senior manufacturing engineer

NTT DATA

Req ID: 361213
 
NTT DATA strives to hire exceptional, innovative and passionate individuals who want to grow with us. If you want to be part of an inclusive, adaptable, and forward-thinking organization, apply now.
 
We are currently seeking a Senior Manufacturing Engineer to join our team in Florida, Florida (US-FL), United States (US).
 
Job Title: Senior Manufacturing Engineer
 
Location: Florida, USA
 
Position Summary
 
We are seeking an experienced Senior Manufacturing Engineer to lead complex process improvement initiatives, provide technical mentorship, and drive quality and operational excellence within a regulated medical device manufacturing environment. This role partners cross-functionally with RD, Quality, and Operations to transition products from concept to full-scale production while ensuring high-quality, compliant, and cost-effective manufacturing processes.
 
Key Responsibilities
 
Process Optimization Technical Leadership
 
•
 
Develop, implement, and optimize manufacturing processes including molding, laser welding, and bonding to improve efficiency, yield, and cost performance.
 •
 
Apply Lean Six Sigma methodologies and Design of Experiments (DOE) to drive continuous improvement.
 •
 
Create, update, and maintain manufacturing documentation including PFMEAs, Control Plans, SOPs, and Work Instructions in compliance with FDA and ISO 13485 requirements.
 •
 
Ensure processes are robust, scalable, and aligned with regulatory and quality standards.
 
Project Leadership Continuous Improvement
 
•
 
Lead cross-functional teams on process improvement, cost reduction, and capital equipment acquisition projects.
 •
 
Oversee equipment selection, installation, and validation activities (IQ/OQ/PQ).
 •
 
Collaborate with suppliers to establish process capability and ensure material and component quality.
 •
 
Drive operational excellence initiatives to enhance productivity and reduce manufacturing risk.
 
Mentorship Technical Guidance
 
•
 
Provide technical leadership and mentorship to junior engineers, technicians, and production staff.
 •
 
Support RD through Design for Manufacturability (DFM) reviews and early-stage process development.
 •
 
Develop and deliver training on new equipment, tools, and manufacturing procedures.
 •
 
Foster a culture of accountability, innovation, and continuous learning.
 
Quality Compliance
 
•
 
Lead root cause analysis (RCA) investigations for production and quality issues using structured problem-solving tools.
 •
 
Drive CAPA initiatives and ensure timely, effective resolution of non-conformances.
 •
 
Maintain strict adherence to FDA regulations, ISO 13485 standards, and internal quality systems.
 •
 
Support internal and external audits as required.
 
Qualifications
 
Education
 
•
 
Bachelor’s degree in Mechanical, Manufacturing, Biomedical, or related Engineering discipline.
 •
 
Advanced degree preferred.
 
Experience
 
•
 
Minimum of 10+ years of experience in medical device manufacturing.
 •
 
Demonstrated experience in regulated environments (FDA, ISO 13485).
 
Technical Skills
 
•
 
5+ years of proficiency in CAD software (Creo and/or SolidWorks).
 •
 
Strong statistical analysis skills with Minitab or similar tools.
 •
 
Working knowledge of Lean Six Sigma principles (certification preferred).
 •
 
3 to 5 years of experience with process validation (IQ/OQ/PQ) and DOE methodologies.
 •
 
3 to 5 years of hands-on experience with molding, laser welding, bonding, or similar precision manufacturing processes.
 
About NTT DATA
 
NTT DATA is a $30 billion business and technology services leader, serving 75% of the Fortune Global 100. We are committed to accelerating client success and positively impacting society through responsible innovation. We are one of the world's leading AI and digital infrastructure providers, with unmatched capabilities in enterprise-scale AI, cloud, security, connectivity, data centers and application services. our consulting and Industry solutions help organizations and society move confidently and sustainably into the digital future. As a Global Top Employer, we have experts in more than 50 countries. We also offer clients access to a robust ecosystem of innovation centers as well as established and start-up partners. NTT DATA is a part of NTT Group, which invests over $3 billion each year in RD.
 
Whenever possible, we hire locally to NTT DATA offices or client sites. This ensures we can provide timely and effective support tailored to each client’s needs. While many positions offer remote or hybrid work options, these arrangements are subject to change based on client requirements. For employees near an NTT DATA office or client site, in-office attendance may be required for meetings or events, depending on business needs. At NTT DATA, we are committed to staying flexible and meeting the evolving needs of both our clients and employees. NTT DATA recruiters will never ask for payment or banking information and will only use @nttdata.com and @talent.nttdataservices.com email addresses. If you are requested to provide payment or disclose banking information, please submit a contact us form, https://us.nttdata.com/en/contact-us.
 
