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Mack Molding

Design through FDA-approved plastics manufacturing

Quality Engineer

Quality EngineeringConfirmed live in the last 24 hours
Full-timeArlington, VT, USANo salary listed

About the Job

Requirements

  • High school diploma with five years of related experience, an associate's degree or equivalent from a two-year college or technical school with three years of related experience, or a bachelor's degree in a technical (STEM or Engineering) field with zero to one year of related experience.
  • Working knowledge of statistical techniques and sampling plans, Quality Systems Regulations, and ISO Standards.

Responsibilities

  • Provide quality support for new business development, including drafting preliminary quality plans when appropriate, estimating costs and timing for quality services such as metrology or validation, and serving as a resource for applicable ISO Program and QSR Program requirements.
  • Represent the quality function on program launch and product realization teams; review program drawings, customer specifications, and other information to understand requirements.
  • Determine quality and reliability standards and ensure dimensional, cosmetic, and customer specification requirements are defined and understood.
  • Draft program quality plans and metrology labor plans, including required fixtures, calibration and metrology requirements, and measurement methods.
  • Prepare quality documentation, including Dimensional Visual Quality Requirements and new product inspection techniques.
  • Confirm customer agreement on GD&T callouts, interpretations, and critical program dimensions when required.
  • Prepare Failure Mode and Effects Analyses and traveler documents as needed, and develop required control and test methods.
  • Ensure First Article Inspections and capability studies are scheduled and completed; analyze results for submission to customers.
  • Author operational qualification and performance qualification protocols, train protocol participants, oversee assigned studies for protocol compliance and task completion, and author completion reports documenting deviations and conclusions.
  • Establish golden sample standards and prepare and submit samples to customers for approval when required.
  • Attend program team meetings to address quality matters and perform assigned activities in a timely manner.
  • Provide continuous quality engineering support through the end of each program, including preparing Certificates of Conformance for outgoing products when required, analyzing production-line data for yield and defects, controlling retained golden samples, and maintaining Device History Records as necessary.
  • Perform periodic risk assessments as required and assist Purchasing with vendor quality requirements.
  • Monitor production for customer quality issues and support corrective action plans; issue or authorize CCRs as needed; manage returns, assignments, and closeout of RC/CA.
  • Investigate root causes and develop corrective action plans for assigned problem reports and quality issues.
  • Manage product and process change control and customer notifications, ensuring required Engineering Change Orders are generated and approved by the customer before implementation.
  • Attend program team meetings as needed to resolve quality issues and maintain customer satisfaction; support customer QBRs by providing or presenting quality topics.
  • Participate as a subject matter expert in customer, certified-body, and regulatory audits for assigned products and processes.
  • Perform occasional domestic travel.
  • Perform other duties as assigned.

Desired Qualifications

  • Experience in a 21 CFR Part 820 or ISO 13485 quality-system environment is strongly preferred.
  • Experience with Six Sigma or Lean manufacturing techniques is preferred.

About the Company

Mack Molding

Design through FDA-approved plastics manufacturing

Mack Molding provides end-to-end plastics-based product development and manufacturing across medical and non-medical markets. It offers design, prototyping, engineering, injection molding, sheet metal fabrication, machining, and full product assembly in ISO-certified facilities. MackMedical makes fully assembled Class III PMA devices, surgical instruments, delivery systems, and orthopedic disposables. Its Inman, SC and Statesville, NC divisions focus on large-part molding with about 40 presses, and its goal is to offer a single-source, regulated manufacturing solution to help customers bring products to market quickly.

Company size
201-500
Company stage
Not listed
Total funding
Not listed
Headquarters
Milford, CT
Founded
1920

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