Josephine Wray Email & Phone Number | I am a Quality Assurance professional with over 15 years of experience in GMP Quality Assurance processes, procedures and international regulation. I have worked in laboratories, manufacturing, packaging and shipment areas. I have managed a team of QA Analytical professionals, and manufacturing operators within the pharmaceutical field. CAREER EXPERIENCE • Process Improvements : New Products Introduction and Product Lifecycle • Product experience in: Tablets, Capsules, and Ointments (including Sterile) • Review and Approved Change Control’s • Managed (review and approved, tracked and reported) Non –Conformances: Deviations, Complaints, Quality Investigations and related CAPA’s. • Auditing - Managed internal audit system and assisted in Client and Regulatory audits. • Review and Approval Qualification/Validation Protocols/Reports e.g Process, Cleaning Equipment and Facilities (Temperature Mapping). • Review and Approval Manufacturing and Packaging Batch records • Managed and co-ordinated site Product Recall activites. • Managed QA and GMP training, including creating and implementing a competency training programme. • Managed Quality Documentation System. (including Writing, Reviewing and Approval of SOP’s) • Managed Product Stability Programme • Technical Transfers of Analytical Methods • Preparation of Specifications, Methods, Stability documents for NDA Regulatory submission. (from Raw Material to Finished Product.) • Provided information/documents to support Regulatory Changes e.g Initiated and successfully achieved a change of specification for two products with the appropriate regulatory authorities. (MHRA and FDA) • Written Qualification/Validation Protocols/Reports(Process and Cleaning) Training/Membership: ISO 9001:2015 Lead Auditor Certificate ISO 9001:2015 Internal Auditor Certificate ASQ (American Society for Quality) Full Member RAPS (Regulatory Affairs Professional Society) Associate Member PSG (Pharmaceutical Science Group Member

Josephine Wray

I am a Quality Assurance professional with over 15 years of experience in GMP Quality Assurance proc...
Toronto, Toronto, Canada

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Josephine Wray’s Email josephine.wray@resilience.com

Josephine Wray’s Phone Numbers +1 617-245-****

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Josephine Wray’s Location Toronto, Toronto, Canada

Josephine Wray’s Current Industry Resilience

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Work Experience

Resilience

Quality Compliance Manager

2020-10-01 00:00:00 - Present

Therapure Biopharma

Quality Assurance Manager, Compliance

2020-03-01 00:00:00 - 2020-10-01 00:00:00

Pharmeng Technology

Senior Consultant

2014-09-01 00:00:00 - 2020-03-01 00:00:00

Abbott Nutrition

Project Qa Executive (Qa Project Leader)

2012-07-01 00:00:00 - 2013-08-01 00:00:00

Fisher Clinical Services

Quality Assurance Executive

2010-01-01 00:00:00 - 2012-06-01 00:00:00

Gw Pharmaceuticals

Document Control Officer, Quality Assurance

2003-01-01 00:00:00 - 2004-08-01 00:00:00

Gsk

Team Leader Analytical Sciences

2000-08-01 00:00:00 - 2002-01-01 00:00:00

Pfizer

Research Assistant

1996-08-01 00:00:00 - 1997-05-01 00:00:00

Ciba

Analytical Technician

1995-08-01 00:00:00 - 1996-07-01 00:00:00

Ferguson And Menzies

Laboratory Chemist

1993-11-01 00:00:00 - 1995-07-01 00:00:00

Skills

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Languages

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FAQ About Josephine Wray

Josephine Wray is located at
Toronto, Toronto, Canada

Josephine Wray is a I am a Quality Assurance professional with over 15 years of experience in GMP Quality Assurance processes, procedures and international regulation. I have worked in laboratories, manufacturing, packaging and shipment areas. I have managed a team of QA Analytical professionals, and manufacturing operators within the pharmaceutical field. CAREER EXPERIENCE • Process Improvements : New Products Introduction and Product Lifecycle • Product experience in: Tablets, Capsules, and Ointments (including Sterile) • Review and Approved Change Control’s • Managed (review and approved, tracked and reported) Non –Conformances: Deviations, Complaints, Quality Investigations and related CAPA’s. • Auditing - Managed internal audit system and assisted in Client and Regulatory audits. • Review and Approval Qualification/Validation Protocols/Reports e.g Process, Cleaning Equipment and Facilities (Temperature Mapping). • Review and Approval Manufacturing and Packaging Batch records • Managed and co-ordinated site Product Recall activites. • Managed QA and GMP training, including creating and implementing a competency training programme. • Managed Quality Documentation System. (including Writing, Reviewing and Approval of SOP’s) • Managed Product Stability Programme • Technical Transfers of Analytical Methods • Preparation of Specifications, Methods, Stability documents for NDA Regulatory submission. (from Raw Material to Finished Product.) • Provided information/documents to support Regulatory Changes e.g Initiated and successfully achieved a change of specification for two products with the appropriate regulatory authorities. (MHRA and FDA) • Written Qualification/Validation Protocols/Reports(Process and Cleaning) Training/Membership: ISO 9001:2015 Lead Auditor Certificate ISO 9001:2015 Internal Auditor Certificate ASQ (American Society for Quality) Full Member RAPS (Regulatory Affairs Professional Society) Associate Member PSG (Pharmaceutical Science Group Member

Josephine Wray currently works in the Resilience |

No Languages Available

Josephine Wray has prior
experience in the following industries:
Therapure Biopharma | Pharmeng Technology | Abbott Nutrition | Fisher Clinical Services | Gw Pharmaceuticals | Gsk | Pfizer | Ciba | Ferguson And Menzies

Josephine Wray has the following professional experience:
Resilience | Therapure Biopharma | Pharmeng Technology | Abbott Nutrition | Fisher Clinical Services | Gw Pharmaceuticals | Gsk | Pfizer | Ciba | Ferguson And Menzies