manufacturing process engineer

<div>
 
 Job Description
 
 
 
 
 Manufacturing Process Engineer
 
 
 
 
 Collaborate with Innovative 3Mers Around the World
 
 
 
 Choosing where to start and grow your career has a major impact on your professional and personal life, so it&rsquo;s equally important you know that the company that you choose to work at, and its leaders, will support and guide you. With a wide variety of people, global locations, technologies and products, 3M is a place where you can collaborate with other curious, creative 3Mers.
 
 
 
 This position provides an opportunity to transition from other private, public, government or military experience to a 3M career.
 
 
 
 
 The Impact You&rsquo;ll Make in this Role
 
 
 
 As a Manufacturing Process Engineer, You Will Have The Opportunity To Tap Into Your Curiosity And Collaborate With Some Of The Most Innovative People Around The World. Here, You Will Make An Impact By
 
 
 
 <ul>
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 Providing technical leadership of assigned areas and function as subject matter expert in cellulose/chemical processes for the plant.
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 Being responsible for initiating and conducting broadly defined technical tasks and programs related to safety improvement, process improvement, cost reduction and other improvement initiatives. This includes driving capital investments, new product introductions and new technologies to increase manufacturing capability.
 </li>
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 Establishing and cultivating a network of support (EHS, laboratory, quality, plant engineering, business supply chain, engineering, etc..) to facilitate completion of assignments and performance of assigned areas.
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 Utilizing all data resources available to identify and drive the largest opportunities for assigned areas.
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 Enhance plant PPU in cellulose manufacturing to improve and sustain production of high-quality products and Overall Equipment Effectiveness.
 </li>
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 Managing documentation to include work instructions, process standards, technical documents, etc.
 </li>
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 Serve as a coach/mentor for technical resources.
 
 
 
 </li>
 </ul>
 
 Your Skills And Expertise
 
 
 
 To set you up for success in this role from day one, 3M requires (at a minimum) the following qualifications:
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree (completed and verified prior to start) from an accredited institution.
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 One (1) year of professional/intern experience as a process/manufacturing engineer, project engineer, or reliability engineer in a private, public, government or military environment.
 
 
 
 </li>
 </ul>
 Additional qualifications that could help you succeed even further in this role include:
 
 
 
 <ul>
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 Experience in a chemical, textile, paper or similar manufacturing environment.
 </li>
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 Experience with chemically processing rayon or cellulose derivatives.
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 Working knowledge and experience designing and troubleshooting process equipment including pumps, heat exchangers, and reactors.
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 Ability to complete material and energy balances and perform process optimization studies.
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 Ability to understand and interpret analytical chemical test results.
 </li>
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 Experience with statistical analysis of process data and establishing process control standards.
 </li>
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 Familiarity with PHA validations and change management processes.
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 Demonstrated ability to be a self-starter and strong influencing skills for working in dynamic plant environment.
 
 
 
 </li>
 </ul>
 
 Work location: Tonawanda, NY
 
 
 
 
 Travel: May include up to 10% domestic/international
 
 
 
 
 Relocation Assistance: May be authorized
 
 
 
 
 Must be legally authorized to work in country of employment without sponsorship for employment visa status (e.g., H1B status).
 
 
 
 
 Supporting Your Well-being
 
 
 
 3M offers many programs to help you live your best life &ndash; both physically and financially. To ensure competitive pay and benefits, 3M regularly benchmarks with other companies that are comparable in size and scope.
 
