| Distance: |
Resume alert |
Resumes 401 - 410 of 25478 |
Mumbai, Maharashtra, India
... 2015 FDA Approval in Liquid oral. WORK EXPERIENCE: Total Work Experience: 18+ years 7. Livealth biopharma pvt. ltd, Mahape Assistant manager- Production planning. From (may.2020 to till date) 1.Searching suitable manufacturing sites for export ...
- 2025 Sep 09
Studio City, CA
... Presided over development and implementation of clinical resources and tools in accordance with industry best practices and FDA guidelines. Significantly contributed towards FDA and HRSA submissions by formulating detailed reports outlining adverse ...
- 2025 Sep 09
Sandviken, Gavleborg, 811 33, Sweden
... Louis, MO 63110 Clinical Research Specialist (hybrid) Jan 2020 – Nov 2021 Subject matter expert in regulatory submissions and project management (Single patient compassionate treatment submission to FDA, industry sponsored studies, secondary ...
- 2025 Sep 08
Mukwonago, WI
... Responsible for the successful turnarounds to improve profit margins in supply chain, purchasing and project management in the supply base in multiple OEM and Tier 1 settings as well as FDA requirements and processes. Extensive experience with low ...
- 2025 Sep 08
East Providence, RI
W Vincent Wang Cell: 781-***-**** • E-mail: *******.******@*****.*** • E Providence, RI 02914 CORE SKILLS: Chief Representative of company on ISO9001, IATF/ISO 16949, 21CFR/FDA, ISO13485, ISO14971, cGMP, ISO14001, OSHA & QA/QC. Established ISO 9001 ...
- 2025 Sep 08
Upper Marlboro, MD
... Perform Software testing involving both manual testing for Web and Client/ Server applications for Animal Drugs at FDA. Directly Interact with Developers, Business Analysts and Clients for Test requirements, clarifications and Testing. Provide daily ...
- 2025 Sep 08
The Villages, FL, 32162
... Design Labeling Engineer FDA contractor Medtronic, Google, Johnson+Johnson, 2017-2023 Senior Technical Writer Oracle, Minneapolis, MN 01/05 - 01/16 Managed executive scheduling, travel arrangements, and daily task prioritization. Assisted leadership ...
- 2025 Sep 08
Newark, NJ
... • Knowledge of cGMP/FDA regulated industry
- 2025 Sep 08
Corona, CA
... Experience in regulatory environment, FDA compliance. Datacenter management and consolidation. Good knowledge of TCP/IP, OSI networking models and routing protocols. Experience implementing network security, active directory security hardening, ...
- 2025 Sep 07
Lowell, MA
... Researched FDA websites, printed documents, emailed to requesting individuals. Contact person for department; interfaced with parent company representatives. Contacted German headquarters for inquiries, sent FedEx packages, scheduled meetings. ...
- 2025 Sep 07