Senior Manufacturing Process Engineer

Full-time

The Opportunity

This position is an onsite opportunity in the Abbott Diabetes Care Division. We are helping people with Diabetes lead healthier, happier lives.

As a global leader in diabetes care, Abbott is constantly working to deliver the highest quality products and unwavering support to our customers.

Consistent and accurate glucose monitoring is the foundation of any diabetes management plan, so we’re committed to continuous improvement in the way patients and professionals measure, track and analyze glucose levels

As a Senior Manufacturing Process Engineer, you will be responsible for providing subject matter expect software support for wider ranging manufacturing processes into Third Party Manufacturing facility.

Participates in design, planning and support of the introduction of high speed automation lines into Third party manufacturing facility.

The position provides technical leadership in areas of PLC communications, vision and RFID communications while driving activities at the supplier(s) to ensure automation & software support is available to scale up to increased volumes are achieved within ADC requirements.

This is an onsite opportunity in Buffalo Grove, IL or Austin, TX.

What You'll Do

  • Independently design and lead complex engineering studies and experiments often with multiple variables.
  • Analyze complex problems and identify their impact. establish probabilities. draw conclusions reflecting broad business needs.

set complex design and process requirements.

  • Responsible for completing documentation in a timely manner and in accordance with business standards.
  • Lead and / or participate on cross-functional teams to support organizational goals.
  • Other tasks and duties as assigned.
  • Understand and comply with applicable EHS policies, procedures, rules and regulations.

Experience You'll Bring

Required :

  • Bachelors in Electrical or Computer Science or related engineering or scientific field.
  • MS or PhD degree ideal.
  • 6 years relevant experience and a Bachelor’s degree or 4 yrs with MS Good knowledge of software engineering principles.
  • Excellent written and verbal communication skills are essential.
  • Minimum 4 years of experience (such as software design, coding

Preferred :

  • Expert knowledge on PLC programming with Allen Bradley controls systems
  • Expert knowledge of Cognex vision systems
  • Working knowledge of RFID communications
  • Experience in generation / execution of software test plans
  • Experience in FAT, SAT, commissioning & validation of high-speed automation equipment.
  • Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan. Free cov erage applies in the next calendar year.

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life.

Abbott is an Equal Opportunity Employer, committed to employee diversity.

Divisional Information

Medical Devices

General Medical Devices :

Our medical devices help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than 500,000 people with diabetes from routine fingersticks.

As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats.

Diabetes

We’re focused on helping people with diabetes manage their health with life-changing products that provide accurate data to drive better-informed decisions.

We’re revolutionizing the way people monitor their glucose levels with our new sensing technology.

Vascular

Abbott Vascular provides innovative, minimally invasive, and cost-effective products for treatment of vascular disease.

Neuromodulation

Our Neuromodulation business includes implantable devices compatible with mobile technology to help people who suffer from chronic pain and movement disorders.

These non-opioid therapies allow us to provide interventional pain therapy to patients throughout the pain continuum.

Structural Heart

Structural Heart Business Mission : why we exist

Our business purpose is to restore health and improve quality of life through the design and provision of device and management solutions for the treatment of structural heart disease.

In Abbott’s Electrophysiology (EP) business, we’re advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives.

In Abbott’s Heart Failure (HF) business, we’re developing solutions to diagnose, monitor and manage heart failure, allowing people to restore their health and get on with their lives.

Diagnostics

We’re empowering smarter medical and economic decision making to help transform the way people manage their health at all stages of life.

Every day, more than 10 million tests are run on

Abbott’s diagnostics instruments, providing lab results for millions of people.

Abbott Molecular is a leader in molecular diagnostics and the analysis of DNA, RNA, and proteins at the molecular level.

Our Point of Care diagnostic portfolio spans key heath and therapeutic areas, including infections disease, cardiometabolic, informatics and toxicology.