 
 
 Chat with Max
 
 
 
 For assistance with searching through our current job openings or for more information about all things 3M, visit Max, our virtual recruiting
 
 
 Applicable to US Applicants Only:The expected compensation range for this position is $98,413 - $120,282, which includes base pay plus variable incentive pay, if eligible. This range represents a good faith estimate for this position. The specific compensation offered to a candidate may vary based on factors including, but not limited to, the candidate&rsquo;s relevant knowledge, training, skills, work location, and/or experience. In addition, this position may be eligible for a range of benefits (e.g., Medical, Dental &amp; Vision, Health Savings Accounts, Health Care &amp; Dependent Care Flexible Spending Accounts, Disability Benefits, Life Insurance, Voluntary Benefits, Paid Absences and Retirement Benefits, etc.). Additional information is available at: https://www.3m.com/3M/en_US/careers-us/working-at-3m/benefits/.
 
 
 Good Faith Posting Date Range 11/04/2025 To 12/04/2025 Or until filled
 
 
 All US-based 3M full time employees will need to sign an employee agreement as a condition of employment with 3M. This agreement lays out key terms on using 3M Confidential Information and Trade Secrets. It also has provisions discussing conflicts of interest and how inventions are assigned. Employees that are Job Grade 7 or equivalent and above may also have obligations to not compete against 3M or solicit its employees or customers, both during their employment, and for a period after they leave 3M.
 
 
 Learn more about 3M&rsquo;s creative solutions to the world&rsquo;s problems at www.3M.com or on Instagram, Facebook, and LinkedIn @3M.
 
 
 Responsibilities of this position include that corporate policies, procedures and security standards are complied with while performing assigned duties.
 
 
 Safety is a core value at 3M. All employees are expected to contribute to a strong Environmental Health and Safety (EHS) culture by following safety policies, identifying hazards, and engaging in continuous improvement.
 
 
 Pay &amp; Benefits Overview: https://www.3m.com/3M/en_US/careers-us/working-at-3m/benefits/
 
 
 3M does not discriminate in hiring or employment on the basis of race, color, sex, national origin, religion, age, disability, veteran status, or any other characteristic protected by applicable law.
 
 
 
 Please note: your application may not be considered if you do not provide your education and work history, either by: 1) uploading a resume, or 2) entering the information into the application fields directly.
 
 
 
 
 3M Global Terms of Use and Privacy Statement
 
 
 
 Carefully read these Terms of Use before using this website. Your access to and use of this website and application for a job at 3M are conditioned on your acceptance and compliance with these terms.
 
 
 Please access the linked document by clicking here, select the country where you are applying for employment, and review. Before submitting your application, you will be asked to confirm your agreement with the terms.
</div>

Manufacturing Process Engineer

Electrolux Group

<div>
 
 Objectives of this role
 
 
 
 <ul>
 <li>
 Developing, optimizing and improving manufacturing processes to enhance productivity, quality and safety.
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 Identifying and implementing process improvements to reduce costs, minimize waste and increase efficiency.
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 Collaborating with cross-functional teams to ensure smooth integration of new processes, technologies and equipment.
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 Monitoring and analyzing process data, identifying trends and proposing solutions for process improvement continuously.
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 Performing process capability studies, statistical analysis and data-driven decision-making to achieve operational excellence and meet production targets.
 </li>
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 Ensuring compliance with safety, environmental and regulatory requirements in all process engineering activities.
 
 
 </li>
 </ul>
 
 Your tasks
 
 
 
 <ul>
 <li>
 Conduct detailed analysis and evaluation of existing manufacturing processes, identifying areas for improvement and recommending appropriate solutions.
 </li>
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 Design and implement process optimization strategies to enhance efficiency, reduce cycle time and improve product quality.
 </li>
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 Collaborate with engineering, production and quality assurance teams to develop and implement standard operating procedures (SOPs) and work instructions.
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 Monitor and analyze process performance metrics, such as cycle time, yield and scrap rate and develop strategies to meet or exceed targets.
 </li>
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 Identify and implement process control measures, including statistical process control (SPC) techniques, to ensure consistent quality and reduce process variation.
 </li>
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 Provide technical support and troubleshooting expertise to resolve process-related issues and improve overall equipment effectiveness (OEE).
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 Lead process validation activities, including protocol development, execution and documentation, ensuring compliance with regulatory requirements.
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 Participate in cross-functional teams to drive root cause analysis, corrective actions and preventive measures.
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 Provide training and guidance to production teams on new processes, procedures and equipment to ensure successful implementation and operation.
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 Stay up-to-date with the latest advancements in process engineering technologies, methodologies and best practices.
 
