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Resume alert |
Resumes 11 - 20 of 92 |
Connecticut
... Solving • Strong Work Ethic • Fluent in English and Spanish • Strong Organizational and Time Management Skills • Coordinating clinical trials conducted by a supervising Principal Investigator in accordance with FDA, GCP and protocol guidelines. ...
- 2023 Oct 12
Waterbury, CT
... * Prepare and serve clients nutritious meals approved by FDA. *Clean and sanitize the facility. EDUCATION 1998-1999 Bachelor in Human Services Audrey Cohen College New York, New York, United States • Human Services WORK AUTHORIZATION I am authorized ...
- 2023 Oct 02
New Haven, CT
... 2 days Capacity Building of Staff of HEIs/HEC training May 22-23,2015 FDA training for Project wining, COMSATS Institute of Information Technology Chak Shehzad Campus 2016. 5 days training of English medium use in class, COMSATS Institute of ...
- 2023 Sep 24
Durham, CT, 06422
... Molecular Biology Analysis skills Microbiology Calibration Clinical Research Clinical Trials Quality Management Leadership CGMP FDA Regulations Company safety Coordinator Research & Development ISO 9001 Product Development Laboratory Management ...
- 2023 Sep 07
Hamden, CT
... Conducted clinical screening processes per company procedures and FDA guidelines. Extensive knowledge of health plans including familiarity with prior authorization and precertification processes. Worked on problems of a diverse scope where analysis ...
- 2023 Aug 14
Waterbury, CT
... Familiar with FDA, TS14001, ISO9000 AS9100 and Nadcap preparing for, auditing throughout process, and maintaining certificate. All aspects GMPs and GLPs. Hands on optimizing and maintaining analytical instruments such as IR, GC, HPLC, AA, XRF and ...
- 2023 Jun 01
Fairfield, CT
... Quality / Regulatory Affairs Professional Experience and direction allowing companies to build the required Quality Management process to meet FDA quality compliance regulations. Broad Quality Assurance and Compliance experience in the medical ...
- 2022 Dec 14
Naugatuck, CT, 06770
... Participated in successful remediation program for FDA Warning Letters/Critical 483’s that brought the site into compliance. The program led to removal of the Warning Letter and approval of new commercial products. Performed scale-up and process ...
- 2022 Oct 04
Fairfield, CT
... Resume 3/5 blood brain barrier as well as the lymphatic system • Established CRO partnerships with Wuxi Biologics, BioAgylitics, and Invicro • Advanced pre-clinical brain metastases program to readiness for an FDA regulatory meeting • Assumed ...
- 2022 Aug 01
Trumbull, CT, 06611
... Indicators (KPI’s), material inventory, sales and stales, budget for each launch • Manage legal compliance with FDA, EU, Cuba, Canada, Haiti and Local Regulations • Manage information systems, formulas and material master data (SAP PP Module). ...
- 2022 Jul 14