Binny's Beverage DepotWaukegan
Assist in developing sales, maintaining productivity levels and providing superior customer service, while ensuring the safety and cleanliness of the store.Work as part of a team, following the directions of managers and supervisors, while adhering to the policies and procedures explained in the Emp...
WALGREENSDeerfield (IL), 6 mi from Buffalo Grove
function, and may include responsibilities in the area of Security, Planning anda Analysis, Strategy or Operations, such as:
• Developing and executing assigned high profile plans/programs to enhance/maximize consumer awareness, market share and support...
Artech LLCRiverwoods, 3 mi from Buffalo Grove
Title: RPA Analyst
Location: 2500 Lake Cook Road, Riverwoods, Illinois, 60015
Job ID: 7126
JOB DESCRIPTION
Serve as the Analyst that works with business partners and developers to automate processes based on requirements. Primary software...
MAT Holdings, IncLong Grove (IL), 2 mi from Buffalo Grove
Job Description
The Sr. Logistics Sourcing Analyst will lead Carrier Development and Sourcing Projects across North American Spend Categories for MAT Holdings business units. The ideal candidate for this role will demonstrate a high level...
MAT Holdings, IncLong Grove (IL), 2 mi from Buffalo Grove
Job Description
The role of Treasury & Risk Management analyst will be responsible for the day-to-day treasury and insurance related functions for MAT Holdings, Inc. (the Company). Treasury responsibilities include facilitating bank activities...
Jackson Therapy PartnersVilla Park
Join our client's team as a licensed Physical Therapist for a full time position with a mission driven facility where expert therapy professionals help patients with injuries and illnesses improve their movement, manage their pain, and prevent loss of mobility.Bachelor's, Master's or Doctoral Degree...
Medline Industries LPMundelein, 7 mi from Buffalo Grove
WORK EXPERIENCE
%26bull; 5+ years of data, business and/or systems analyst experience to include translating between business and technical requirements.
%26bull; Multiple SAP project implementations and rollouts
Understanding of SAP ECC platform...
LaSalle NetworkHoffman Estates, 6 mi from Buffalo Grove
revenue growth or expense saving projects/ opportunities
• Apply financial analysis to create presentation material for leadership meetings, and department strategy meetings
• Provide guidance and coaching to Product Managers on techniques and best...
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Manufacturing Engineering Manager
Michael Page | Buffalo Grove | $150,000/year | michaelpage.com |
About Our Client
Our client is a global contract medical device manufacturer, with over 20 locations throughout North America. They seek an experienced Engineering Manager, that will oversee their Sustaining Engineering Team and report to the Director of Operations.
Their customers include well known OEMs, such as Stryker, Medtronic and Smith & Nephew.
This site is one of their largest in the Midwest, with over 200 employees and 3 buildings. The site is known for their culture, leadership team and stability. This person will oversee a team of 9 full-time employees, including Engineers and Technicians and work cross-functionally with Production, Quality and Operations.
Job Description
This role will be responsible for managing a team of engineers and technicians focused on sustaining engineering activities, including product improvements, cost reduction initiatives, quality enhancements, and regulatory compliance.
• Lead and mentor a team of engineers and technicians responsible for sustaining engineering activities. Foster a culture of collaboration, innovation, and continuous improvement within the team.
• Oversee all aspects of sustaining engineering projects, including planning, execution, and monitoring. Prioritize projects based on strategic objectives, customer needs, and regulatory requirements
• Drive continuous improvement initiatives to enhance the performance, reliability, and manufacturability of existing medical devices. Work closely with cross-functional teams, including R&D, Quality, and Operations, to implement design changes effectively.
• Identify opportunities for cost reduction through value engineering, process optimization, and supplier management. Develop and implement strategies to achieve cost reduction targets without compromising product quality or regulatory compliance.
• Collaborate with the Quality team to ensure compliance with regulatory standards and industry best practices. Lead investigations into product quality issues, implement corrective and preventive actions, and drive root cause analysis efforts.
• Maintain a thorough understanding of regulatory requirements applicable to medical devices. Ensure that all sustaining engineering activities comply with FDA regulations, ISO standards, and other relevant regulatory frameworks.
• Partner with cross-functional teams, including Sales, Marketing, and Customer Support, to address customer feedback, support product launches, and drive customer satisfaction.