 
 </li>
 </ul>
 
 Required Skills And Qualifications
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in Engineering (chemical, mechanical, industrial or similar).
 </li>
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 3+ years of experience as a process engineer in a manufacturing environment.
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 Strong knowledge of process optimization techniques, lean manufacturing principles, Six Sigma methodologies and statistical analysis.
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 Proficient in process analysis, process modelling, statistical analysis and simulation software.
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 Excellent problem-solving and analytical skills with the ability to identify and resolve complex process issues.
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 Working knowledge of process safety, risk assessment and compliance with regulatory standards.
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 Effective communication and interpersonal skills to collaborate with cross-functional teams and stakeholders.
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 Ability to manage multiple projects simultaneously and meet deadlines in a fast-paced environment.
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 Strong project management skills with the ability to prioritize tasks and meet deadlines.
 
 
 </li>
 </ul>
 
 Preferred Skills And Qualifications
 
 
 
 <ul>
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 Experience with process improvement tools and methodologies such as Kaizen, 5S and Value Stream Mapping.
 </li>
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 Master&rsquo;s degree in process engineering or a related field.
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 Professional certification in process engineering or related areas.
 </li>
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 Experience with process automation and control systems.
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 Knowledge of automation and control systems, such as SCADA and PLC.
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 Knowledge of process simulation software and computer-aided design (CAD) tools.
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 Solid understanding of quality management systems, such as ISO standards.
 </li>
 </ul>
</div>

