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Stephen Bush Email & Phone Number

Inspiring Others to Unlock their Full Potential is My Favorite Job at Thermo Fisher Scientific
Location: Greater Orlando, United States 13 work roles 1 school
1 work email found @thermofisher.com 1 phone found area 856 LinkedIn matched
✓ Verified Jul 2026 4 data sources Profile completeness 100%

Contact Signals · 1 work email · 1 phone

Work email s****@thermofisher.com
Direct phone (856) ***-****
LinkedIn Profile matched
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Current company
Role
Inspiring Others to Unlock their Full Potential is My Favorite Job
Location
Greater Orlando, United States

Who is Stephen Bush? Overview

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Quick answer

Stephen Bush is listed as Inspiring Others to Unlock their Full Potential is My Favorite Job at Thermo Fisher Scientific, based in Greater Orlando, United States. AeroLeads shows a work email signal at thermofisher.com, phone signal with area code 856, and a matched LinkedIn profile for Stephen Bush.

Stephen Bush previously worked as Supplier Quality Manager at Thermo Fisher Scientific and Staff Supplier Quality Engineer at Thermo Fisher Scientific. Stephen Bush holds Associate'S Degree, Associate Of Arts With A Concentration In Foundations Of Business from University Of Phoenix.

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Email format at Thermo Fisher Scientific

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{first}.{last}@thermofisher.com
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AeroLeads found 1 current-domain work email signal for Stephen Bush. Compare company email patterns before reaching out.

Profile bio

About Stephen Bush

Experienced QA professional who specializes in problem solving and developing and improving business processes/Quality Systems. A leader who can manage projects, work within a cross-functional team or perform independently. Focus areas include all aspects of complaint handling, internal/supplier audits, Quality System improvements, and SOP development and implementation. Additional skills and experience include:- Adverse Event (AE) reporting: FDA MDR (MedWatch), EU Vigilance, etc.- Project manager/lead for QS improvements, CAPA, computer software validation (CSV), etc.- CAPA- Nonconformance (NC) handling- Training- Document management/control- Change management/control- SharePoint, AssurX CATSWeb, TrackWise, MS Office, MS Project- Compliance with ISO 13485 and 21 CFR Part 820

Listed skills include Capa, Fda, Quality System, Iso 13485, and 37 others.

Current workplace

Stephen Bush's current company

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Thermo Fisher Scientific
Thermo Fisher Scientific
Inspiring Others to Unlock their Full Potential is My Favorite Job
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13 roles

Stephen Bush work experience

A career timeline built from the work history available for this profile.

Consultant: Qa Manager/Project Manager

Rgp

Irvine, Ca, Us

Provide QA consulting and project management services for Fortune 500 medical device/pharma/supply chain clients in the Southern NJ/Philadelphia region. My role as a quality-focused project manager was based in supply chain and logistics for projects in the US and Europe.

May 2017 - Apr 2019

Capa/Complaint Analyst Iii

Raritan, New Jersey, Us

(contract employee via Kelly Project Services)- Oversee CAPA/Deviation process, including planning, metrics and reporting to management.- Triage a variety of US and OUS pharmaceutical product quality complaints for investigation and classification purposes and assignment further downstream. - Liaise with call centers and other customer facing representatives on a daily basis.- Conduct outreach activities with consumers, pharmacies and health care providers to gather additional complaint and product information- Use TrackWise for record-keeping and to manage complaint triage workflow.

Oct 2016 - May 2017

Quality Systems Manager

Aries Filterworks

- Management Representative for the ISO 9001 QMS.- Champion CAPA’s, continuous improvements and cost reduction efforts.- Lead complaint and NC investigations.- Liaise with suppliers to resolve quality issues/SCAR’s.- Respond to customer inquiries.- Manage projects and develop and implement new processes.- Manage changes, document control and calibration program.- Support equipment and PM program.- Coordinate validation program.- Support supplier selection and monitoring program.- Support new product development and other D&D activities.- Gather, analyze and report on quality data/trends.- Train personnel at all levels of the organization on the QMS and associated processes.- Experience with NSF and WQA certification.

Feb 2015 - Oct 2016

Sr. Quality Specialist

Plano, Tx, Us

- Corporate administrator for the global complaint system. - Develop, improve and expand the use of the electronic QMS processes.- Validate electronic QMS processes.- Author software validation protocols, test scripts, validation summary reports, etc.- Investigate and resolve deviations, NC's and other issues (software and QMS-related).- Provide training for the global complaint system and other aspects of the software.- Lead internal audits.Note: Argon Medical Devices acquired Angiotech’s interventional product lines on April 12, 2013.

