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Resume alert |
Resumes 11 - 20 of 59 |
Greer, SC
... Directed efforts to be compliant with FDA regulations regarding employee competency & training, recordkeeping & training effectiveness. Implemented Pay for Performance (PP) plan for Liquid and Nicogen manufacturing operations Recruits, interviews, ...
- 2023 Sep 11
Greenville, SC, 29607
... 10/2014 – 8/2015 – US Food & Drug Administration Clinical Trails Reports Repository – Richmond, VA - (Remote & Onsite) UX/UI Interface Lead Designer, Contributing Developer Designed the new dashboard interface for FDA’s “Clinical Trials Repository”. ...
- 2023 Sep 05
Simpsonville, SC
... Lean and visual factory, process validations, supply chain, MRB/DRB, CAPA management, package / ship process development, and Document Control in an FDA Regulated industry (ISO-13485). Impact: Developed QMS for startup organization including ISO ...
- 2023 Aug 01
Pelzer, SC
... which required calibrations and validation ●Maintained and Directed other Technicians in performing Calibration program per company, FDA and NIST directives while developing SOP(standard operating procedures) equipment policies and critical controls ...
- 2023 Mar 12
Greer, SC
... Accountable for accurate packaging of products free from contamination in accordance with FDA cGMP requirements. Setup filler. Correctly document downtime in batch record. Operate material handling equipment. Review completed batch records for ...
- 2023 Mar 01
Greenville, SC
... Responsibilities include, but not limited to: The operation of chemical reactors under "GMP" (Good Manufacturing practice guildelines) Also in accordance with FDA guidelines, using "OIT", computer system to operate automated equipment. Maintaining ...
- 2023 Feb 20
Simpsonville, SC
... Implement and Oversee ISO 9000/2000 Certification, GMP Quality System, FDA Regulations and Medical Device Manufacturing Regulations, 21CFR 820 Quality System, Sterilization Process and Regulations for Gamma Radiation and ETO Gas. Train personnel in ...
- 2022 Nov 15
Greer, SC
... Held knowledge of cGMPs, FDA and DEA guidelines, applying them effectively. Boddie Noell Supervisor 9/2000 to 1/2014 Knightdale NC Full Time Worked as the supervisor for a reputable company, providing all team members with the necessary information ...
- 2021 Aug 06
Greenville, SC, 29601
... Kazan, Root Cause Analysis, Arc Flash/Electrical safe work practice OSHA standards Continuous Improvement (CI) Processes, GMP FDA USDA AMI Medical Device Hygienic Engineering, Incident Investigation, ISO Standards, Lean Manufacturing technique OEE ...
- 2021 Jul 05
Easley, SC, 29642
... QC, Quality, Safety, GMP, FDA, Experience Senior Designer 9/2020 – Present LTF Design Piping design, Fabrication and Checking, work performed in W2 format for various clients such as MEP-3, Novo Nordisk and Tesla. Microsoft products, Autodesk ...
- 2021 Jun 29