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Posted 30+ days ago

Posted 30+ days ago

$110,000 - $160,000 / year
Posted 30+ days ago

$19 - $28 / hour
Posted 30+ days ago

$62,000 - $100,000 / year
Posted 5 days ago
$70,000 - $85,000 / year
Posted 1 week ago

$17 - $25 / hour
Posted 30+ days ago
$23 - $34 / hour
Posted 30+ days ago

$21 - $25 / hour
Posted 6 days ago

$23 - $28 / hour
Posted 3 weeks ago

$55,000 - $75,000 / year
Posted 30+ days ago

Posted 1 week ago

$140,000 - $150,000 / year
Posted 3 weeks ago

$20 - $31 / hour
Posted 2 weeks ago

$16+ / hour
Posted 30+ days ago

Posted 30+ days ago

$15 - $20 / hour
Posted 30+ days ago

$16 - $18 / hour
Posted 1 week ago

Posted 30+ days ago
$16 - $17 / hour
Posted 30+ days ago
Quality Engineer (Manufacturing)
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Job Description
Mack Molding is recognized as one of the world's premier custom manufacturers of high quality complex parts, assemblies, and total products in plastic and metal. We have been in business since 1920, and have grown to over 2000 employees in seven plants located throughout the eastern United States.
Mack Molding offers a variety of services throughout its numerous facilities, resulting in many diverse career paths and advancement opportunities. And when new opportunities arise, whether on the manufacturing floor, out in the field, or in the corporate offices, Mack strives to promote its talent from within.
- This role involves working in an ITAR-controlled environment. The successful candidate will have a strong technical background, problem-solving skills, and the ability to work within the strict compliance requirements of ITAR regulations.
Essential Responsibilities:
Support new business development
Provides support to new business development relating to quality matters as needed
Draft preliminary Quality Plan, if appropriate
Provides cost and time estimates for anticipated quality department services such as metrology or validation services
Functions as a resource for applicable ISO Program and QSR Program requirements
Support Program Launch and Product Realization as functional department representative assigned to team and Program Manager
Reviews new program drawings/information/customer specifications to understand program requirements
Determines quality and reliability standards and ensures dimensional and cosmetic requirements, as well as customer specifications, are defined and understood.
Drafts program Quality Plan (as required) and metrology labor plan to include definition of required fixtures, calibration and metrology requirements and measurement methods needed to meet customer requirements for approval
Drafts other required quality documentation such as Dimensional Visual Quality Requirements (DVQR's) and new product inspection techniques
Confirms customer agreement on GD&T callouts/interpretations and all critical dimensions of program when required
Prepares Failure Mode Effects Analysis (FMEA), as needed
Prepares Traveler Document
Develops required Control/Test methods
Ensures First Article Inspection (FAI) and Capability Studies are scheduled and completed
Completes FAI and capability study analysis for submission to customer
Authors operational qualification (OQ) and performance qualification (PQ) protocols and provides training for protocol participants
Oversees the execution of assigned OQ and PQ studies to ensure compliance with protocol requirements and completion of study tasks
Authors OQ and PQ Completion Reports to include resolution of any deviations recorded and overall study conclusion
Establishes "golden sample" standards and prepares and submits to customer via customer approval form (CAF) as required
Attends program team meetings to address quality-related matters
Performs assigned activities in a timely manner
Provide continuous quality engineering support through program end of life.
Completes Certificates of Conformance (CoC) for outgoing products, where required
Collects and analyzes production line data to monitor yield and defect performance
Ensures golden samples are retained and controlled
Maintains Device History Records (DHR) as necessary
Performs periodic risk assessments, as required
Assists Purchasing Department with maintaining vendor quality requirements
Continuously monitors production to identify quality-related customer issues and supports corrective action plans when necessary
Issue or authorize CCR's as needed. Manages the return of goods, assignments and close out of RC/CA.
Conducts root cause investigation and develops corrective action plans for assigned problem reports (PSRs) and quality issues
Manages product and process change control and notification to ensure required Engineering Change Orders (ECOs) are generated and approved by the customer prior to implementation.
Attends program team meetings as necessary to resolve program quality issues to maintain customer satisfaction
Support QBR's with customer and provides/presents quality-related topics
Participates in customer, certified body, and regulatory audits as a subject matter expert for assigned products and processes
Working knowledge of Statistical techniques & sampling plans and of Quality Systems Regulations. Bachelors degree (B.A.) in technical field desired, plus 2 years related experience preferred. Experience in medical device-manufacturing environment, and experience with Six Sigma or Lean are preferred.
This position requires access to information subject to the International Traffic in Arms Regulations and/or the Export Administration Regulations. As such, this position is open only to applicants who qualify as "U.S. Persons" as defined by 22 C.F.R. §120.15 is required. "U.S. Person" includes U.S. Citizen, lawful permanent resident, refugee, or asylee."
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