Company:
Cook Group
Location: Bloomington
Closing Date: 02/11/2024
Hours: Full Time
Type: Permanent
Job Requirements / Description
Overview
This is a Sr. level position requiring 5+ years of subject matter expert CONTROLS experience in Large and Small production equipment (ex: Allen Bradley). The goal of this position is to drive process improvement and increase manufacturing efficiency.
Responsibilities
- Define, identify, procure, and qualify new equipment for manufacturing processes and test methods
- Design and optimize process and process equipment for large and small scale manufacturing.
- Execute methods needed for efficient and effective process and test method development (design for manufacturing/assembly, process validation, process capability, lean manufacturing, equipment selection and qualification, and specification development).
- Generation of technical documentation associated with equipment. (schematics/drawings/User Manuals)
- Hold equipment design review meetings to agree on feasible solutions.
- Manage Vendors for delivery of build components.
- The integration of machined components with off the shelf parts to complete the equipment. (Keeping spares to a minimum)
- Generation of the specification for any components required within the equipment, i.e. PLCs, Sensors, Pneumatic Actuators, and Servo Motors etc.
- The manufacture of components as per the supplied drawings, with emphasis on machining fits and tolerances.
- The integration of electrical components. (HMI/PLC/Loadcell/sensors etc)
- The integration of any pneumatic components into the equipment. (Cylinders/regulators etc)
- Integration of Safety components as part of in-house CE marking. This includes safety relays, safety interlock switches, safety sensors, etc.
- The programming and debugging of equipment PLC.
- Assisting New Product Introduction Team to introduce new equipment into manufacturing.
- Support installation and maintenance of the equipment.
- Research of new automation/control technologies for implementation into new and existing equipment.
- Provide technical support for the equipment build during build and debug of the equipment once complete.
- Liaise and communicate with the other project team members.
- Ability to complete projects within specific timelines and meeting performance expectations.
- Adhere to the Quality Management System and its processes to meet FDA 21 CFR 820, ISO 13485, and other applicable regulatory requirements.
Qualifications
Requirements:
- Bachelors degree in Engineering required
- Minimum of 5 years’ relevant experience is required.
- Ability to use machine shop equipment (milling machines, lathes etc) is an advantage.
- Ability to use a 3D Cad package such as Creo/Solidworks is required.
- Knowledge of CE marking standards, preferred.
- Knowledge of medical device quality standards/practices or similar regulated industry.
- Good communication and inter-personal skills.
- Proven problem-solving skills and High self-motivation.
- Good computer skills including knowledge of Microsoft® Office.
- Organizational and team building skills.
Physical Requirements:
- Works under general office environment conditions.- Utilizes close visual acuity for working with computers and equipment.- Frequently required to sit, stand, walk, and communicate.
- Must be able to perform the essential functions of the job, subject to reasonable accommodation requirements under the ADA.
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