×
Register Here to Apply for Jobs or Post Jobs. X

LOX Product Engineer

Job in Ball Ground, Cherokee County, Georgia, 30107, USA
Listing for: CAIRE Inc.
Full Time position
Listed on 2026-01-01
Job specializations:
  • Engineering
    Manufacturing Engineer, Quality Engineering
  • Manufacturing / Production
    Manufacturing Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 45 - 55 USD Hourly USD 45.00 55.00 HOUR
Job Description & How to Apply Below
Location: Ball Ground

LOX Production Engineer (Manufacturing)

Classification: Contract

Base Pay Range

$45.00/hr - $55.00/hr

Job Description

This key engineering role will be responsible for supporting CAIRE, Inc. Liquid Oxygen medical products (stationary and portable Liquid Oxygen systems) manufacturing by creating and improving and validating manufacturing processes, authoring all associated manufacturing documentation, and maintaining compliance with our quality system.

Essential Functions
  • Responsible for Device Master Record (DMR) deliverables - validation and qualification of new product launches, manufacturing equipment, software and processes leveraging standard qualification approaches (IQ/OQ/PQ).
  • While utilizing lean manufacturing tools, design, sustain and improve manufacturing assembly lines, refining BOMs, workflow processes, PFMEAs and detailed work instructions.
  • Create and manage production changes through Engineering Change Orders (ECO).
  • Maintain compliance with medical device quality system which includes leading and/or supporting corrective action Preventative action initiatives (CAPAs), discrepant material disposition and Engineering Change Order (ECO) implementation.
  • Provide technical support for failure analysis and root cause investigation of product failures.
  • Identify and implement continuous improvement projects with respect to first pass yield, cycle time reduction, product reliability, capacity enhancement and cost reduction, utilizing a DMAIC and DMADV structure.
  • Work with Quality group to ensure that the team follows appropriate Good Manufacturing Processes (GMP), design history file (DHF), and device history record (DHR) guidelines per FDA requirements, and support design reviews in accordance with product development procedures.
  • Improve product quality, yields, and reduce cost.
  • Complete cost analysis and lead cost reduction efforts.
  • Analyze instrument-manufacturing line from a risk perspective (PFMEA) to incorporate and validate critical tests used in manufacturing.
  • Provide production line support for day-to-day engineering issues on core equipment.
  • Provide technical support analyzing and /or performing failure analysis for discrepant production components, assemblies and field returns.
  • Other related duties.
Required

Education and Experience
  • Successful experience leading projects, and juggling multiple business demands.
  • Minimum of five years’ engineering experience manufacturing cryogenic medical products, or complex electro-mechanical products.
  • Experience with mechanical CAD (Solidworks, CREO), MS Project software.
  • Experience in using Minitab for statistical analysis, Gage R&R.
  • Experience with programming languages such as Java, Python and SQL.
  • Experience developing products from concept to volume manufacturing.
  • Mechanical design and analysis expertise desired.
  • DMAIC and Lean Six Sigma experience, black belt preferred.
  • Prior responsibility for validation of processes, equipment and products.
  • Strong quantitative process development skills including (p)
    FMEA, tolerance analysis, DoE, SPC, GR&R, and Cpk/Cp.
  • Excellent organizational skills;
    Able to manage multiple fast-paced projects simultaneously.
  • Ability to communicate effectively and professionally across a range of technical disciplines with a broad slate of stakeholders, including management, peers, customers, and suppliers.
  • Ability to work in a Matrix org structure with cross functional Value Streams.
Preferred

Education and Experience
  • Experience in an ISO 18777, ISO 13485, ISO 9001, or medical device manufacturing environment preferred.
  • Cryogenics (Heat transfer, Thermodynamics) knowledge is a plus.

Additional Eligibility

Qualifications:

Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job.

Duties, responsibilities and activities may change at any time with or without notice.

Supervisory Responsibility: No

Physical Demands: This is largely a physically active role. This would require the ability to lift, bend, or stand as necessary.

Travel: Yes, Travel up to 10% per year.

#J-18808-Ljbffr
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)

Job Posting Language
Employment Category
Education (minimum level)
Filters
Education Level
Experience Level (years)
Posted in last:
Salary