Envista Holdings

<div>Operating Company: Ormco 
Location: Sturtevant,WI,US 
Date Posted: November 10, 2025 
Req Number: R5024521</div><div></div>
 <div>Job Description: We&rsquo;re seeking a hands-on Manufacturing Process Engineer to improve and support our production operations through process optimization, data-driven problem solving, and implementation of lean manufacturing practices. This hybrid role combines process engineering&rsquo;s analytical rigor with the practical focus of manufacturing support. The role will be full time on-site. Responsibilities:<ul> <li>Analyze and improve manufacturing processes for safety, quality, and efficiency.</li> <li>Develop and implement process improvements to reduce cycle time, scrap, and downtime.</li> <li>Support daily production operations with root cause analysis and corrective actions.</li> <li>Design or modify process layouts, tooling, and fixtures to enhance manufacturability.</li> <li>Develop and maintain process documentation (work instructions, control plans, PFMEAs).</li> <li>Lead continuous improvement projects using Lean/Six Sigma methodologies.</li> <li>Train production teams and implementation of new automated processes effectively.</li> <li>Collaborate with design engineering to ensure products are optimized for manufacturability (DFM).</li> <li>Maintain and revises Engineering Document (ECR), generate (SOP), Manufacturing Control Instructions (MCI)</li> <li>Perform investigation on Material Review Disposition Record (MRDR) and apply countermeasure to eliminate root cause for failed parts</li> <li>Participate in new equipment specification, installation, and validation.</li> <li>Able to lead projects from start to finish and works well cross-functional teams.</li> <li>Responsible for finding the root cause to problems and creating then implementing a solution.</li> <li>Develop product cost estimates, and project cost, equipment cost and timeline estimates.</li> <li>Provide technical input for capital appropriation requests.</li> <li>Follows quality and safety protocols and maintains a clean working environment.</li> <li>Perform other duties and responsibilities assigned by Manager.</li></ul> Job Requirements: Minimum Qualifications:<ul> <li>Bachelor&rsquo;s degree in Mechanical, Manufacturing, or Industrial Engineering.</li> <li>2&ndash;7 years of experience in a process, manufacturing, or production engineering role.</li> <li>Proven ability to analyze data and drive measurable process improvements.</li> <li>Working knowledge of Lean principles, SPC, and root cause tools (5 Whys, Fishbone, etc.).</li></ul> Preferred:<ul> <li>CAD proficiency is a plus</li> <li>ERP or manufacturing engineering systems are a plus.</li> <li>Six Sigma Green Belt or equivalent.</li> <li>Experience with automation or process control.</li> <li>Background in continuous improvement in high-volume or precision manufacturing.</li> <li>Experience working with 3D printing</li> <li>Experience working in medical device or FDA regulated industries</li></ul> Abilities:<ul> <li>Strong communication and cross-functional teamwork skills.</li> <li>Must possess excellent communication (Technical, Oral, Written) and the ability to describe complex technical issues clearly.</li> <li>Sound understanding of regulatory and compliance documentation processes, review cycles and information repositories (meeting minutes, templates, charter documentation etc).</li> <li>Strong interpersonal skills that create followership and motivate team members.</li> <li>Driven and motivated individual with demonstrated critical thinking and analytical skills.</li> <li>Unquestionably high ethical standards and attention to reputational and compliance risks.</li> <li>Organized thinker that can prioritize tasks in real time and exercise judgment in high-paced environment.</li> <li>Plan, conduct, lead, and report on assigned projects. Review progress, evaluate results, and inform company management on assigned project status.</li> <li>Ability to travel at least 5% of the time to various manufacturing sites to oversee process implementation and provide on-site support</li></ul> Physical Demands:<ul> <li>Working hours and shifts will vary and are dependent upon the work cycles required by business needs.</li> <li>The noise level in the work environment is usually low to moderate.</li> <li>Due to the nature of product contents, careful handling and compliance to procedure and processes are required.</li> <li>Ability to stand and/or sit for long periods of time as required by business needs.</li> <li>Occasionally push, pull, lift and/or bend as required by business needs.</li> <li>Must be able to lift 25 pounds.</li></ul> #LI-RJ1 IND123 Target Market Salary Range: Actual compensation packages take into account a wide range of factors that are unique to each candidate, including but not limited to geographic location; skill sets; relevant education and certifications; depth of experience; performance; and other business and organizational needs. The disclosed reasonable estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Envista, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. The total compensation package for this position may also include an annual performance bonus, medical/dental/vision benefits, 401K match, and/or other applicable compensation plans. $94,900 &ndash; $141,900 Operating Company: Ormco Ormco is a global leader and innovator of high-quality orthodontic products and solutions, including brackets and wires. For more than 60 years, our team has partnered with the orthodontic community to help create over 20 million smiles in more than 140 countries. We build trusted relationships. Each one is rooted in respect and understanding. We take that approach when we help orthodontists achieve their clinical and practice management objectives. We take the same approach when we help our team bring their personal best to work each day, ready to make a difference and reach their full potential. Envista and all Envista Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The &ldquo;EEO is the Law&rdquo; poster is available at: http://www.dol.gov/ofccp/regs/ compliance/posters/pdf/eeopost.pdf. Envista and its family of companies (Envista) will not accept unsolicited resumes from any source other than directly from a candidate. Envista will consider unsolicited referrals and/or resumes submitted by vendors such as search firms, staffing agencies, professional recruiters, fee-based referral services and recruiting agencies (Agency) to have been referred by the Agency free of charge and Envista will not pay a fee for any placement resulting from the receipt such unsolicited resumes. An Agency must obtain advance written approval from Envista's internal Talent Acquisition or Human Resources team to submit resumes, and then only in conjunction with a valid fully-executed contract approved by the Global Talent Acquisition leader and in response to a specific job opening. Envista will not pay a fee to any Agency that does not have such agreement and written approval in place.</div>

Midea Group

<div>
 
 
 Job Responsibilities:
 
 
 
 Participate in the implementation and on-site follow-up of manufacturing process technologies during product production, including but not limited to one or more of the following tasks:
 
 
 1. Responsible for manufacturing-end technology implementation during new product development. Participate in new product development projects, assist in process route design and fixture design under mentor guidance, and track and manage product trial production, pilot production/mass production issues with closed-loop management.
 
