| Resume alert | Resumes 81 - 90 of 245 |
Production Supervisor
Brownsburg, IN, 46112
... Complied at all times with SOX, USDA, FDA, DOT and U.S. Customs guidelines and regulations. Used item Numbers to properly stock warehouse. Attached identifying tags to containers. Adhered to all requirements and regulations for interstate HAZMAT ... - 2017 Nov 30
... Complied at all times with SOX, USDA, FDA, DOT and U.S. Customs guidelines and regulations. Used item Numbers to properly stock warehouse. Attached identifying tags to containers. Adhered to all requirements and regulations for interstate HAZMAT ... - 2017 Nov 30
Data Health
Indianapolis, IN
... Extract and analyze data from FDA approved package inserts for text mining to identify drug-drug interactions 2. Extract data from warehouse and produce reports for data analysis and data mining. 3. Customized NLP scripts to carryout data processing ... - 2017 Nov 08
... Extract and analyze data from FDA approved package inserts for text mining to identify drug-drug interactions 2. Extract data from warehouse and produce reports for data analysis and data mining. 3. Customized NLP scripts to carryout data processing ... - 2017 Nov 08
Data Microsoft Office
Indianapolis, IN
... Additional aspects included analyzing customer and data requirements, developing, generating, testing, validating, and documenting programs as well as ISS and ISE safety summary reports to meet FDA standards and submission including 21 CFR Part 11 ... - 2017 Oct 26
... Additional aspects included analyzing customer and data requirements, developing, generating, testing, validating, and documenting programs as well as ISS and ISE safety summary reports to meet FDA standards and submission including 21 CFR Part 11 ... - 2017 Oct 26
Project Management / Scrum
Indianapolis, IN
... Lead effort in 2017 FDA conversion of all nutrition fact panels to standards by bringing transparent project management through to printers, plant quality assurance, Purchasing, and Regulatory. Implemented feedback from category teams on product ... - 2017 Oct 24
... Lead effort in 2017 FDA conversion of all nutrition fact panels to standards by bringing transparent project management through to printers, plant quality assurance, Purchasing, and Regulatory. Implemented feedback from category teams on product ... - 2017 Oct 24
Global Clinical Trial Project Manager
Zionsville, IN, 46077
... Timeline development and risk assessment, vendor management, global trial planning & implementation, clinical trial reporting & close-out, FDA submissions, inspection readiness and support of an on-site, sponsor FDA inspection. • Strong knowledge of ... - 2017 Oct 12
... Timeline development and risk assessment, vendor management, global trial planning & implementation, clinical trial reporting & close-out, FDA submissions, inspection readiness and support of an on-site, sponsor FDA inspection. • Strong knowledge of ... - 2017 Oct 12
Administrative Professional, Data Entry, Accting, Customer Service
Fishers, IN
... •Maintain the clinical documents and drawings for FDA and Regulatory groups to ensure no deviations are committed and kept safe without any damage or deterioration with easy traceability. This may include various types of documents, including ... - 2017 Sep 27
... •Maintain the clinical documents and drawings for FDA and Regulatory groups to ensure no deviations are committed and kept safe without any damage or deterioration with easy traceability. This may include various types of documents, including ... - 2017 Sep 27
Manager Quality Control
Fishers, IN
... Proven record of accuracy and efficiency in facilitating operations while adhering to all regulatory standards (FDA, CDC). Broad understanding of cross-functional roles, including counseling, data control and special donations. ORGANIZATION AND ... - 2017 Sep 05
... Proven record of accuracy and efficiency in facilitating operations while adhering to all regulatory standards (FDA, CDC). Broad understanding of cross-functional roles, including counseling, data control and special donations. ORGANIZATION AND ... - 2017 Sep 05
Project Management
Indianapolis, IN
... Serve as a subject matter expert on FDA and OSHA regulations, policies, and procedures. Utilize process improvement and project management tools to evaluate manufacturing operations and efficiency. PROFESSIONAL EXPERIENCE Vesta Pharmaceuticals Inc. ... - 2017 Aug 18
... Serve as a subject matter expert on FDA and OSHA regulations, policies, and procedures. Utilize process improvement and project management tools to evaluate manufacturing operations and efficiency. PROFESSIONAL EXPERIENCE Vesta Pharmaceuticals Inc. ... - 2017 Aug 18
Project Coordinator
Indianapolis, IN
... This included electrical, daily updates, scheduling forward, ensuring project scheduling standards, and compliance with Lilly/FDA policies and standards Coordinated with Senior Project Planner on any schedule changes and incorporating those changes ... - 2017 Aug 13
... This included electrical, daily updates, scheduling forward, ensuring project scheduling standards, and compliance with Lilly/FDA policies and standards Coordinated with Senior Project Planner on any schedule changes and incorporating those changes ... - 2017 Aug 13
State University Professional Experience
Greenfield, IN, 46140
... Have working knowledge of safety and risk assessment, Food and Drug Administration (FDA) regulations, current Good Laboratory, Clinical and Manufacturing Practices (GLP GCP and GMP). Primary responsibilities include: designing studies, performing ... - 2017 Jul 30
... Have working knowledge of safety and risk assessment, Food and Drug Administration (FDA) regulations, current Good Laboratory, Clinical and Manufacturing Practices (GLP GCP and GMP). Primary responsibilities include: designing studies, performing ... - 2017 Jul 30