Jason Flores, CQE, CSSGBJason Flores, CQE, CSSGB
Post# of 22465
(Total Views: 410)
Posted On: 04/29/2024 9:36:31 PM
Jason Flores, CQE, CSSGBJason Flores, CQE, CSSGB • 1st • 1st Quality Manager at West Pharmaceutical ServicesQuality Manager at West Pharmaceutical Services
1mo •
1 month ago
I’m happy to share that I’m starting a new position as Quality Assurance Manager at West Pharmaceutical Services!
Former
Quality Assurance ManagerQuality Assurance Manager
Quantum Materials Corp · Full-timeQuantum Materials Corp · Full-time Aug 2022 - Apr 2024 · 1 yr 9 mosAug 2022 - Apr 2024 · 1 yr 9 mos San Marcos, Texas, United StatesSan Marcos, Texas, United States
Start-Up cGMP medical device facility for research and development of diagnostic devices utilizing nanomaterials. Responsible for development, implementation, and oversight of QMS. Accountable for incoming, manufacturing, and compliance quality. Review and approval of regulatory submissions, change control, deviations, CAPAs, commissioning/qualification/validation (CQV), standard operating procedures (SOPs), batch record production, protocols, etc. Regulatory inspections, customer and internal audits. Hire, train, motive, and inspire quality personnel. Develop, initiate, and maintain training program. Provide real time data analytics to support continuous improvement. Monitor critical KPIs and metrics to ensure compliance within QMS.
1mo •
1 month ago
I’m happy to share that I’m starting a new position as Quality Assurance Manager at West Pharmaceutical Services!
Former
Quality Assurance ManagerQuality Assurance Manager
Quantum Materials Corp · Full-timeQuantum Materials Corp · Full-time Aug 2022 - Apr 2024 · 1 yr 9 mosAug 2022 - Apr 2024 · 1 yr 9 mos San Marcos, Texas, United StatesSan Marcos, Texas, United States
Start-Up cGMP medical device facility for research and development of diagnostic devices utilizing nanomaterials. Responsible for development, implementation, and oversight of QMS. Accountable for incoming, manufacturing, and compliance quality. Review and approval of regulatory submissions, change control, deviations, CAPAs, commissioning/qualification/validation (CQV), standard operating procedures (SOPs), batch record production, protocols, etc. Regulatory inspections, customer and internal audits. Hire, train, motive, and inspire quality personnel. Develop, initiate, and maintain training program. Provide real time data analytics to support continuous improvement. Monitor critical KPIs and metrics to ensure compliance within QMS.
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