NTT DATA endeavors to make https://us.nttdata.com accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact us at https://us.nttdata.com/en/contact-us. This contact information is for accommodation requests only and cannot be used to inquire about the status of applications. NTT DATA is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. For our EEO Policy Statement, please click here. If you'd like more information on your EEO rights under the law, please click here. For Pay Transparency information, please click here.

Senior Manufacturing Engineer

Chemlink LLC

Are you ready to take your career to the next level? At CHEMLINK LLC, we are passionate about innovation in chemical manufacturing, and we&rsquo;re looking for a Senior Manufacturing Engineer who shares our drive for excellence. This is more than a job &mdash; it&rsquo;s an opportunity to make a real impact, lead projects, and grow with a company that values your expertise.About CHEMLINK LLC:CHEMLINK LLC is a leading chemical solutions provider based in Dubai, serving industries across the UAE and beyond. We are committed to sustainable manufacturing, continuous improvement, and delivering high-quality products to our clients. Our team thrives on collaboration, creativity, and the pursuit of excellence.What You&rsquo;ll Do:Lead the design, development, and optimization of manufacturing processes, ensuring efficiency, safety, and quality.Collaborate with R&amp;D, Production, and Quality teams to scale up new products from concept to full-scale production.Identify and implement continuous improvement initiatives using Lean, Six Sigma, or other methodologies.Troubleshoot production challenges and implement practical, data-driven solutions.Mentor and guide junior engineers, fostering a culture of learning and innovation.Ensure compliance with all health, safety, and environmental regulations.Participate in strategic planning to improve plant operations, reduce costs, and increase throughput.Who You Are:Bachelor&rsquo;s degree in Chemical, Mechanical, or Industrial Engineering; a Master&rsquo;s is a plus.5&ndash;7 years of experience in manufacturing or process engineering, preferably in chemical, petrochemical, or related industries.Hands-on experience with process optimization, equipment design, and quality control.Skilled in Lean Manufacturing, Six Sigma, or other continuous improvement methodologies.Excellent problem-solving, leadership, and communication skills.Comfortable working in a multicultural and collaborative team environment.Ambitious, proactive, and eager to make a difference.What We Offer:Competitive salary and benefits package, including health insurance and annual leave.Opportunity to lead high-impact projects and advance your career.A collaborative and innovative work environment where your ideas are valued.Continuous learning opportunities, including workshops, training, and certifications.Exposure to cutting-edge chemical manufacturing technologies and processes.Work in one of the most dynamic business hubs in the world &mdash; Dubai!Pay: AED17,776.00 - AED19,875.00 per monthWork Location: In person

