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Resume alert |
Resumes 21 - 30 of 456 |
Cary, NC
... Monitors FDA and manufacturer updates for material changes to drug inventory, including but not limited to, recalls, black box warnings, new drugs to the market and brand to generic change. Process pharmacy appeals, interpreting member and provider ...
- 2023 Dec 15
Durham, NC
... Proficient in data entry and drug safety database (ARGUS) Knowledge of different therapeutic areas- Respiratory/Infectious/Cardiovascular Understanding of FDA and international regulations. Familiar with the use of search engines like PubMed, EMBASE ...
- 2023 Dec 12
Durham, NC
... •Identify potential Adverse Event situations for reporting to Pharmacovigilance ensuring AbbVie meets FDA regulations. Duke University Health Systems (PRMO), Durham, NC April 2021 – September 2022 Patient Account Associate Authorization Denials ...
- 2023 Dec 08
Raleigh, NC, 27603
... Developed requirements for FDA-compliant hardware infrastructure. Managed and enforced network and software security. Performed regular vulnerability tests, penetration tests, and threat assessments. Supported 4,000 users and developed, validated, ...
- 2023 Nov 27
Wendell, NC
... • Ensured that beer produced met FDA requirements by being packaged properly and safely for distribution to customers. • Operated and maintained packaging equipment and troubleshooting problems that arose during our packaging process, while ...
- 2023 Nov 24
Garner, NC
... Adherence to FDA, GMP, cGMP, ISO 9001: 2015, ISO 13485:2016, ISO 14971, PPE EU 2016/425, CE, AS9100, FAI, and ASTM standards, along with the proficiency in Minitab, PowerBI, AutoCAD, SolidWorks, Track Wise, SAP, Veeva, and the Eastman S125 CMM ...
- 2023 Nov 10
Durham, NC
... This position was responsible for facilitating the timely completion of FDA Regulated Updates Worked closely with Product Support Teams/Business Units and Data Management Teams to ensure install base accuracy and data integrity for FDA Compliance ...
- 2023 Nov 01
Raleigh, NC
... Management, Systems Development, Validation Management, Test Management and Integration Management as well as experience with FDA 21 CFR parts 11/210/211/820 GMP/non-GMP documentation, FDA Consent Decree, Vendor Audits(GMP,GxP,GCP) Highly skilled in ...
- 2023 Oct 10
Willow Spring, NC
... Worked on team developing a new product line Biogen 2004-2005 Durham, NC Manufacturing Associate I Executed manufacturing process steps using standard operating procedures Monitored bioreactors and sampled product for quality and FDA conformity. ...
- 2023 Oct 02
Cary, NC
... ·Extensive experience in testing clinical and pharmaceutical applications ·Extensive knowledge of 21 Code of Federal Regulations (21 CFR Part 11., 210, 211 and 820), FDA, and GxP’s(GDP, GMP, GLP and GCP) including electronic records, electronic ...
- 2023 Sep 21