| Distance: | Resume alert | Resumes 211 - 220 of 7109 |
Quality Assurance Management & Nucleaqr Utility Oversite
Aiken, SC, 29801
... by the Nuclear Regulatory Commission (NRC) as a Subject Matter Expert (SME) in the field of Corrective Action Program (CAPA) & Performance Improvement (HPI) Recognized by INPO & IAEA as a Quality Assurance Program Subject Matter Expert Expertise ... - 2025 Dec 18
... by the Nuclear Regulatory Commission (NRC) as a Subject Matter Expert (SME) in the field of Corrective Action Program (CAPA) & Performance Improvement (HPI) Recognized by INPO & IAEA as a Quality Assurance Program Subject Matter Expert Expertise ... - 2025 Dec 18
Operations Leader & Business Analyst, 20+ Years Experience
Santa Clarita, CA
... Manage CAPA investigations and implementations across packaging/labeling, master data management, configuration management, and record retention processes. Partner with global teams to implement technical literature and product lifecycle management ... - 2025 Dec 17
... Manage CAPA investigations and implementations across packaging/labeling, master data management, configuration management, and record retention processes. Partner with global teams to implement technical literature and product lifecycle management ... - 2025 Dec 17
Materials Planning & Supply Chain Leadership (30+ Years)
Santa Clara, CA, 95051
... [cont’d next page] CHRIS BROWN Page 2 • Participated in SCAR/CAPA/NCMR creation, review and resolution. • Followed rigorous QMS / FDA regulations. • Created and maintained manual MRP for majority of production parts, both direct and indirect. ... - 2025 Dec 14
... [cont’d next page] CHRIS BROWN Page 2 • Participated in SCAR/CAPA/NCMR creation, review and resolution. • Followed rigorous QMS / FDA regulations. • Created and maintained manual MRP for majority of production parts, both direct and indirect. ... - 2025 Dec 14
Quality Inspector, QA Technician, Manufacturing, Assembly lines, ASQ
Minneapolis, MN, 55404
... • Initiated NCMR's and worked closely with Quality Engineers, as well as Manufacturing Engineers to resolve the issues and assist in carrying out CAPA's. • Assisted in improving the incoming goods inspection processes by implementing a skip lot ... - 2025 Dec 14
... • Initiated NCMR's and worked closely with Quality Engineers, as well as Manufacturing Engineers to resolve the issues and assist in carrying out CAPA's. • Assisted in improving the incoming goods inspection processes by implementing a skip lot ... - 2025 Dec 14
Biotech QC/QA Lead with Auditing Expertise
Natick, MA
... • Expert with pre-approval of investigation, deviation, Root Cause Analysis (RCA), CAPA, OOS, OOT, and LE. • Over 30 years’ experience of EH&S and usage of PPE. • Lead continuous improvement on targeted business processes, using Lean Sigma, to ... - 2025 Dec 10
... • Expert with pre-approval of investigation, deviation, Root Cause Analysis (RCA), CAPA, OOS, OOT, and LE. • Over 30 years’ experience of EH&S and usage of PPE. • Lead continuous improvement on targeted business processes, using Lean Sigma, to ... - 2025 Dec 10
Quality Manager with 22 Years in OEM/EMS Industry
Coimbatore, Tamil Nadu, India
... Process Excellence: Experienced in process validation (FAI, PFMEA, DOE) for New Product Introductions (NPI), supplier quality programs (IQC, OQC, SPC, RCA/CAPA), and driving Kaizen projects. Problem Solving & Continuous Improvement: Skilled in root ... - 2025 Dec 10
... Process Excellence: Experienced in process validation (FAI, PFMEA, DOE) for New Product Introductions (NPI), supplier quality programs (IQC, OQC, SPC, RCA/CAPA), and driving Kaizen projects. Problem Solving & Continuous Improvement: Skilled in root ... - 2025 Dec 10
Electrical and Quality Assurance Specialist
Rowland Heights, CA
... performing Supplier Audits, Supplier Source Inspection (SSI) including application of quality tools in identifying and resolving CAPA and Supplier Corrective Actions (SCAR) related to Class-III medical devices •Possess more 15 years of experience in ... - 2025 Dec 08
... performing Supplier Audits, Supplier Source Inspection (SSI) including application of quality tools in identifying and resolving CAPA and Supplier Corrective Actions (SCAR) related to Class-III medical devices •Possess more 15 years of experience in ... - 2025 Dec 08
Medical Device Design Quality & Validation Engineer
Irving, TX
... Successfully utilized cross-functional teams to resolve non-conformances (NCRs) through detailed investigations and the implementation of corrective and preventive actions (CAPA). Skilled in statistical analysis and process optimization using Six ... - 2025 Dec 08
... Successfully utilized cross-functional teams to resolve non-conformances (NCRs) through detailed investigations and the implementation of corrective and preventive actions (CAPA). Skilled in statistical analysis and process optimization using Six ... - 2025 Dec 08
Sterile Manufacturing / Biopharma Specialist Resume
Durham, NC, 27701
... Operations & Equipment Setup Electrical & Mechanical Assembly cGMP / GDP Compliance & Process Documentation Root Cause Analysis & CAPA Support Lean / 6S / Kaizen Implementation Autoclaving & Material Preparation Team Training, Coaching & Leadership ... - 2025 Dec 08
... Operations & Equipment Setup Electrical & Mechanical Assembly cGMP / GDP Compliance & Process Documentation Root Cause Analysis & CAPA Support Lean / 6S / Kaizen Implementation Autoclaving & Material Preparation Team Training, Coaching & Leadership ... - 2025 Dec 08
Avocate expérimentée en droit des assurances et gestionnaire senior
Algeria
... FORMATION ET DIPLÔMES Certificat d'Aptitude à la Profession d'Avocat (CAPA) [2007] Licence Juridique et Administrative [2006] Baccalauréat – Série Lettres et Sciences Humaines [Juin 2001] Formations Complémentaires Diplôme en Langue des Signes ... - 2025 Dec 07
... FORMATION ET DIPLÔMES Certificat d'Aptitude à la Profession d'Avocat (CAPA) [2007] Licence Juridique et Administrative [2006] Baccalauréat – Série Lettres et Sciences Humaines [Juin 2001] Formations Complémentaires Diplôme en Langue des Signes ... - 2025 Dec 07