Modine Manufacturing Company

<div>For more than 100 years, Modine has solved the toughest thermal management challenges for mission-critical applications. Our purpose of Engineering a Cleaner, Healthier World&trade; means we are always evolving our portfolio of technologies to provide the latest heating, cooling, and ventilation solutions. Through the hard work of more than 11,000 employees worldwide, our Climate Solutions and Performance Technologies segments advance our purpose with systems that improve air quality, reduce energy and water consumption, lower harmful emissions, enable cleaner running vehicles, and use environmentally friendly refrigerants. Modine is a global company headquartered in Racine, Wisconsin (U.S.), with operations in North America, South America, Europe, and Asia. For more information about Modine, visit modine.com.<div><div><div><h2 class="jobSectionHeader">
Position Description</h2></div><div>
The Senior Manufacturing Engineer plays a critical role in driving manufacturing excellence by developing, improving, and optimizing production processes. This position focuses on technical leadership, problem-solving, and continuous improvement initiatives to enhance safety, quality, efficiency, and cost-effectiveness. The ideal candidate will have a strong background in manufacturing engineering and a passion for operational excellence, but will not have direct reports.</div></div><div><div><h2 class="jobSectionHeader">
Key Responsibilities</h2></div><div><ul><li>
Lead and support process improvement initiatives using Lean, Six Sigma, and other methodologies.</li><li>
Design, develop, and implement manufacturing processes, equipment, and tooling to improve production efficiency and product quality.</li><li>
Collaborate with cross-functional teams including production, quality, maintenance, and design engineering to resolve manufacturing issues.</li><li>
Analyze production data and metrics to identify trends and areas for improvement.</li><li>
Support new product introductions by developing and validating manufacturing processes.</li><li>
Create and maintain process documentation including work instructions, PFMEAs, and control plans.</li><li>
Ensure compliance with safety, environmental, and regulatory standards.</li><li>
Provide technical support and training to production staff as needed.</li><li>
Participate in capital equipment selection and justification.</li><li>
Drive root cause analysis and corrective actions for process-related issues.</li><li>
Other job duties as assigned.</li></ul></div></div><div><div><h2 class="jobSectionHeader">
Required Education &amp; Qualifications</h2></div><div><ul><li>
10+ years of experience in a manufacturing engineering role.</li><li>
Proven experience with Lean Manufacturing, Six Sigma, or other continuous improvement methodologies.</li><li>
Strong analytical and problem-solving skills.</li><li>
Proficiency in CAD software and manufacturing tools.</li><li>
Excellent communication and collaboration skills.</li><li>
Ability to manage multiple projects and priorities in a fast-paced environment.</li><li>
Familiarity with ERP systems and manufacturing data analysis tools.</li><li><div>
Demonstrated mechanical aptitude with the ability to understand, troubleshoot, and work with mechanical systems, tools, and equipment.</div></li></ul>
Education Requirements:<ul><li>
Bachelor&rsquo;s degree in Mechanical Engineering, Industrial, Manufacturing Engineering or a related field.</li></ul></div></div></div>
Why Choose Modine?<div> 
Health &amp; Well-being: 
Day One 
<ul><li>Competitive health, dental &amp; vision insurance coverage</li><li>Employee Assistance Program</li></ul>
After 90 days of continuous employment 
<ul><li>Maternity Leave (12 weeks at 100% pay)</li><li>8 weeks of short term disability leave paid at 100%</li><li>4 weeks of paid parental leave paid at 100%</li><li>Paternity Leave (4 weeks at 100% pay)</li></ul></div><div> 
Financial Benefits: 
<ul><li>401k Retirement plan and company paid match</li><li>Life Insurance</li><li>Health Savings Account (HSA) with employer contribution</li><li>Flexible Spending Accounts (FSA)</li><li>Short Term Disability (company paid)</li><li>Long Term Disability</li></ul></div><div> 
Work-Life Balance: 
<ul><li>Competitive time-off policies</li><li>Tuition Reimbursement</li></ul></div> 
Modine is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other characteristic protected by law. Modine provides a competitive benefit package, which could include paid vacation, short term disability, 401(k), health, dental, vision, life insurance, flex spending benefits, tuition reimbursement, Health Savings Account and much more. Human Resources will provide more detail upon your hiring. 
#LI-KM3 
#LI-Onsite</div>

Crown Equipment

<div>Company Description: 
Crown Equipment Corporation is a leading innovator in world-class forklift and material handling equipment and technology. As one of the world&rsquo;s largest lift truck manufacturers, we are committed to providing the customer with the safest, most efficient and ergonomic lift truck possible to lower their total cost of ownership.<div><div><div><h2 class="jobSectionHeader"> 
Senior Advanced Manufacturing Engineer</h2></div><div>
Responsibilities:<ul><li>
Ensure compliance with global lithium and lead-acid battery standards across manufacturing plants and branch facilities.</li><li>
Lead end-to-end implementation of battery products, including setup, ordering, delivery, storage, installation, shipping, and invoicing.</li><li>
Research and interpret country, state, and local regulations to support lithium battery deployment in new facilities.</li><li>
Collaborate with engineering and manufacturing teams to integrate lithium battery requirements into facility planning for new product introductions.</li><li>
Support Purchasing in evaluating battery suppliers, focusing on manufacturing capabilities and adherence to safety and quality standards.</li></ul>
Qualifications: 
<ul><li>8-15 years of related experience</li><li>
Bachelor&rsquo;s degree<ul><li>
 Non-degree considered if 12+ years of related experience along with a high school diploma or GED</li></ul></li><li>
Valid driving privileges</li><li>
Ability to travel frequently (6&ndash;20%), including overnight stays.</li></ul> 
Preferred Qualifications: 
<ul><li>Graduate technical degree or a combination of technical and business degrees.</li><li>
Extensive manufacturing experience, including global plant operations.</li><li>
Proven project management skills with experience leading complex, multi-year projects.</li><li>
Strong communication, interpersonal, and organizational skills.</li><li>
Knowledge of lithium battery manufacturing processes and related regulations.</li><li>
Willingness and ability to travel internationally.</li></ul></div></div></div> 
Work Authorization: 
Crown will only employ those who are legally authorized to work in the United States. This is not a position for which sponsorship will be provided. Individuals with temporary visas or who need sponsorship for work authorization now or in the future, are not eligible for hire. 
No agency calls please. 
Compensation and Benefits: 
Crown offers an excellent wage and benefits package for full-time employees including Health/Dental/Vision/Prescription Drug Plan, Flexible Benefits Plan, 401K Retirement Savings Plan, Life and Disability Benefits, Paid Parental Leave, Paid Holidays, Paid Vacation, Tuition Reimbursement, and much more.
EOE Veterans/Disabilities</div>