Our diagnostic solutions are used in hospitals, laboratories and clinics around the globe. The crucial information derived from our tests, instruments and informatics systems are often the first step in patient care decision making for hundreds of health conditions from heart attacks to blood disorders to infectious diseases and cancers.

Our rapid diagnostics solutions are helping address some of the world’s greatest healthcare challenges.

Nutrition

Our nutrition business develops science-based nutrition products for people of all ages, from helping babies and children grow, to keeping adult bodies strong and active.

Millions of people around the world count on our leading brands including Similac, PediaSure, Pedialyte, Ensure, Glucerna and ZonePerfect to help get the nutrients they need to live their healthiest life.

The base pay for this position is $80,700.00 $161,300.00. In specific locations, the pay range may vary from the range posted.

Apply Now

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Senior Manufacturing Process Engineer

abbot Chicago, IL
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The Opportunity

This position is an onsite opportunity in the Abbott Diabetes Care Division. We are helping people with Diabetes lead healthier, happier lives.

As a global leader in diabetes care, Abbott is constantly working to deliver the highest quality products and unwavering support to our customers.

Consistent and accurate glucose monitoring is the foundation of any diabetes management plan, so we’re committed to continuous improvement in the way patients and professionals measure, track and analyze glucose levels

As a Senior Manufacturing Process Engineer, you will be responsible for providing subject matter expect software support for wider ranging manufacturing processes into Third Party Manufacturing facility.

Participates in design, planning and support of the introduction of high speed automation lines into Third party manufacturing facility.

The position provides technical leadership in areas of PLC communications, vision and RFID communications while driving activities at the supplier(s) to ensure automation & software support is available to scale up to increased volumes are achieved within ADC requirements.

This is an onsite opportunity in Buffalo Grove, IL or Austin, TX.

What You'll Do

  • Independently design and lead complex engineering studies and experiments often with multiple variables.
  • Analyze complex problems and identify their impact. establish probabilities. draw conclusions reflecting broad business needs.

set complex design and process requirements.

  • Responsible for completing documentation in a timely manner and in accordance with business standards.
  • Lead and / or participate on cross-functional teams to support organizational goals.
  • Other tasks and duties as assigned.
  • Understand and comply with applicable EHS policies, procedures, rules and regulations.

Experience You'll Bring

Required :

  • Bachelors in Electrical or Computer Science or related engineering or scientific field.
  • MS or PhD degree ideal.
  • 6 years relevant experience and a Bachelor’s degree or 4 yrs with MS Good knowledge of software engineering principles.
  • Excellent written and verbal communication skills are essential.
  • Minimum 4 years of experience (such as software design, coding

Preferred :

  • Expert knowledge on PLC programming with Allen Bradley controls systems
  • Expert knowledge of Cognex vision systems
  • Working knowledge of RFID communications
  • Experience in generation / execution of software test plans
  • Experience in FAT, SAT, commissioning & validation of high-speed automation equipment.
  • Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan. Free cov erage applies in the next calendar year.

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life.

Abbott is an Equal Opportunity Employer, committed to employee diversity.

Divisional Information

Medical Devices

General Medical Devices :

Our medical devices help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than 500,000 people with diabetes from routine fingersticks.

As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats.

Diabetes

We’re focused on helping people with diabetes manage their health with life-changing products that provide accurate data to drive better-informed decisions.

We’re revolutionizing the way people monitor their glucose levels with our new sensing technology.

Vascular

Abbott Vascular provides innovative, minimally invasive, and cost-effective products for treatment of vascular disease.

Neuromodulation

Our Neuromodulation business includes implantable devices compatible with mobile technology to help people who suffer from chronic pain and movement disorders.

These non-opioid therapies allow us to provide interventional pain therapy to patients throughout the pain continuum.

Structural Heart

Structural Heart Business Mission : why we exist

Our business purpose is to restore health and improve quality of life through the design and provision of device and management solutions for the treatment of structural heart disease.

In Abbott’s Electrophysiology (EP) business, we’re advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives.

