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Indianapolis, IN
... I also did a contract job through craft Mark bakery which gave me experience dealing with food and the FDA in the manufacturing field. So I’m well rounded in the field. I also managed a kid salon called shear fun a few days a week after I received ...
- Apr 15
Indianapolis, IN
... Use of microscope to inspect various points of mentioned device to meet FDA requirements. Ryder, Whitestown, IN 2014/ 2017 Team Lead Responsible for all properly audited orders being scanned, packed, and shipped in our highest volume area. Also ...
- Mar 25
Indianapolis, IN
... Regulatory and compliance - Oversight of FDA requirements for new product registrations, packaging requirements and GMP practices. Tracking and maintenance of records. Project Management - End-to-end process oversight, including manufacturing ...
- Mar 06
Mooresville, IN
... 10 national meeting in Washington DC Appointments FDA Pharmacy Compounding Advisory Committee Appointed 2020 – present as voting member. Review information and materials for potential APIs to be added to the national compounding list. 856 IAC 1-30 ...
- Feb 16
Plainfield, IN
... HIPAA • August 2016 - May 2019 Advocate new quality and procedures as nessary to ensure high • quality grade poultry • Follow FDA standards & precautions • Control poultry temperature & ensure plant is sanitized Conduct meeting with FDA to ensure we ...
- Feb 13
Indianapolis, IN
... ● Data Entry, 10-Key and Customer Service Skills, etc ● Discard specimen material no longer needed per assays and test study results ● Assist FDA with audits conducted ● Use of GMP, GDP and GLP practices - Good Manufacturing, Good Documentation, ...
- Feb 09
Indianapolis, IN
... agendas • Reporting for employee salaries and benefit packages • Review and approve customer billing and credit issues • Complete employee handbook revisions, facility evacuation maps, Emergency Action Procedures, DOT and FDA site review forms; ...
- Feb 09
Indianapolis, IN
... Roche Diagnostics (formerly Boehringer Mannheim) industry leader in medical devices in manufacturing Vitro diagnostics FDA regulated company. Always willing to work overtime. Consistently complete work accurately and on time. Willing to relocate: ...
- Jan 06
Lebanon, IN
... ●Prepare bulk quantities of product while adhering to FDA regulations and GMP’s. ●Prepare ingredients for all products required for the production day. ●Maintain process environment by following safety, health, environmental standards and procedures ...
- 2023 Dec 26
Indianapolis, IN
... software validation program and 10-point hardware validation program as required by FDA (40 hours each week for 4 months) Eli Lilly and Co., Indianapolis, In., diagramming the scientific development of drugs (80 hours total) Polaroid ID Systems, Ft. ...
- 2023 Nov 26