Senior Advanced Manufacturing Engineer - Batteries (Advanced Manufacturing Engineering)

Penspen

<div><div>Senior Instrument Engineer

Penspen www.penspen.com are looking for a Senior Instrument Engineer.

The primary location is Woking, Surrey, United Kingdom, you may be required to travel &amp; work in Al Khafji, KSA.

The Senior Instrument Engineer may operate within the Core Engineering Team or PMT project team environment. The Senior Instrument Engineer may have engineer grade instrument personnel under his responsibility and will be tasked with their control and management and the delegation of activities to such support personnel. The Senior Instrument Engineer may work under the supervision of a Lead Instrument Engineer in which case his responsibilities will be as delegated. The Senior Instrument Engineer may be in charge of any or all of the following tasks.

Knowledge / Experience (Skills):
<ul><li>At least 12 years of experience; 6 years of them within the field of Instrumentation &amp; Control Engineering for major Oil and Gas/Petrochemical projects.</li><li>PMC experience at similar role for at least several years is preferable.</li><li>Knowledge of Saudi Aramco Desktop Standard and procedures/practices is beneficial.</li><li>Previous exposure to construction and commissioning phases is beneficial but not mandatory.</li><li>Computer literate with all MS Packages, particularly Word and Excel proficient.</li><li>Experience both in Instrumentation &amp; Telecommunication.</li></ul><div> 
Qualifications: 
<ul><li>Bachelor&rsquo;s Degree in Instrumentation &amp; Control Engineering/Electrical/Electronic or Mechanical Engineering</li></ul></div> 


If you have the skills, please apply by clicking this link - https://careers.penspen.com/vacancy/senior-instrument-engineer-608188.html#hs_show_apply_popup=true

