy by providing ...
- Jun 11
Phoenix, AZ
... oversaw and led 4-6 moderately complex Companion Diagnostic (CDx) clinical cancer trial projects comprised of both internal teams and external stakeholders (Pharmaceutical companies and the FDA), some full life cycle, some post kick-off. Accountable ...
- Jun 11
United States
... Strong command over the IT-regulated work environment FDA, GXP process compliance for Medical and pharmaceutical testing. Have experienced in both technical and functional upgrade of the project. Compared the two systems for adjustment in dictionary ...
- Jun 11