Process Engineer (Auburn, AL) F/T. Executes numerous functions w/in an ISO 13485 registered Quality Mgmt System. Responsible for QA activities involving a variety of different products, assemblies, & components using various mfg & assembly processes as related to a medical device contract mfg. Perform advanced quality planning functions, incl Gage R&R & MSA, drawing reviews, capability studies, production documentation approval, inspection plans. Perform Statistical Analysis, incl SPC, ANOVA, T-Test, F-Test, capability studies. Lead pFMEA sessions & lend support for dFMEA meetings. Author Level 2 & Level 3 SOPs & Work Instructions. Responsible for QMS documentation review & mgmt (Device Master Records, Device History Records, CAPA & Complaint system). Bach's deg in Industrial Engg, or Industrial & Systems Engg, or closely related field plus 24 months of exp in job offered or as Industrial Engineer, Mfg Process Engineer, Plant Engineer, Industrial Process Engineer or closely related reqd. Email resume to: SiO2 Medical Products, Inc. (dba: SiO2 Materials Science), Attn: Meesha Baltzell, VP, Head of HR at: Meesha.Baltzell@sio2med.com