In Abbott’s Heart Failure (HF) business, we’re developing solutions to diagnose, monitor and manage heart failure, allowing people to restore their health and get on with their lives.

Diagnostics

We’re empowering smarter medical and economic decision making to help transform the way people manage their health at all stages of life.

Every day, more than 10 million tests are run on

Abbott’s diagnostics instruments, providing lab results for millions of people.

Abbott Molecular is a leader in molecular diagnostics and the analysis of DNA, RNA, and proteins at the molecular level.

Our Point of Care diagnostic portfolio spans key heath and therapeutic areas, including infections disease, cardiometabolic, informatics and toxicology.

Our diagnostic solutions are used in hospitals, laboratories and clinics around the globe. The crucial information derived from our tests, instruments and informatics systems are often the first step in patient care decision making for hundreds of health conditions from heart attacks to blood disorders to infectious diseases and cancers.

Our rapid diagnostics solutions are helping address some of the world’s greatest healthcare challenges.

Nutrition

Our nutrition business develops science-based nutrition products for people of all ages, from helping babies and children grow, to keeping adult bodies strong and active.

Millions of people around the world count on our leading brands including Similac, PediaSure, Pedialyte, Ensure, Glucerna and ZonePerfect to help get the nutrients they need to live their healthiest life.

The base pay for this position is $80,700.00 $161,300.00. In specific locations, the pay range may vary from the range posted.

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Value Engineer- Manufacturing + Production

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We're Celonis, the global leader in execution management and process mining technology, and one of the 50 most valuable private companies in the world.

We believe that every company can unlock its full execution capacity - and for that, we need you to join us.

The Role :

As a Value Engineer, you are spearheading our mission of data-driven business transformation with our customers. You will work in partnership with the Celonis Sales Teams and have full responsibility for the end-to-end value journey of our customers.

You are our customers trusted advisor and help them achieve their strategic goals and realize significant value using Celonis EMS.

In collaboration with our partners and Celonis Services, you will drive measurable business impact across various processes and industries and accelerate the adoption of our platform.

You will blend deep process and industry expertise with a proven consulting skill set with strong analytical skills at the forefront of one of the fastest-growing tech companies worldwide.

The work you’ll do :

Identify & Frame Value

  • Discover and translate customers’ strategic priorities into high-impact Celonis use cases
  • Build demos and business cases, leveraging industry benchmarks and best practices in order to win new customers
  • Undertake Value Assessments or Proof-of-Value Projects and communicate the value opportunity and strategic roadmap to C-Level executives

Realize Value

  • Facilitate business value workshops and use Celonis to identify and qualify opportunities for process enhancement
  • Derive improvement measures in core business functions and initiate improvement actions and enterprise-wide change initiatives
  • Present results and realized value to senior management and C-level executives

Scale Value

  • Responsible for the end-to-end customer value journey, landing, expanding, adoption and renewing
  • Build a strategic expansion roadmap for customers embedding Celonis EMS as a strategic business transformation platform in their organization and therefore drive adoption and expansion
  • Provide feedback to our product development teams to enhance the Celonis platform and Apps based on new use cases

The qualifications you need :

  • Value Selling Methodology : You have advanced knowledge and experience following the Celonis value selling methodology alongside the customer journey : including discovery, qualification, value assessment and PoV’s, and demonstrate the full value potential of Celonis EMS
  • Product Expertise : You are an expert in guiding the customer’s IT team throughout their EMS journey, demonstrating hands-on the power of EMS and accelerating value realization by building dashboards, Apps, Action Flows
  • Value Realization : You have advanced knowledge and expertise in identifying and prioritising use cases, implementing improvement measures and becoming a change agent for the customer by establishing an operating model and training users for the customer to realize value and renew / expand their subscription with Celonis
  • Project Management : You are able toplan and manage project scope, expectations and timelines. You will need to manage multiple projects across your aligned accounts that will be at different parts of the value journey.