 
 2. Develop and implement solutions for process technology issues; participate in product optimization and manufacturability enhancements during manufacturing.
 
 
 3. Manage on-site production line processes, coordinate resolution of daily process quality issues, track progress, implement corrective actions, and provide timely feedback on process information.
 
 
 4. Prepare, implement, and monitor production line process documentation; promptly address finished product feedback, ensuring timely and accurate technical modifications.
 
 
 
 
 
 
 Qualifications
 
 
 
 1. Bachelor's degree or higher; fluent English proficiency.
 
 
 2. Degree in Science, Engineering, or related fields.
 
 
 3. Proficiency in office software and design/development tools.
 
 
 Preferred Qualifications:
 
 
 1. Project management mindset and experience.
 
 
 2. Detail-oriented, diligent work ethic; preference for candidates with professional competition awards.
 
 
 Additionally, we seek candidates capable of handling high-pressure environments, possessing creative thinking, strong communication skills, and a collaborative spirit.
 
</div>

GE HealthCare

<div>
 
 Job Description Summary
 
 
 
 Engineering associated with the manufacturing process. Accountable for the quality of own work. Subject to direct operations supervision/prescribed work instructions/systems checking. Executes within a well-defined operations framework. There is generally a step by step sequence of standard operational tasks which need to be followed to achieve an end result.
 
 
 GE HealthCare is a leading global medical technology and digital solutions innovator. Our purpose is to create a world where healthcare has no limits. Unlock your ambition, turn ideas into world-changing realities, and join an organization where every voice makes a difference, and every difference builds a healthier world.
 
 
 
 Job Description
 
 
 
 
 Roles and Responsibilities
 
 
 
 <ul>
 <li>
 Manufacturing engineering tasks that do not require 4 year degree. Primarily tactical responsibilities. This does not include general administrative work.
 </li>
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 Developing conceptual knowledge of professional discipline. May include support roles with specialized expertise or technical knowledge in broad area.
 </li>
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 Applies general knowledge of business developed through education or past experience. Understands how work of own team contributes to the area.
 </li>
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 Resolves issues using established procedures. Consults supervisor or more senior team members for issues outside of defined instructions/parameters.
 </li>
 <li>
 Collaborates with others to solve issues. For customer facing roles, develops strong customer relationships and serves as the interface between customer and GE. Exchanges technical information, asks questions and checks for understanding.
 
 
 </li>
 </ul>
 
 Required Qualifications
 
 
 
 <ul>
 <li>
 Bachelors degree in Electronics/Mechanical Engineering
 </li>
 <li>
 2+ years of experience in Manufacturing process engineering
 </li>
 <li>
 Provide design &amp; assembly feedback to engineering team
 </li>
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 Experience using ERP systems - Oracle or SAP
 </li>
 <li>
 Design change and implementation experience
 
 
 </li>
 </ul>
 
 Desired Characteristics
 
 
 
 <ul>
 <li>
 Experience in Six Sigma and CAPA process
 </li>
 <li>
 Should have skills like methodical, responsive, and highly organized; have good analytical skills..
 </li>
 <li>
 Excellent knowledge of materials, parts, product design and quality standards (ISO 13485) and requirements.
 </li>
 <li>
 Good knowledge of the company&rsquo;s technology, production capabilities, tools and assembly methods and be able to use CAD (Computer aided design) tools.
 </li>
 <li>
 Good at working within budget and meeting deadlines; and have an excellent understanding of health and safety issues and requirements.
 </li>
 <li>
 Leadership skills can be an asset if their work entails overseeing and coordination of technicians
 
 
 </li>
 </ul>
 
 Inclusion and Diversity
 
 
 
 GE HealthCare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.
 
