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Resumes 1 - 10 of 245 |
Fishers, IN
... ● Configuration Management ● Information Technology ● Medical Terminology ● Process Improvement ● HIPPA Compliance 510K FDA submissions ● Medical Device Registration ● Clinical Evaluation Report Writing ● Quality Management System EXPERIENCE ...
- May 13
Indianapolis, IN
... Worked alongside quality control experts to meet customer expectations and FDA regulations. · Thoroughly reviewed and approved all documentation and reports before product release. Trainer Sld of ADIDAS group - Indianapolis, IN September 2002 to ...
- May 11
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
Bargersville, IN
... ●Appeared before the FDA, BMA, and European regulatory agency to answer all questions regarding the phase 1,2,3 plans and protocols, ●CP&P on cross-functional drug development teams, contributed to design drug development strategies, regulatory ...
- Feb 12
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