Also, you will leverage partners from the Celonis Ecosystem wherever possible.

  • Executive Stakeholder Management : Proven experience in preparing and communicating results to stakeholders and management, both internally and externally.
  • Domain Expertise : Leverage your advanced business domain expertise, such as in Finance or Supply Chain as well as strategic transformation initiatives (e.

g. Shared Services Transformation or System Transformation) and build a compelling value roadmap for the customer

Industry Expertise : You have advanced industry expertise and a proven ability to develop a deep understanding of industry trends and strategic opportunities of the C-Suite and build an integrated Celonis EMS roadmap

What Celonis can offer you :

  • The unique opportunity to work within a new category of technology, Execution Management
  • Investment in your personal growth and skill development (clear career paths, internal mobility opportunities, L&D platform, mentorships, and more)
  • Great compensation and benefits packages (stock options, 401(k) matching, generous time off, family leave from day one, and more)
  • Mental well-being support (mindfulness tools such as Headspace, virtual events, and more)
  • A global and growing team of Celonauts from diverse backgrounds to learn from and work with
  • An open-minded culture with innovative, autonomous teams
  • Business Resource Groups to help you feel connected, valued and seen ([email protected], [email protected], [email protected], [email protected], [email protected], and more)
  • A clear set of that guide everything we do : Live for Customer Value, The Best Team Wins, We Own It, and Earth Is Our Future

About Us

Celonis reveals and fixes inefficiencies businesses can’t see, enabling them to perform at levels they never thought possible.

Powered by its market-leading process mining core, the Celonis Execution Management System provides a full set of platform capabilities for business executives and users to eliminate billions in corporate inefficiencies, provide better customer experience and reduce carbon emissions.

Celonis has thousands of implementations with global customers and is headquartered in Munich, Germany and New York City, USA with more than 23 offices worldwide.

Celonis is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment and equal opportunity in all aspects of employment.

We will not tolerate any unlawful discrimination or harassment of any kind. We make all employment decisions without regard to race / ethnicity, color, sex, pregnancy, age, sexual orientation, gender identity or expression, transgender status, national origin, citizenship status, religion, physical or mental disability, veteran status, or any other factor protected by applicable anti-discrimination laws.

As a US federal contractor, we are committed to the principles of affirmative action in accordance with applicable laws and regulations.

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Manufacturing Engineer II

TALIS Chicago, IL
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About the Company

Our purpose at Talis Biomedical is to advance health equity and outcomes by delivering accurate infectious disease testing in the moment of need, at the point of care.

While timely diagnosis of infectious diseases is critically important to enable effective treatment, testing is primarily performed in centralized laboratories, which require samples to be shipped for processing, delaying the return of results by days.

Point-of-care testing solves this problem by delivering the timely information necessary for clinical care.

To deliver our purpose we focus on three things :

  • Putting customers and patients first
  • Making Talis a great place to work
  • Living our values to Dream Big, Share Our Screens, Serve Others, Bring Our A Game, and Build Trust

Job Title : Manufacturing Engineer II Division / Department : Operations Manufacturing Engineering Reports to : Senior Manager of Manufacturing Engineering Date : May 2023 Position Summary This position will report to a Sr.

Manager Manufacturing Engineer and will be responsible for developing, documenting, and validating manufacturing processes for an IVD Consumable.

Specific responsibilities include, but are not limited to :

  • Develop and control efficient manufacturing processes for assembly of a microfluidic cartridge containing injection molded components, wet and dry reagents, and a wide range of assembly processes.
  • Own and maintain design and process documentation including Item Specification, Process Instructions, BOM, Drawings, etc.

Perform change management, including creation and routing of change orders, identifying appropriate process impacts, risks, and justification for change.