 
 We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership &ndash; always with unyielding integrity.
 
 
 Our
 
 total rewards
 
 are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you&rsquo;d expect from an organization with global strength and scale, and you&rsquo;ll be surrounded by career opportunities in a culture that fosters care, collaboration and support.
 
 
 
 
 
 Additional Information
 
 
 
 
 
 
 Relocation Assistance Provided:
 
 Yes
 
 
</div>

RBP Chemical Technology

Requirements:<ul><li>Bachelor&rsquo;s degree in Engineering (Mechanical, Chemical, Industrial, or related field)</li><li>1&ndash;2 years of hands-on experience in a manufacturing environment required</li><li>Strong problem-solving and process improvement skills</li><li>Excellent communication and team collaboration abilities</li></ul>Additional Information:<ul><li>This is an early-career opportunity; ideal for candidates with foundational engineering and manufacturing experience looking to grow.</li><li>At this time, we are unable to offer visa sponsorship. Applicants must be authorized to work in the United States without current or future sponsorship.</li></ul>General Summary:This role involves developing, evaluating, and improving manufacturing processes for increased safety, to raise efficiency, reduce cost, and improve product quality. The ideal candidate will have a strong background in engineering principles, a strong eye for detail, and the ability to work cross-functionally with other teams. Performs routine functions in a chemical laboratory, manufacturing, and office setting, assists technical personnel (Quality Control, Research and Development, and Production).Principal Duties and Responsibilities:1. Process Design and Implementation: Design and implement manufacturing processes, systems, and equipment by applying engineering principles and analysis. Develop process flow diagrams, layout plans, and capacity projections.2. Continuous Improvement: Identify and implement continuous improvement opportunities to enhance production efficiency, capacity, and quality.3. Quality Assurance: Collaborate with the quality assurance team to define quality requirements for manufacturing processes. Develop and implement process control techniques and procedures.4. Troubleshooting: Analyze manufacturing process flows for the enhancements of quality, cost reduction, and throughput. Diagnose and troubleshoot process issues and implement corrective and preventive actions.5. Project Management: Lead and manage projects related to process development and improvement, equipment installation, and start-up. Ensure projects are completed on time and within budget.6. Documentation: Prepare and maintain detailed documentation, including process maps, standard operating procedures (SOPs), and process improvement reports.7. Cross-functional Collaboration: Work closely with R&amp;D, production, maintenance, and other departments to facilitate process improvements and resolve process-related issues.8. Training: Develop and provide training for production staff on new processes, technologies, and equipment to ensure smooth implementation and operation.9. Safety and Environmental Assurance: Evaluates processes, equipment and procedures to ensure compliance with all environmental and safety rules and regulations.10. Perform Other Duties as Assigned: Conducts basic testing in different chemical products, generates, posts, and sends Certificate of Analysis, assists R&amp;D with routine basic quality and analytical testing, and supports activities in manufacturing (small batches), when required.Knowledge &amp; Background Requirements:Education Required: Bachelor&rsquo;s degree in Chemical Engineering preferred; however, will consider degrees in Industrial Engineering and Mechanical Engineering with0 - 2 years professional experience preferred.Ability to solve practical problems. Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.Ability to conduct rigorous data analysis, and the application of statistical methods to understand process variations and optimize performance. Ability to perform complex math functions, compute ratios, rates and percentages.Ability to effectively communicate with other team members.Familiarity with Microsoft Office including Outlook, Word, Excel, PowerPoint and Access.Physical Requirements: Frequently required to stand; use hands to finger, handle, or feel; reach with hands and arms; and talk or hear. Expected to react to odors, typically present in a chemical laboratory. Must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, color vision, and ability to adjust focus.Work Environment: Laboratory, office, and manufacturing environment.The above is intended to describe the general content of and requirements for the performance of this job. It is not to be construed as an exhaustive statement of duties, responsibilities or requirements.Job Type: Full-timePay: $65,000.00 - $75,000.00 per yearBenefits:<ul><li>401(k)</li><li>Dental insurance</li><li>Health insurance</li><li>Health savings account</li><li>Paid time off</li><li>Vision insurance</li></ul>Work Location: In person

