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60 Kellton Jobs Hiring Near You

Kellton Tech

Manufacturing Engineer

Madison, WI · On-site

$73K - $94K/yr

Job Title: Manufacturing Engineer Location: Onsite - Madison, WI Pay Rate: 48-54/hr. (W2) Job Summary The Manufacturing Engineer is responsible for providing technical guidance and support for ...

Kellton Tech

Inventory Control Specialist II

Houston, TX · On-site

$23/hr

Job Title: Inventory Control Specialist II (3PL Coordinator) Location: Houston, TX Pay Rate: $23/hr (W2) Job Summary: The Inventory Control Specialist II will serve as a key coordinator between the ...

Kellton Tech

Lab Assistant

Salisbury, MD · On-site

$17 - $28/hr

Lab Assistant (Seasonal) Location: Salisbury, MD Pay Rate: $17-28/hr on W2 Duration: Seasonal (6 Months: June-November 2026) Schedule: Monday-Thursday, 5:30 AM - Until Finished (Typically 4:00 PM-4 ...

Kellton Tech

Warehouse Operator III - Bend, OR

Bend, OR · On-site

$25/hr

Title: Warehouse Operator III Location: Bend, OR Duration: 8 months contract with possible extension/fulltime conversion Pay rate: $25/hr M-F 8am-5pm 5x onsite Job Tasks: Read, understand and ...

Kellton Tech

Manufacturing Associate

Walkersville, MD · On-site

$23 - $28/hr

Job Title: Manufacturing Associate (API - Therapeutic Proteins) Location: Walkersville, MD Pay Range: 3rd Shift - $23-28.82/hr. on W2 Pay Range: 2nd Shift - $23-27.57/hr. on W2 Shift Schedule: * 3rd ...

Kellton Tech

Medical Device Assembler

Madison, WI · On-site

$23 - $24/hr

Job Title: Medical Device Assembler Location: Madison, WI (Onsite) Pay Rate: $23-24/hr on W2 Summary Assemble and test medical device assemblies, final products, and accessories per the manufacturing ...

Kellton Tech

QC Analyst II

Vacaville, CA · On-site

$28/hr

Position: QC Analyst II Location: Vacaville, CA (Onsite) Pay Rate : $28/hr. on W2 Summary Under limited supervision, the QC Analyst II is responsible for performing direct materials testing in ...

Kellton Tech

Manufacturing Associate

Portsmouth, NH · On-site

$23/hr

Title: Manufacturing Associate Location: Portsmouth, NH Duration: 12 months contract with possible extension Pay rate: $23/hr (Day Shift) The Manufacturing Associate Level I is responsible for the ...

Kellton Tech

Administrative Assistant I

Boston, MA · On-site

$19.50 - $26.25/hr

Job Title : Administrative Assistant I Job Location : Boston, MA Position is Hybrid : Candidates must have expense report as well as travel arrangement experience. Responsibilities: * Strong ...

Kellton Tech

Warehousing Clerk-Junior

Bolingbrook, IL · On-site

$17/hr

Position: Warehousing Clerk-Junior Location: Bolingbrook, IL Pay Rate: $17/hr. On W2(No Benefits) Contract: 6 Months This is a part time non-exempt temp position. This role is responsible for the ...

Kellton Tech

Material Planner III

Vacaville, CA · On-site

$30 - $32/hr

Job Title: Material Planner III Location: Vacaville, CA Pay Rate: $32/hr on W2 Summary The Material Planner III is responsible for ensuring timely availability of materials to support the product ...

Kellton Tech

Jr. Procurement Associate

Houston, TX · On-site

Position: Jr. Procurement Associate Location: Houston, TX Pay Rate: $23/hr On W2(No Benefits) Contract: 12 Months Job Details Procures materials or other goods and/or coordinates activities involved ...

Kellton Tech

Technical Writer I

Houston, TX · On-site

$23 - $28/hr

Job Title: Technical Writer I Location: Houston, TX (Onsite - 5x/week) Schedule: Monday - Friday | 1st Shift Pay Rate: $23.00 - $28.00/hour (W2) Position Overview: The Technical Writer I is ...

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All JobsKellton Jobs

Manufacturing Engineer

Kellton Tech

Madison, WI • On-site

$73K - $94K/yr

Contractor

Re-posted 2 days ago

Job description

Job Title: Manufacturing Engineer
Location: Onsite – Madison, WI
Pay Rate: 48-54/hr. (W2)

Job Summary

The Manufacturing Engineer is responsible for providing technical guidance and support for manufacturing methods, tooling, test systems, process documentation, and equipment to ensure efficient and compliant medical device manufacturing. This role promotes continuous improvement and ensures all operations conform to internal quality systems, ISO 13485, and regulatory standards. This position involves cross-functional collaboration and direct support to production, engineering, quality, and materials teams. The ideal candidate is an experienced problem-solver with strong technical skills, project management experience, and the ability to work independently in a fast-paced, regulated environment.

Key Responsibilities

  • Own and support manufacturing processes, test systems, tooling, and documentation to ensure compliance with quality and regulatory requirements.
  • Provide process expertise and act as SME for production and process controls.
  • Train and guide production associates on new and existing processes, equipment, and documentation.
  • Troubleshoot production issues and collaborate across teams to implement cost-effective solutions.
  • Develop and revise SOPs, Work Instructions, Process Flow Diagrams, Device History Records, and validation documentation.
  • Participate in continuous improvement efforts to enhance yield, manufacturability, and efficiency.
  • Serve on the Material Review Board (MRB); investigate nonconforming devices and components.
  • Define and execute verification and validation (V&V) plans.
  • Provide inputs on manufacturing strategies, capital planning, and facility maintenance.
  • Assist with cost estimation for new products.
  • Support equipment troubleshooting and participate in supplier development initiatives.
  • Use statistical analysis and lean tools for root cause investigations and process optimization.
  • Perform other duties as needed to support operational and business objectives.

Required Qualifications

  • Education:
  • Associate’s degree in Electrical or Mechanical Engineering (equivalent combination of experience, education, and training accepted).
  • Experience:
  • Experience as a Manufacturing Engineer or Engineering Technician preferred.
  • Prior experience in a medical device manufacturing or technical support role is highly desirable.
  • Technical Skills:
  • Working knowledge of ISO 13485, FDA 21 CFR regulations.
  • Proficient in MS Office (Word, Excel, etc.); SAP and LabView experience a plus.
  • Familiarity with Lean Six Sigma (Green Belt certification preferred).

Key Competencies

  • Leadership and ability to train/guide manufacturing teams.
  • Strong organizational and time management skills.
  • Effective communicator with strong interpersonal and cross-functional collaboration skills.
  • Skilled in root cause analysis, process improvements, and project execution.
  • Ability to manage multiple projects and priorities in a regulated environment.

Organizational Relationship & Scope

  • Reports to the Manufacturing Engineering/Facilities Manager.
  • Works cross-functionally with Sustaining Engineering, Global Device Engineering, QA, Regulatory, and Technical Operations.
  • Responsible for new product introduction, process optimization, and production support.

Working Conditions

  • Mix of hands-on manufacturing line support, computer-based work, and cross-functional meetings.
  • May require extended hours, weekends, or holidays with manager approval.