Robert Fishburn

Robert Fishburn

Summary: • Results-driven Manufacturing & Product Engineering Professional with a strong background in process development and validation, technology, product transfers, ... | Huntington Beach, California, United States

Robert Fishburn Email Addresses

fi****@cs****.com Work Email
fi****@cs****.com Personal Email
fi****@cs****.com Personal Email
ro****@no****.com Personal Email
ro****@ev****.com Personal Email

Robert Fishburn Phone Numbers

No phone number available

Robert Fishburn Work History
Evans Manufacturing
Manufacturing Engineering Manager
1 August 2014 — Present
Nobel Biocare
Manufacturing Engineering Manager
1 March 1998 — 1 August 2014
Applied Medical
Product Development Engineer
1 June 1996 — 1 March 1998
Robert Fishburn Current Work Details
Robert Fishburn's Location
Huntington Beach, California, United States
Robert Fishburn's Expertise
  • Summary: • Results-driven Manufacturing & Product Engineering Professional with a strong background in process development and validation, technology, product transfers, fixture design, development, and validation within highly regulated medical device environments including optical, opto-mechanical, and electro-mechanical systems and devices. • 10+ Years’ Experience in writing validation/verification protocols and reports, as well as, documenting and developing manufacturing processes and equipment. Experienced in supporting medical device manufacturing, engineering, and global manufacturing teams, designing and overseeing acquisition of new equipment for automation in production, and setting budgets for production development for new products and process improvements. • Direct experience in the design and development of new Optical medical device products from design, validation to production release; performing design improvements to existing products including review of protocols and test reports before implementations, defining additional testing to add CE (ISO 9000) mark to products and design input on design reviews. • Strong knowledge and experience with ISO 13485 and transfer of Medical Devices from R&D to Manufacturing. Hands on process development in Fixture design, development, assembly, and Fixture IQ, OQ, PQ, and PV • Experienced in Manufacturing procedure development, manufacturing test procedures, engineering changes (ECN), process optimization, as well as, supporting ISO 13485 compliance and transfer of Medical Devices from R&D to Manufacturing. • Experience implementing and managing Lean manufacturing principles, as well as, utilizing strong knowledge of ISO, GMP, GD&T, DFMEA, PFMEA and MDD requirements, and applying a strong background with fit and function evaluation, tolerance studies and design studies using Geometric dimensioning and tolerancing (GD&T)
  • Manufacturing Engineering Manager at Evans Manufacturing, Inc
Robert Fishburn's Current Industry
Evans Manufacturing
Robert Fishburn's Prior Industry
Applied Medical | Nobel Biocare | Evans Manufacturing

Robert Fishburn Education

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Camden County College
Camden County College Associate's degree, Business Administration and Management, General

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FAQ About Robert Fishburn

  • Robert Fishburn is located at Huntington Beach, California, United States

  • Robert Fishburn is a Summary: • Results-driven Manufacturing & Product Engineering Professional with a strong background in process development and validation, technology, product transfers, fixture design, development, and validation within highly regulated medical device environments including optical, opto-mechanical, and electro-mechanical systems and devices. • 10+ Years’ Experience in writing validation/verification protocols and reports, as well as, documenting and developing manufacturing processes and equipment. Experienced in supporting medical device manufacturing, engineering, and global manufacturing teams, designing and overseeing acquisition of new equipment for automation in production, and setting budgets for production development for new products and process improvements. • Direct experience in the design and development of new Optical medical device products from design, validation to production release; performing design improvements to existing products including review of protocols and test reports before implementations, defining additional testing to add CE (ISO 9000) mark to products and design input on design reviews. • Strong knowledge and experience with ISO 13485 and transfer of Medical Devices from R&D to Manufacturing. Hands on process development in Fixture design, development, assembly, and Fixture IQ, OQ, PQ, and PV • Experienced in Manufacturing procedure development, manufacturing test procedures, engineering changes (ECN), process optimization, as well as, supporting ISO 13485 compliance and transfer of Medical Devices from R&D to Manufacturing. • Experience implementing and managing Lean manufacturing principles, as well as, utilizing strong knowledge of ISO, GMP, GD&T, DFMEA, PFMEA and MDD requirements, and applying a strong background with fit and function evaluation, tolerance studies and design studies using Geometric dimensioning and tolerancing (GD&T) Evans Manufacturing

  • Robert Fishburn currently works in the Evans Manufacturing

  • Robert Fishburn specializes in Summary: • Results-driven Manufacturing & Product Engineering Professional with a strong background in process development and validation, technology, product transfers, fixture design, development, and validation within highly regulated medical device environments including optical, opto-mechanical, and electro-mechanical systems and devices. • 10+ Years’ Experience in writing validation/verification protocols and reports, as well as, documenting and developing manufacturing processes and equipment. Experienced in supporting medical device manufacturing, engineering, and global manufacturing teams, designing and overseeing acquisition of new equipment for automation in production, and setting budgets for production development for new products and process improvements. • Direct experience in the design and development of new Optical medical device products from design, validation to production release; performing design improvements to existing products including review of protocols and test reports before implementations, defining additional testing to add CE (ISO 9000) mark to products and design input on design reviews. • Strong knowledge and experience with ISO 13485 and transfer of Medical Devices from R&D to Manufacturing. Hands on process development in Fixture design, development, assembly, and Fixture IQ, OQ, PQ, and PV • Experienced in Manufacturing procedure development, manufacturing test procedures, engineering changes (ECN), process optimization, as well as, supporting ISO 13485 compliance and transfer of Medical Devices from R&D to Manufacturing. • Experience implementing and managing Lean manufacturing principles, as well as, utilizing strong knowledge of ISO, GMP, GD&T, DFMEA, PFMEA and MDD requirements, and applying a strong background with fit and function evaluation, tolerance studies and design studies using Geometric dimensioning and tolerancing (GD&T)

  • Robert Fishburn speaks the following languages: No languages available.

  • Robert Fishburn has prior experience in the following industries: Nobel Biocare , Applied Medical

  • Robert Fishburn has the following professional experience: Evans Manufacturing , Nobel Biocare , Applied Medical .

  • You can view Robert Fishburn’s LinkedIn profile at LinkedIn URL.

  • Robert Fishburn’s work email addresses are [email protected] .

  • Robert Fishburn works at Evans Manufacturing