| Resume alert | Resumes 1 - 6 of 6 |
Medical Device Technical Writing. Investigations
Arecibo, Puerto Rico, 00612
... Proven as highly responsible, analytical, a "right the first time" mindset and results oriented with strong leadership skills – Documentation Lead, Manufacturing GMP Coordinator, QE Inspector Supervisor, QA Manager, CAPA Lead, Sr. QA Specialist. ... - Jan 10
... Proven as highly responsible, analytical, a "right the first time" mindset and results oriented with strong leadership skills – Documentation Lead, Manufacturing GMP Coordinator, QE Inspector Supervisor, QA Manager, CAPA Lead, Sr. QA Specialist. ... - Jan 10
Scientist, Chemist, Material Sientist, Analytical Development, QC, R&
Mayaguez, 00682, Puerto Rico
... Subject matter expert in all classes of laboratory non-conformance investigations like out of specifications (oos), out of trending (oot), and GMP auditing . Subject matter expert in manufacturing incidents control including generating FDA 483 ... - 2021 Jun 06
... Subject matter expert in all classes of laboratory non-conformance investigations like out of specifications (oos), out of trending (oot), and GMP auditing . Subject matter expert in manufacturing incidents control including generating FDA 483 ... - 2021 Jun 06
Quality Operator
Aguadilla, PR
... ●Maintain compliance with GMP and all local/federal regulations. ●Documents on forms in accordance to Good Documentation Practices ●Performs a variety of in-process product inspection to assure product quality Responsible for all activities to ... - 2018 Jul 26
... ●Maintain compliance with GMP and all local/federal regulations. ●Documents on forms in accordance to Good Documentation Practices ●Performs a variety of in-process product inspection to assure product quality Responsible for all activities to ... - 2018 Jul 26
Management Quality
Aguadilla, Puerto Rico
... 00603-9375 787-***-**** / acuysn@r.postjobfree.com Professional Summary Professional with experience in CAPA, Change Control, Cross-functional Team Leadership, FDA, GMP, Regulatory Requirements, Root Cause Analysis, Technical Writing, Technology ... - 2016 May 26
... 00603-9375 787-***-**** / acuysn@r.postjobfree.com Professional Summary Professional with experience in CAPA, Change Control, Cross-functional Team Leadership, FDA, GMP, Regulatory Requirements, Root Cause Analysis, Technical Writing, Technology ... - 2016 May 26
Technician Medical Device
Isabela, PR, 00662
... • Knowledge in GMP, SOP, FDA, EHS, and LOTO and other documentation and process form. • Troubleshoot by using drawing, plc or other software method. • Excellent in promoting team work. • Keep all production information in SCADA application. • Always ... - 2010 Oct 17
... • Knowledge in GMP, SOP, FDA, EHS, and LOTO and other documentation and process form. • Troubleshoot by using drawing, plc or other software method. • Excellent in promoting team work. • Keep all production information in SCADA application. • Always ... - 2010 Oct 17
Ingeniera Industrial
Aguada, PR, 00602
... among employees, art crafts, write poems Computer literate: Word, Excel, Power Point, C, AutoCAD, Math Cad, Mat lab, Mini tab, PLC, Direct Soft, Wonder Ware, Visio and knowledge in FDA, SOP, GMP’s, GDP’s References Available upon request - 2009 Oct 02
... among employees, art crafts, write poems Computer literate: Word, Excel, Power Point, C, AutoCAD, Math Cad, Mat lab, Mini tab, PLC, Direct Soft, Wonder Ware, Visio and knowledge in FDA, SOP, GMP’s, GDP’s References Available upon request - 2009 Oct 02