Apr 2013 - Feb 2015

Quality Compliance Coordinator

Westwood, Massachusetts, Us

- Lead/Participate in QS improvement initiatives, corporate and facility projects, etc.- Develop tracking systems and metrics to monitor product/process performance- Train and mentor/coach personnel in performing various QS functions- Lead internal audits and supplier audits- Coordinate and lead software validation activities- Coordinate the corporate document/change control process (SharePoint)- Develop and document policies, procedures and work instructions to comply with applicable standards/regulations- Review and approve corporate QS documents- Administer the global complaint system (AssurX CATSWeb)

Jul 2012 - Apr 2013

Qa Consultant

Westwood, Massachusetts, Us

- Lead/Participate in QS improvement initiatives, corporate and facility projects, etc.- Develop tracking systems and metrics to monitor product/process performance- Train and mentor/coach personnel in performing various QS functions- Lead internal audits and supplier audits- Coordinate and lead software validation activities- Develop and document policies, procedures and work instructions to comply with applicable standards/regulations

May 2009 - Jul 2012

Quality Systems Coordinator

Westwood, Massachusetts, Us

- Evaluate, trend, and report field complaints to management- Document and submit adverse event reports to regulatory authorities (FDA MedWatch/MDR’s and EU Vigilance)- Lead internal audits and supplier audits- Lead CAPA projects/initiatives and participate in QS improvement initiatives- Develop tracking systems and metrics to monitor product/process performance- Develop and document policies, procedures and work instructions to comply with applicable standards/regulations- Train and mentor/coach personnel in performing QS functions- Coordinate and lead various projects and improvement activities, including software validation efforts

Mar 2008 - May 2009

Project Leader / Sr. Product Performance Specialist

Wayne, Pa, Us

- Evaluate, trend, and report field complaints to management- Coordinate complaint-related activities with satellite facilities- Input with CAPA projects/initiatives and participate in QS improvement initiatives- Develop and document policies, procedures and work instructions to comply with applicable standards/regulations- Train and mentor/coach personnel in performing complaint investigations- Coordinate and lead various projects and improvement activities, including software validation efforts

Mar 2007 - Mar 2008

Quality System Associate

Us

- Coordinate and perform facility and corporate internal audits- Develop and document procedures and work instructions to comply with applicable standards/regulations- Maintain the corporate QS and Environmental Management System (EMS)- Train and mentor/coach personnel involved with QS and EMS activities- Coordinate QS and EMS activities with satellite manufacturing facilities- Input with CAPA projects/initiatives and participate in QS and EMS improvement initiatives

Jan 2006 - Mar 2007

Sr. Quality System Technician

Us

- Coordinate the local internal audit program- Evaluate, trend, and report field complaints to management- Input with CAPA projects/initiatives and root cause analysis- Implement and verify corrective/preventive actions- Perform facility and corporate level internal audits- Maintain the facility QS- Develop and document procedures and work instructions to comply with applicable standards/regulations- Oversee the incoming QA and calibration areas

Nov 2003 - Jan 2006
1 education record

Stephen Bush education

  • University Of Phoenix
    University Of Phoenix
    Associate Of Arts With A Concentration In Foundations Of Business
FAQ

Frequently asked questions about Stephen Bush

Quick answers generated from the profile data available on this page.

What company does Stephen Bush work for?

Stephen Bush works for Thermo Fisher Scientific.

What is Stephen Bush's role at Thermo Fisher Scientific?

Stephen Bush is listed as Inspiring Others to Unlock their Full Potential is My Favorite Job at Thermo Fisher Scientific.

What is Stephen Bush's email address?

AeroLeads has found 1 work email signal at @thermofisher.com for Stephen Bush at Thermo Fisher Scientific.

What is Stephen Bush's phone number?

AeroLeads has found 1 phone signal(s) with area code 856 for Stephen Bush at Thermo Fisher Scientific.

Where is Stephen Bush based?

Stephen Bush is based in Greater Orlando, United States while working with Thermo Fisher Scientific.

What companies has Stephen Bush worked for?

Stephen Bush has worked for Thermo Fisher Scientific, Rgp, The Janssen Pharmaceutical Companies Of Johnson & Johnson, Aries Filterworks, and Argon Medical.

How can I contact Stephen Bush?

You can use AeroLeads to view verified contact signals for Stephen Bush at Thermo Fisher Scientific, including work email, phone, and LinkedIn data when available.

What schools did Stephen Bush attend?

Stephen Bush holds Associate'S Degree, Associate Of Arts With A Concentration In Foundations Of Business from University Of Phoenix.

What skills is Stephen Bush known for?

Stephen Bush is listed with skills including Capa, Fda, Quality System, Iso 13485, Quality Assurance, Medical Devices, 21 Cfr, and Root Cause Analysis.

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