Binny's Beverage DepotNorthbrook
Demonstrates supervisory and training/coaching skills. Perform all duties as assigned by supervisors. ...
ESPO CorporationVernon Hills, 3 mi from Mundelein
Maintenance Mechanic
Permanent/Direct Hire
Vernon Hills, IL
3rd shift/night shift: Rotating 12-hour shift, they work 2 on 2 off 3 on 3 off from 6:00pm - 6:00 am. Must be available on alternating weekends and some holidays.
Job Overview:
Our...
NemeraBuffalo Grove, 7 mi from Mundelein
Job Description
Position Purpose: The Maintenance Technician – Auxiliary is responsible for monitoring, troubleshooting, and repairs on various types of auxiliary equipment and auxiliary molding support equipment.
KEY RESPONSIBILITIES/ESSENTIAL...
AbbVieNorth Chicago, 9 mi from Mundelein
Job Description
The Maintenance Technician III will work independently, providing technical support within the maintenance department as well as training junior technicians on more complex tasks. The work hours for this technician...
Penske Truck LeasingElk Grove Village
Automotive, Diesel, Diesel Repair, Diesel Tech, Diesel Mechanic, Gas Mechanic, Mechanic, Hydraulics Auto Repair, Truck Repair, Trailer Repair, Equipment Installer, Electronic Diagnostic, Car Carrier Repair, Mechanical Repair, Installer, Truck Equipment, Auto Mechanic, ASE Certified, ASE, Automotive,...
Advanced Technology ServicesBartlett
We are professionals in Industrial Maintenance and we make factories run better. Performs entry to mid-level break-fix & preventative maintenance. Is aware of Maintenance Industry Standards. ...
Aegis WorldwideMundelein
itle: 3rd shift Maintenance Supervisor - Food Mfg clinet
Mundelein, IL
Benefits Offered
• Dental, Life, Medical, Paid Time Off, Retirement, Vision
Description:
The shifts will be 12-hour shifts with 3 1/2-day work weeks and alternating weekends...
LHHLincolnshire (IL), 7 mi from Mundelein
LHH Recruitment Solutions has partnered with a growing organization, and they are seeking a highly motivated Maintenance Technician / Technical Operator to join their team in Lincolnshire, IL. The ideal candidate will possess a strong background...
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Validation Engineer | Medical Device | Mundelein, IL
Michael Page | Mundelein | $90,000/year | michaelpage.com |
About Our Client
Our client is a medical device manufacturer located in the Wheeling area. With over 15 locations throughout the US and 5000 employees, they have continued to grow out new product lines. They seek a Validation Engineer to join their Quality team.
Their clients include well known OEMs, such as Stryker and Medtronic. This role will be responsible for all customer communication, root cause/corrective actions and leading floor initiatives to increase efficiency.
Job Description
The Quality Engineer will be responsible for;
• Supports regulatory and agency inspections, audits, investigations, and inquiries regarding the control and assessment of product design and manufacturing quality.
• Leads and implements various product and process improvement methodologies.
• Review the adequacy and correctness of changes to Bill of Materials (BOM's), Assembly Procedures, Drawings, Component Specification, FMEAs, Control Plans, etc.
• Leads in the completion and maintenance of risk analysis.
• Leads generation and completion of protocols and reports for test method validations.
• Interfaces with Manufacturing Engineers to review processes for new and existing products and coordinate process validations and capability studies. Recommends process monitoring devices where applicable.
• Develops various inspection techniques and procedures to ensure product integrity to design specifications. Responsible for the writing, approval and implementation of Incoming, In-Process and Final Inspection procedures.
• Ensures that the disposition of non-conforming materials meet all necessary regulatory requirements and assure adequacy of corrective actions to prevent re-occurrence.
Additional Responsibilities:
• Acts as a lead in plant CAPA activities, including analysis of data and trends in complaints, supplier quality, nonconforming material, training effectiveness, and root causes analysis.
• Works with suppliers, management, Engineers and Manufacturing associates in the resolution of quality problems. Also, leads each of these groups with capability studies and the application of statistical quality control which include Cpk, DOE, Hypotheses Testing, etc.