  • Assist in identifying and procuring manufacturing equipment ranging from custom large-scale PLC / PC -based automation equipment to small fixturing.
  • Own, plan and execute design transfer activities, including validation of equipment and processes, requirements creation, Master Validation Plans, IQ / OQ / PQ Protocols and Reports, Test Method Validation, Process Flow Diagrams, pFMEA, etc.
  • Transfer manufacturing processes to internal and external suppliers, collaborating effectively across functions to meet various customer needs, including appropriate training.
  • Lead cost reduction, capacity scaling, and quality improvement activities (equipment and manpower) to meet business needs.
  • Participate in CAPA investigations, NCM resolution, failure and root-cause analysis, and other investigation activities.
  • Ensure compliance to Quality System Requirements within an FDA regulated manufacturing environment.
  • Leverage a strong understanding of manufacturing metrics to appropriately select process indicators that quickly and effectively communicate product and process health.
  • May be asked to support pilot manufacturing on automation system, or other tasks as required by the company.
  • Mentor junior engineers.

Education / Skills / Requirements

  • BS / MS degree in Mechanical Engineering or equivalent.
  • 3 - 5 years of experience in FDA regulated product development or manufacturing desired.
  • Excellent communication, organization, follow-up, and documentation skills.
  • Strong problem-solving skills.
  • CAD experience (Solidworks preferred).

Talis Biomedical offers a comprehensive health and well-being benefits programs, long-term equity incentives, time-off policies, a 401(k) retirement savings plan with an immediate Company match, Education Assistance Program, a rotating suite of snacks, Happy Hours, office perks, and other fun company events! Best of all, join us by working at a growing company like Talis with dedicated and collaborative employees committed to making a difference in Health Care.

Talis Biomedical is proud to be an equal opportunity workplace. All aspects of employment decisions will be based on merit, competence, performance, and business needs.

We do not discriminate on the basis of any status protected under federal, state, or local law. We celebrate diversity and are committed to creating an inclusive environment for our colleagues.

Talis Biomedical is an E-Verify Participation company.

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Senior Manufacturing Engineer

ESPO Corporation Chicago, IL
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Job Title : Sr. Manufacturing Engineer

Location : Chicago Heights, IL

Job Type and Duration : Direct Hire

Pay rate : Flexible

Summary :

Hands-on engineer to lead the analysis of production problems, establish and improve manufacturing methods and address equipment and tooling needs to reduce costs and improve product quality within our fast paced sheet metal fabrication environment

Job Description :

  • Troubleshoot and analyze manufacturing problems and implement corrective actions for high quality, efficient manufacturing solutions.
  • Analyze workflow, work methods, plant and department layouts for improved product flow in production.
  • Identify tools, jigs and fixtures, or other new or special equipment required for new production or improvements to existing production lines.
  • Design parts and fixtures utilizing solidworks and aid in fabrication
  • Practice Lean Methodology to eliminate waste and drive continuous process improvement opportunities to promote safety, quality, efficiency, and effectiveness
  • Investigate, analyze and prepare justifications for the purchase of manufacturing equipment. Obtain quotations from vendors;

submit capital appropriation requests for the purchase of specific equipment.

  • Collaborate with the Maintenance and Production teams on the installation and debugging of equipment.
  • Develop and maintain product routings.
  • Develop visual and written work guidelines.
  • Perform other manufacturing engineering tasks as assigned.

Qualifications :

  • Bachelor Degree in Manufacturing or Mechanical Engineering
  • Background in Sheet Metal manufacturing
  • Experience designing in Solidworks
  • Metal fabrication experience; welding and machining fixtures, lazer cutting, brake press operation. PEM Inserting machine a plus
  • Experience programming robotic welding equipment
  • Excellent communication, project management and organizational skills from the production floor up
  • Superior analytical and problem solving skills in a quick changing manufacturing environment
  • Knowledge of quick changeovers for short runs
  • 10-15 years working as a Manufacturing Engineer in a fabrication environment

ESPO Corporation

www.espocorp.com

View all open jobs at www.espocorp.com / jobs

Leaders in Technical Recruiting & Staffing since 1965

We are an Equal Opportunity Employer and value the benefits of diversity in our workforce . All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity and expression, national origin, disability, protected Veteran status, or any other attribute or protected characteristic by law.