• Ensure accurate and timely documentation of all sustaining engineering activities, including design changes, test protocols, and validation reports. Provide regular progress updates and reports to senior management.
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 in Engineering or related field; advanced degree preferred.
• 10+ years of Manufacturing experience, with 5+ years in Engineering leadership roles
• Medical device manufacturing experience is preferred
• Proven track record of successfully managing engineering teams and delivering results in a fast-paced, regulated environment
• In-depth knowledge of medical device regulations, including FDA QSR, ISO 13485, and MDD/MDR
• Strong understanding of design control processes, risk management principles, and quality systems
• Excellent communication, interpersonal, and leadership skills
• Demonstrated ability to drive cross-functional collaboration and influence stakeholders at all levels of the organization
What's on Offer
• Base salary between $130,000-$150,000, depending on experience and skills
• Bonus opportunity up to 15%, based on site performance, team and individual metrics
• Estimated total package circa $175,000
• 17 Days of Paid Vacation + 10 holidays
• 401(k) with 3% company match
• Comprehensive Medical, Dental and Vision Insurance Options - Employees are eligible on first day of employement
• Medical/Prescription Drug Coverage - 3 Blue Cross Options (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
• Tuition Reimbursement
Our client is a global contract medical device manufacturer, with over 20 locations throughout North America. They seek an experienced Engineering Manager, that will oversee their Sustaining Engineering Team and report to the Director of Operations.
Their customers include well known OEMs, such as Stryker, Medtronic and Smith & Nephew.
This site is one of their largest in the Midwest, with over 200 employees and 3 buildings. The site is known for their culture, leadership team and stability. This person will oversee a team of 9 full-time employees, including Engineers and Technicians and work cross-functionally with Production, Quality and Operations.
Job Description
This role will be responsible for managing a team of engineers and technicians focused on sustaining engineering activities, including product improvements, cost reduction initiatives, quality enhancements, and regulatory compliance.
• Lead and mentor a team of engineers and technicians responsible for sustaining engineering activities. Foster a culture of collaboration, innovation, and continuous improvement within the team.
• Oversee all aspects of sustaining engineering projects, including planning, execution, and monitoring. Prioritize projects based on strategic objectives, customer needs, and regulatory requirements
• Drive continuous improvement initiatives to enhance the performance, reliability, and manufacturability of existing medical devices. Work closely with cross-functional teams, including R&D, Quality, and Operations, to implement design changes effectively.
• Identify opportunities for cost reduction through value engineering, process optimization, and supplier management. Develop and implement strategies to achieve cost reduction targets without compromising product quality or regulatory compliance.
• Collaborate with the Quality team to ensure compliance with regulatory standards and industry best practices. Lead investigations into product quality issues, implement corrective and preventive actions, and drive root cause analysis efforts.
• Maintain a thorough understanding of regulatory requirements applicable to medical devices. Ensure that all sustaining engineering activities comply with FDA regulations, ISO standards, and other relevant regulatory frameworks.
• Partner with cross-functional teams, including Sales, Marketing, and Customer Support, to address customer feedback, support product launches, and drive customer satisfaction.
• Ensure accurate and timely documentation of all sustaining engineering activities, including design changes, test protocols, and validation reports. Provide regular progress updates and reports to senior management.
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 in Engineering or related field; advanced degree preferred.
• 10+ years of Manufacturing experience, with 5+ years in Engineering leadership roles
• Medical device manufacturing experience is preferred
• Proven track record of successfully managing engineering teams and delivering results in a fast-paced, regulated environment
• In-depth knowledge of medical device regulations, including FDA QSR, ISO 13485, and MDD/MDR
• Strong understanding of design control processes, risk management principles, and quality systems
• Excellent communication, interpersonal, and leadership skills
• Demonstrated ability to drive cross-functional collaboration and influence stakeholders at all levels of the organization
What's on Offer
• Base salary between $130,000-$150,000, depending on experience and skills
• Bonus opportunity up to 15%, based on site performance, team and individual metrics
• Estimated total package circa $175,000
• 17 Days of Paid Vacation + 10 holidays
• 401(k) with 3% company match
• Comprehensive Medical, Dental and Vision Insurance Options - Employees are eligible on first day of employement
• Medical/Prescription Drug Coverage - 3 Blue Cross Options (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
• Tuition Reimbursement
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