• Coordinates and leads the preparation of Quality Plans, including inspection, test and gauge requirements for new product introductions
• Provides support to other quality engineers.
• Performs other functions as required.
MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law.
MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.
The Successful Applicant
• Bachelor's Degree (Engineering related), Master's Degree preferred
• 4+ years of experience in a manufacturing environment, specifically in metal working or medical device manufacturing preferred
• Project Management and Lean Manufacturing experience
• Good knowledge of statistical tool sand appropriate use of Design of Experiments (DOE) when developing recommendations
• Excellent communication and interpersonal skills
• Working knowledge of ISO 9001:2015, ISO 13485:2015, 21 CFR and cGMPs
What's on Offer
• Competitive base salary between $85,000-$90,000, depending on experience and skills
• Bonus opportunity up to 5%
• Comprehensive benefits package including Medical, Dental and Vision
• Medical/Prescription Drug Coverage - 3 Blue Cross Option (2 PPOs, 1 HDHP)
• Health Savings Account and Flexible Spending Accounts
• Dental Coverage - 2 Met Life Options
• Life and AD&D Coverage
• Short-term disability coverage
• 15 PTO Days + 10 holidays
• 401(k) with 3% company match
Additional Benefits
• Pet Insurance
• Tuition Reimbursement
Our client is a medical device manufacturer located in the Wheeling area. With over 15 locations throughout the US and 5000 employees, they have continued to grow out new product lines. They seek a Validation Engineer to join their Quality team.
Their clients include well known OEMs, such as Stryker and Medtronic. This role will be responsible for all customer communication, root cause/corrective actions and leading floor initiatives to increase efficiency.
Job Description
The Quality Engineer will be responsible for;
• Supports regulatory and agency inspections, audits, investigations, and inquiries regarding the control and assessment of product design and manufacturing quality.
• Leads and implements various product and process improvement methodologies.
• Review the adequacy and correctness of changes to Bill of Materials (BOM's), Assembly Procedures, Drawings, Component Specification, FMEAs, Control Plans, etc.
• Leads in the completion and maintenance of risk analysis.
• Leads generation and completion of protocols and reports for test method validations.
• Interfaces with Manufacturing Engineers to review processes for new and existing products and coordinate process validations and capability studies. Recommends process monitoring devices where applicable.
• Develops various inspection techniques and procedures to ensure product integrity to design specifications. Responsible for the writing, approval and implementation of Incoming, In-Process and Final Inspection procedures.
• Ensures that the disposition of non-conforming materials meet all necessary regulatory requirements and assure adequacy of corrective actions to prevent re-occurrence.
Additional Responsibilities:
• Acts as a lead in plant CAPA activities, including analysis of data and trends in complaints, supplier quality, nonconforming material, training effectiveness, and root causes analysis.
• Works with suppliers, management, Engineers and Manufacturing associates in the resolution of quality problems. Also, leads each of these groups with capability studies and the application of statistical quality control which include Cpk, DOE, Hypotheses Testing, etc.
• Coordinates and leads the preparation of Quality Plans, including inspection, test and gauge requirements for new product introductions
• Provides support to other quality engineers.
• Performs other functions as required.
MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law.
MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.
The Successful Applicant
• Bachelor's Degree (Engineering related), Master's Degree preferred
• 4+ years of experience in a manufacturing environment, specifically in metal working or medical device manufacturing preferred
• Project Management and Lean Manufacturing experience
• Good knowledge of statistical tool sand appropriate use of Design of Experiments (DOE) when developing recommendations
• Excellent communication and interpersonal skills
• Working knowledge of ISO 9001:2015, ISO 13485:2015, 21 CFR and cGMPs
What's on Offer
• Competitive base salary between $85,000-$90,000, depending on experience and skills
• Bonus opportunity up to 5%
• Comprehensive benefits package including Medical, Dental and Vision
• Medical/Prescription Drug Coverage - 3 Blue Cross Option (2 PPOs, 1 HDHP)
• Health Savings Account and Flexible Spending Accounts
• Dental Coverage - 2 Met Life Options
• Life and AD&D Coverage
• Short-term disability coverage
• 15 PTO Days + 10 holidays
• 401(k) with 3% company match
Additional Benefits
• Pet Insurance
• Tuition Reimbursement