If you need assistance applying please contact us directly.

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Manufacturing Engineer 3

Cantel Medical Chicago, IL
APPLY

Description :

At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe.

Position Summary

The Manufacturing Engineer will provide manufacturing engineering support to operations through line support, continuous improvement, capacity improvements and new product transfers.

You will help improve the overall efficiency of the manufacturing operation while optimizing human work factors, quality control, material flow, etc.

by identifying areas for improvement through use of statistics and root cause analysis tools.

Duties

  • Prepares straightforward plans, designs, calculations, analyses, etc. in accordance with established codes, standards, drawings, or other specifications.
  • Conducts tests, gathers and analyzes information, helps interpret findings.
  • Requires familiarity with technical terms or procedures basic to the function in order to communicate effectively with co-workers.
  • Requires basic oral, written and listening skills to gather, prepare, present and discuss findings and conclusions.
  • Create and maintain BOMs and routers following accepted standards and ensuring a high degree of accuracy.
  • Performs engineering calculations by calculator or computer to solve routine engineering problems.
  • Participate as a member of the product development team; interact with interdisciplinary teams in various projects.
  • Assists in the development of engineering drawings and specifications.
  • Assists in the design and fabrication of manufacturing process equipment and methods.
  • Assists in the troubleshooting of systems and equipment and performs repairs under close supervision.
  • Requisitions components and supplies for engineering projects, interacting with vendors to obtain price and product information.
  • Performs manufacturability studies on new product designs.
  • Works closely with Design Engineering during the manufacturability studies.

Education Degree

Bachelor's Degree in Engineering General

Required Experience

Bachelor’s degree in Engineering (any) or related field of study AND Five (5) Years of experience in the job offered or related occupation in which the required experience was gained.

In lieu of a Bachelor’s degree in Engineering (any) or related field of study AND Five (5) Years of experience, the employer will also accept a Master’s degree in Engineering (any) or related field of study AND Two (2) Years of experience in the job offered or related occupation in which the required experience was gained.

Must also have demonstrated experience with :

  • Part manufacturing, machine setup and part programming required in manufacturing process development;
  • Conducting quality internal audits (ISO 9001 : 2015);
  • Solid Works, Microsoft Excel, Auto CAD or Part Maker;
  • G code programming-manual and using CAM software;
  • Tooling applications (speed and feeds);
  • GDT;
  • Part tolerances;
  • Programming and machining at a precision machine shop;
  • CNC programming software (Solidworks or Partmaker);
  • Multi-axis CNC lathes, Swiss type CNC lathes, or vertical machining centers;
  • Using and reading various measuring instruments.

STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention.

WE HELP OUR CUSTOMERS CREATE A HEALTHIER AND SAFER WORLD by providing innovative healthcare, life sciences and dental products and services.

STERIS is a $5 billion, publicly traded (NYSE : STE) company with approximately 17,000 associates and Customers in more than 100 countries.

If you need assistance completing the application process, please call 1 (440) 392.7047. This contact information is for accommodation inquiries only and cannot be used to check application status.

STERIS is an Equal Opportunity Employer. We are committed to equal employment opportunity and the use of affirmative action programs to ensure that persons are recruited, hired, trained, transferred and promoted in all job groups regardless of race, color, religion, age, disability, national origin, citizenship status, military or veteran status, sex (including pregnancy, childbirth and related medical conditions), sexual orientation, gender identity, genetic information, and any other category protected by federal, state or local law.

We are not only committed to this policy by our status as a federal government contractor, but also we are strongly bound by the principle of equal employment opportunity.

The full affirmative action program, absent the data metrics required by 60-741.44(k), shall be available to all employees and applicants for employment for inspection upon request.

The program may be obtained at your location’s HR Office during normal business hours.

Full-time
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