Jonathan Colletti Email & Phone Number | I have a passion for helping stakeholders navigate regulatory requirements to deliver cutting edge therapies to patients. My experience includes equipment and automation commissioning, qualification, and validation (CQV) for cell and gene therapy manufacturing facilities. My philosophy for regulatory compliance utilizes a science and risk-based approach that aligns with current industry best practices and FDA expectations. This approach ensures patient safety and product quality through the efficient use of company resources and input from subject matter experts, while simultaneously reducing audit surface area by focusing on critical system functionality and good engineering practices.

Jonathan Colletti

I have a passion for helping stakeholders navigate regulatory requirements to deliver cutting edge t...
Raleigh-Durham-Chapel Hill Area, Raleigh-Durham-Chapel Hill Area, United States

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Jonathan Colletti’s Email jcolletti@sequenceqcs.com

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Jonathan Colletti’s Location Raleigh-Durham-Chapel Hill Area, Raleigh-Durham-Chapel Hill Area, United States

Jonathan Colletti’s Current Industry Astellas Gene Therapies

Jonathan Colletti’s Prior Industry Sequence | Viwinco Windows | Basf

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Work Experience

Astellas Gene Therapies

Validation Engineer

2023-03-01T00:00:00.000Z - Present

Sequence

Senior Consultant - Project Engineering

2022-08-01T00:00:00.000Z - 2023-03-01T00:00:00.000Z

Viwinco Windows

Product Engineer

2019-01-01T00:00:00.000Z - 2019-10-01T00:00:00.000Z

Basf

Project Engineering Co-op

2018-05-01T00:00:00.000Z - 2018-08-01T00:00:00.000Z

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FAQ About Jonathan Colletti

Jonathan Colletti is located at
Raleigh-Durham-Chapel Hill Area, Raleigh-Durham-Chapel Hill Area, United States

Jonathan Colletti is a I have a passion for helping stakeholders navigate regulatory requirements to deliver cutting edge therapies to patients. My experience includes equipment and automation commissioning, qualification, and validation (CQV) for cell and gene therapy manufacturing facilities. My philosophy for regulatory compliance utilizes a science and risk-based approach that aligns with current industry best practices and FDA expectations. This approach ensures patient safety and product quality through the efficient use of company resources and input from subject matter experts, while simultaneously reducing audit surface area by focusing on critical system functionality and good engineering practices.