#LI- AS2

#LI-ONSITE</div></div>

Senior Instrument Engineer

Mosaic People Solutions on Behalf of Client

The Senior Engineer, Catheter NPI &amp; Manufacturing is responsible for leading the transfer, scale-up, and commercialization of catheter-based medical devices to contract manufacturers (CMOs) for Arga Medtech Inc. This role ensures successful externalization of manufacturing through robust design transfer, process validation, and supplier integration. Develops technical solutions to complex manufacturing challenges and works cross-functionally to ensure CMOs are fully capable, qualified, and scalable for commercial production.ESSENTIAL DUTIES AND RESPONSIBILITIES:Design Transfer &amp; CMO Externalization<ul><li>Lead end-to-end transfer of catheter products from R&amp;D to established contract manufacturers, including planning, execution, and post-transfer stabilization.</li><li>Develop and own comprehensive technology transfer packages (process flows, BOMs, work instructions, equipment specifications, test methods, and training materials).</li><li>Ensure full alignment between DHF and DMR, with clear translation of design outputs into manufacturable specifications at the CMO.</li><li>Define transfer strategy including build plan (alpha, pilot, validation, ramp) and success criteria.</li><li>Establish manufacturing equivalency between internal development builds and CMO production.</li></ul>Manufacturing Fixture &amp; Tooling Development<ul><li>Design, develop, and qualify custom manufacturing fixtures and tooling to support catheter assembly processes (e.g., bonding, alignment, tipping, reflow).</li><li>Translate process requirements into fixture design specifications, including tolerance stack-ups, alignment constraints, thermal considerations, and operator interaction.</li><li>Develop rapid prototype fixtures (e.g., 3D printed, machined) to support engineering builds and process development.</li><li>Collaborate with internal teams and/or CMOs to transition prototype fixtures into production-ready tooling.</li><li>Generate and maintain fixture documentation packages (drawings, BOMs, work instructions, maintenance requirements).</li><li>Ensure fixtures are scalable, repeatable, and suitable for transfer to manufacturing environments.</li></ul>CMO Readiness &amp; Qualification Execution<ul><li>Partner with Supply Chain and Quality to support CMO onboarding and qualification activities.</li><li>Execute technical capability assessments and gap closure plans for assigned CMOs.</li><li>Define equipment, tooling, and infrastructure requirements to enable successful transfer.</li><li>Support first article inspection (FAI) and process qualification readiness.</li><li>Ensure CMO alignment with FDA QSR, ISO 13485, and internal quality requirements.</li></ul>Process Development, Industrialization &amp; Validation<ul><li>Transfer and scale catheter manufacturing processes (e.g., bonding, shaft assembly, tipping, coating, extrusion interfaces) to CMO environments.</li></ul>&middot; Author and execute protocols and reports for design verification &amp; design validation activities. This includes shelf-life packaging testing, product functionality and performance testing.<ul><li>Author and execute process validation (IQ/OQ/PQ) at the CMO, including protocol development, execution oversight, and report approval.</li><li>Develop and industrialize catheter manufacturing processes, including design and integration of fixtures and tooling required to ensure repeatability and scalability.</li><li>Incorporate fixtures into process validation activities (IQ/OQ/PQ), ensuring they are qualified and capable of consistently meeting process requirements.</li><li>Define and monitor critical process parameters (CPPs) and critical quality attributes (CQAs).</li><li>Ensure appropriate process controls, in-line inspection methods, and SPC systems are implemented at the CMO.</li><li>Drive process robustness and repeatability across sites.</li></ul>Build Execution &amp; Production Ramp<ul><li>Plan and execute engineering builds, pilot builds, and validation builds at the CMO.</li><li>Transfer fixture designs and tooling requirements to contract manufacturers, ensuring accurate replication and implementation.</li><li>Provide on-site technical support during builds, including troubleshooting and operator training.</li><li>Establish yield targets, scrap reduction plans, and ramp metrics.</li><li>Drive resolution of build issues through structured root cause analysis (DOE, 5-Why, Fishbone).</li><li>Transition ownership to sustaining teams post-launch with clear handoff criteria.</li></ul>Supplier &amp; CMO Performance Management<ul><li>Serve as primary technical interface between Arga and CMO engineering/manufacturing teams.</li><li>Establish and monitor KPIs (yield, cycle time, cost, quality) for CMO performance.</li><li>Lead continuous improvement and value engineering initiatives with CMOs.</li><li>Support and resolve NCR, CAPA, and deviation investigations related to CMO production.</li><li>Drive change management (ECO/ECN) implementation across internal and external stakeholders.</li></ul>Cross-Functional Leadership &amp; Compliance<ul><li>Partner with Quality, Regulatory, and Supply Chain to ensure compliant and efficient product transfer.</li><li>Support regulatory submissions and audits related to manufacturing transfer or process changes.</li><li>Lead risk management activities (PFMEA, control plans) specific to CMO processes.</li><li>Ensure all activities meet design control and quality system requirements.</li></ul>Documentation &amp; Systems<ul><li>Develop and maintain DMR, process documentation, work instructions, and training materials at the CMO.</li><li>Ensure traceability between design requirements, process controls, and inspection methods.</li><li>Review and approve CMO-generated documentation for alignment with product requirements.</li></ul>EXPERIENCE &amp; QUALIFICATIONS:&middot; Bachelor&rsquo;s Degree in Mechanical Engineering, Biomedical Engineering, or related field, or equivalent experience.&middot; 10+ years of experience in medical device engineering with strong emphasis on NPI, design transfer, and CMO execution.&middot; Proven track record of successful product transfer to contract manufacturers, including validation and commercial ramp.&middot; Deep expertise in catheter manufacturing processes and materials.&middot; Proven experience designing and implementing fixture-driven process solutions for catheter or complex assembly manufacturing.&middot; Strong experience with process validation (IQ/OQ/PQ), DOE, SPC, and statistical methods.&middot; Experience working with global CMOs and supplier networks.&middot; Working knowledge of CAD tools including experience with SolidWorks.&middot; Strong understanding of FDA QSR, ISO 13485, and regulatory expectations.&middot; Strong understanding of ISO 10555-1.&middot; Experience supporting regulatory submissions, audits, and inspections related to manufacturing sites.&middot; Demonstrated leadership in cross-functional and matrixed environments.&middot; Experience managing engineers or technical teams preferred.Pay: From $120,000.00 per yearBenefits:<ul><li>401(k)</li><li>Health insurance</li><li>Paid time off</li></ul>Application Question(s):<ul><li>What is your desired salary?</li><li>How many years of experience in medical device engineering with emphasis on NPI, Design transfer, and CMO execution do you have?</li><li>How many years have you worked with catheters? </li></ul>Work Location: In person

Senior Engineer, Catheter NPI & Manufacturing

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Senior Engineer, Catheter NPI & Manufacturing