Supplier Quality Engineer @ Abbott | Jobright.ai
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Supplier Quality Engineer jobs in Westford, MA
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Abbott · 1 week ago

Supplier Quality Engineer

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BiotechnologyEmergency Medicine
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Responsibilities

Assess potential new suppliers for technical, quality, and manufacturing capabilities.
Provide technical support for the introduction of components from a new supplier.
Generate and maintain incoming inspection procedures. Train inspectors to these procedures.
Develop and/or source inspection tools and equipment.
Assist in generating component specifications.
Generate test protocols, monitor testing, issue qualification test reports, and approve components for use in products.
Provide input to Design Engineering on new component technology and assist in component selection with quality and reliability analysis.
Analyze incoming material defects.
Communicate issues to suppliers.
Review new design specifications and provide input from component quality and manufacturability perspective.
Investigate field failures related to supplier materials.
Develop corrective action plan where necessary. Disposition and drive corrective action as necessary.
May supervise inspectors.
Cultivate a wide range of internal networks and begin to develop an extensive external network of resources to facilitate completion of tasks.
Lead a project team of moderate scope.
Provide guidance to less experienced staff. Act as a mentor to lower-level individual contributors.
Influence exerted at peer level and occasionally at first levels of management.
Plan, organize, and prioritize own daily work routine to meet established schedule.
Exercise authority and judgment within defined limits to determine appropriate action.
Failure to achieve results or erroneous decisions or recommendations may cause delays in program schedules and may result in the allocation of additional resources.

Qualification

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Business UnderstandingQuality SystemRegulatory ComplianceTechnical AlternativesProblem-SolvingJudgmentCommunicationMedical device industrySupplier managementProcess validationManufacturingASQ CQE certificationProblem solvingDriving improvements

Required

Bachelors Degree in related field or an equivalent combination of education and work experience.
Minimum 2 years of related work experience with a good understanding of specified functional area.
Working technical knowledge and application of concepts, practices and procedures.
General understanding of business unit/group function.
Will perform this job in a quality system environment.
Failure to adequately perform tasks can result in noncompliance with governmental regulations.
Works on problems of moderate scope where analysis of situations or data requires a review of identifiable factors.
Exercises judgment within defined procedures and practices to determine appropriate action.
Has a broad knowledge of technical alternatives and an understanding of their impact on the systems environment.

Preferred

Experience in Medical Device industry managing suppliers
Experience with Process Validation and manufacturing
ASQ CQE certification preferred
Experience with driving improvements through CAPA

Benefits

Training and career development
Financial security through competitive compensation, incentives, and retirement plans
Health care and well-being programs including medical, dental, vision, wellness, and occupational health programs
Paid time off
401(k) retirement savings with a generous company match

Company

Abbott is engaged in pharmaceuticals and manufacturing healthcare products.

Funding

Current Stage
Public Company
Total Funding
$6.79M
2014-07-14Acquired· by Mylan ($5.3B)
2011-03-15Post Ipo Debt· $0.1M
2009-03-16Post Ipo Debt· $6.69M

Leadership Team

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Miles White
Chief Executive Officer
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Robert Ford
President & Chief Executive Officer
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Company data provided by crunchbase
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