Overview
On Site
USD 55.00 - 70.00 per hour
Full Time
Skills
MI
Marketing intelligence
Functional requirements
Testing
Billing
Computer Aided Design (CAD)
Supervision
Attention to detail
Motivation
Management
PPAP
Process engineering
Program management
Mechanical engineering
Vendor management
Specification
Manufacturing
Assembly
FMEA
Risk analysis
Process control
Design
Medical devices
Pharmaceutics
Aerospace
Quick learner
Welding
Design of experiments
OQ
PQ
Layout
Job Details
Location: Kalamazoo, MI
Salary: $55.00 USD Hourly - $70.00 USD Hourly
Description: Our client is currently seeking a Senior Engineer, Engineering for a 12 month + contract.
Description/Comment:
Designs, validates and brings new products to market. Specifies precise new product functional requirements; designs, tests and integrates components to produce final designs; and evaluates the design's overall effectiveness, cost, reliability and safety. Designs, develops, executes and evaluates fitness-for-use testing, product specifications and process validation plans; creates and reviews material part specifications and bills of materials. Collaborates with internal manufacturing partners, contract manufacturers, designers and product specialists to optimize designs for manufacturability. Utilizes CAD (Computer Aided Design) or CAE (Computer Aided Engineering) systems to model new designs and produce detailed engineering drawings. This is an individual contributor role that requires the use of judgement in applying professional expertise and is expected to work independently with minimal supervision. Roles typically require a university degree or an extensive amount of practical knowledge gained through experience. Job requires an understanding and application of procedures and concepts of own discipline. The job requires attention to detail in making evaluative judgements based on the analysis of factual information.
Preferred Medical Device experience.
Self-Motivation and task management is expected Experience with PPAP, process validation, process development Program Management experience is an asset. Project is electro-mechanical with imbedded software - experience in these types of projects is required.
It is an individual contributor with ~5 years' experience.
Supplier/Vendor Management will be a key function of the job. We want some people with those skill sets. The process engineers all work very closely with external vendor procuring the parts and ensuring those parts meet our specifications.
Emphasis Process Validation. We have gotten candidates that had equipment qualification (i.e., ensuring a single piece of equipment is functioning as expected and produces the correct results) but we need people that have experience looking at and entire manufacturing assembly process and validating the whole process. Key word like pFMEA, Risk Analysis, Process Control Plans should help narrow the candidate.
Production Part Approval. We need someone who is capable of taking a part design and working with the vendor, review their process and define the process that will ensure that the vendor delivers the correct part every time.
Ideally, we want the candidates to have medical device experience and may consider someone with experience in regulated industries like pharma, automotive and aerospace.
Want to add that they are a, team player, quick learner, problem solver, self-motivated. We need someone who can be given objectives, then define the task themselves for review, identify problems and propose solutions.
Any experience working with Pressure Leak systems will be a huge asset
Plastics Joining Welding experience will be preferred
Additional Job Details:
One Candidate will be support LPIM project Design of experiments OQ/PQ. Second Candidate will be responsible for development and validating the Process/Software/Applications for the production Equipment.
Top 3 must haves to perform the Job:
Layout Experience; Equipment Validation
Minimum of 2 years; 3 or more preferred experience.
Contact:
This job and many more are available through The Judge Group. Please apply with us today!
Salary: $55.00 USD Hourly - $70.00 USD Hourly
Description: Our client is currently seeking a Senior Engineer, Engineering for a 12 month + contract.
Description/Comment:
Designs, validates and brings new products to market. Specifies precise new product functional requirements; designs, tests and integrates components to produce final designs; and evaluates the design's overall effectiveness, cost, reliability and safety. Designs, develops, executes and evaluates fitness-for-use testing, product specifications and process validation plans; creates and reviews material part specifications and bills of materials. Collaborates with internal manufacturing partners, contract manufacturers, designers and product specialists to optimize designs for manufacturability. Utilizes CAD (Computer Aided Design) or CAE (Computer Aided Engineering) systems to model new designs and produce detailed engineering drawings. This is an individual contributor role that requires the use of judgement in applying professional expertise and is expected to work independently with minimal supervision. Roles typically require a university degree or an extensive amount of practical knowledge gained through experience. Job requires an understanding and application of procedures and concepts of own discipline. The job requires attention to detail in making evaluative judgements based on the analysis of factual information.
Preferred Medical Device experience.
Self-Motivation and task management is expected Experience with PPAP, process validation, process development Program Management experience is an asset. Project is electro-mechanical with imbedded software - experience in these types of projects is required.
It is an individual contributor with ~5 years' experience.
Supplier/Vendor Management will be a key function of the job. We want some people with those skill sets. The process engineers all work very closely with external vendor procuring the parts and ensuring those parts meet our specifications.
Emphasis Process Validation. We have gotten candidates that had equipment qualification (i.e., ensuring a single piece of equipment is functioning as expected and produces the correct results) but we need people that have experience looking at and entire manufacturing assembly process and validating the whole process. Key word like pFMEA, Risk Analysis, Process Control Plans should help narrow the candidate.
Production Part Approval. We need someone who is capable of taking a part design and working with the vendor, review their process and define the process that will ensure that the vendor delivers the correct part every time.
Ideally, we want the candidates to have medical device experience and may consider someone with experience in regulated industries like pharma, automotive and aerospace.
Want to add that they are a, team player, quick learner, problem solver, self-motivated. We need someone who can be given objectives, then define the task themselves for review, identify problems and propose solutions.
Any experience working with Pressure Leak systems will be a huge asset
Plastics Joining Welding experience will be preferred
Additional Job Details:
One Candidate will be support LPIM project Design of experiments OQ/PQ. Second Candidate will be responsible for development and validating the Process/Software/Applications for the production Equipment.
Top 3 must haves to perform the Job:
Layout Experience; Equipment Validation
Minimum of 2 years; 3 or more preferred experience.
Contact:
This job and many more are available through The Judge Group. Please apply with us today!
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.