Manufacturing Process Engineer – Early Career

<div><h1 class="jobSectionHeader">Job Description Summary</h1>
A dynamic engineering leader within the Process Engineering and Product Quality team, driving the development of high precision manufacturing processes for medical equipment. Lead cross functional problem-solving initiatives while ensuring strict adherence to Quality Management System (QMS) standards and regulatory compliance. 
 
GE HealthCare is a leading global medical technology and digital solutions innovator. Our purpose is to create a world where healthcare has no limits. Unlock your ambition, turn ideas into world-changing realities, and join an organization where every voice makes a difference, and every difference builds a healthier world.<h1 class="jobSectionHeader">
Job Description</h1>
Roles and Responsibilities<ul><li>
Own and lead New Product Introductions (NPIs) and manufacturing transfers for existing products by collaborating with global and local cross-functional teams including Engineering, Manufacturing, and Supply Chain teams.</li><li>
Design and develop assembly and testing processes, including jigs, fixtures, and manufacturing aids to support efficient production.</li><li>
Set up, qualify and validate assembly line tools and testing equipment to ensure robust and compliant manufacturing operations.</li><li>
Lead process risk assessments, drive factory, forward production, field quality improvements, and Defects Per Unit (DPU) reduction programs, through structured problem solving and failure analysis.</li><li>
Manage Engineering change requests and implement the change in manufacturing floor.</li><li>
Drive lean manufacturing, digitization, and plant modernization initiatives to enhance operational efficiency and productivity</li><li>
Own implementation and execution of Quality Management Systems (QMS) as per medical device regulations in shop floor. Lead QMS audits, investigations, implement CAPA.</li><li>
Coach and mentor the Process Engineering team members on process development, risk analysis, QMS and build organizational capability.</li></ul>
Required Qualifications<ul><li>
Bachelor&rsquo;s or master&rsquo;s degree in Mechanical /Production/Electrical &amp; Electronics Engineering / Bio Medical / Medical Electronics/Mechatronics Engineering.</li><li>
Knowledge/experience in Medical Equipment&rsquo;s (CT/PET)</li><li>
Sound knowledge, hands on experience on Problem Solving, failure analysis tools. (Lean, Six Sigma, data analysis).</li><li>
Knowledge of Electromechanical parts assemblies, PCB&rsquo;s.</li><li>
Knowledge of Quality Management System (QMS) for medical devices.</li><li>
Hands on experience on Microsoft office applications</li><li>
Good communication skills (Oral/Written)</li><li>
Strong bias for documentation &amp; technical reports</li><li>
Effective multitasking and ability to deliver on time and with quality.</li><li>
Ability to work in a team with good Interpersonal skills.</li></ul>
Experience<ul><li>
7 ~ 10 years in core Engineering Industry.</li><li>
Medical Device Industry experience is preferred.</li></ul>
Desired Characteristics<ul><li>
Lean Six Sigma knowledge or GB certification.</li><li>
Product development, cross-functional experience</li></ul>
Inclusion &amp; Diversity:
GE Healthcare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.
We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership &ndash; always with unyielding integrity.
Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you would expect from an organization with global strength and scale, and you will be surrounded by career opportunities in a culture that fosters care, collaboration, and support.
#LI-MA6<h1 class="jobSectionHeader">
Additional Information</h1><div><div><div><div><div><div><div>
Relocation Assistance Provided: Yes</div></div></div></div></div></div></div></div>

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