Process Engineer III, Franklin Machining
Manufacturing engineer job in Bellingham, MA
Process Engineer - Medical Device Manufacturing
Location: Franklin, MA | Full-Time
About the Role
We are seeking a Process Engineer III with strong manufacturing experience to support machining operations in the medical device industry. This role involves development and improvement of machining processes, solving complex manufacturing challenges, and driving process improvements to ensure precision, compliance, and efficiency. You will play a key role in equipment selection, capacity planning, and cost analysis while collaborating across engineering, quality, and production teams.
Key Responsibilities
Develop machining processes and operation sheets from engineering data for complex medical devices.
Implement new or improved manufacturing methods, tools, and equipment designs to optimize performance.
Lead cost reduction initiatives and evaluate outside processes for quality and efficiency.
Design and implement assembly tooling, jigs, and fixtures.
Manage multiple projects, track progress, and report regularly to management.
Partner with Quality to analyze data and drive corrective actions.
Create and maintain clear, accurate documentation to support production, compliance, and knowledge transfer.
Ensure compliance with FDA, ISO 13485, ISO 9001, and GMP standards.
Train personnel and provide daily communication across departments to resolve production issues.
Qualifications
Bachelor's degree in Mechanical or Industrial Engineering.
5+ years of experience in machining, CNC equipment, and medical device assembly.
Strong knowledge of GD&T, metrology tools (CMM, profilometer, vision systems), and process monitoring.
Familiarity with GMP, ISO, Lean manufacturing; Lean Six Sigma certification a plus.
Experience with ERP systems (SAP/Oracle) and MS Office tools (Word, Excel, Project, PowerPoint).
Excellent communication skills and ability to manage multiple priorities.
Proven ability to generate thorough documentation for processes, tooling, and testing.
Why Join Us
Contribute to the development of life-changing medical technologies.
Work in a collaborative, innovation-driven environment.
Competitive compensation, benefits, and career growth opportunities.
Who we are:
KARL STORZ is an independent, family-owned company headquartered in Germany's renowned MedTech manufacturing region. For 80 years, we've pioneered the most groundbreaking innovations in endoscopic surgery, video imaging, and operating room integration to benefit patients and healthcare providers alike.
With more than 9,000 associates worldwide and 2,600 in the US, we pride ourselves on harnessing cutting-edge technology, precise workmanship, and unrivaled customer support to help healthcare facilities succeed. With onsite locations and field opportunities across the country, we attract a diverse and talented staff. It's not just about the tools we create-it's about the lives we change, together.
#LI-CW1
Smart Contract Engineer/Data Science Associate
Manufacturing engineer job in Boston, MA
The Role
We are seeking a highly skilled and technically driven individual with deep expertise in blockchain engineering and applied data science to join Fidelity Digital Asset Management. This role is ideal for a hands-on expert who thrives in architecting and deploying advanced blockchain solutions, smart contracts, and quantitative models that support Research, Trading, Risk, and Operations. You will serve as a senior technical authority, driving innovation and ensuring the robustness of our digital asset infrastructure.
Key Responsibilities
Architect and oversee the development of blockchain-based systems and smart contracts across EVM, Solana, and Cosmos SDK platforms.
Lead technical design and implementation of crypto infrastructure, including secure deployment pipelines, testing frameworks, and audit processes.
Collaborate with quant researchers and data scientists to integrate blockchain data into predictive models, optimization engines, and trading algorithms.
Conduct deep technical reviews and audits of smart contracts, ensuring security, scalability, and compliance with DeFi standards.
Evaluate and implement emerging technologies, protocols, and tooling to enhance Fidelity's digital asset capabilities.
Serve as a technical liaison across engineering, trading, and risk teams to ensure seamless integration of blockchain systems into core workflows
The Expertise and Skills You Bring
4+ years of hands-on experience in blockchain engineering, smart contract development, or crypto infrastructure, with a strong track record of technical delivery.
Deep understanding of EVM/SVM architecture, token standards (ERC-20, ERC-721, SPL), and DeFi primitives.
Proficiency in multiple programming languages including Python, Solidity, and JavaScript/TypeScript.
Experience with smart contract frameworks and tools such as Hardhat, Truffle, OpenZeppelin, Mythril, and Ganache.
Strong background in quantitative modeling, data science, or financial engineering, with experience applying models to trading or risk systems.
Proven ability to lead complex technical projects and mentor senior engineers in a collaborative, high-performance environment.
The Team
Fidelity Digital Asset Management [FDAM] is building an investment platform offering digital asset products and services designed to meet the growing needs of Fidelity's retail customers and intermediary and institutional clients. The Data Science team is a highly collaborative group leading technical projects across the FDAM organization to enable effective management of investment products and services. Project examples include integration of vendor infrastructure, constructing models or tools, building automation across technologies, and portfolio or business analytics. As a hands-on team lead you will be expected to understand the function needs to both meet the expected outcome and continue to drive innovation
The base salary range for this position is $140,000-285,000 USD per year.
Placement in the range will vary based on job responsibilities and scope, geographic location, candidate's relevant experience, and other factors.
Base salary is only part of the total compensation package. Depending on the position and eligibility requirements, the offer package may also include bonus or other variable compensation.
We offer a wide range of benefits to meet your evolving needs and help you live your best life at work and at home. These benefits include comprehensive health care coverage and emotional well-being support, market-leading retirement, generous paid time off and parental leave, charitable giving employee match program, and educational assistance including student loan repayment, tuition reimbursement, and learning resources to develop your career. Note, the application window closes when the position is filled or unposted.
Please be advised that Fidelity's business is governed by the provisions of the Securities Exchange Act of 1934, the Investment Advisers Act of 1940, the Investment Company Act of 1940, ERISA, numerous state laws governing securities, investment and retirement-related financial activities and the rules and regulations of numerous self-regulatory organizations, including FINRA, among others. Those laws and regulations may restrict Fidelity from hiring and/or associating with individuals with certain Criminal Histories.
Most roles at Fidelity are Hybrid, requiring associates to work onsite every other week (all business days, M-F) in a Fidelity office. This does not apply to Remote or fully Onsite roles.
Certifications:Category:Data Analytics and Insights
Mechanical Design Engineer
Manufacturing engineer job in Westborough, MA
Ascendion is a full-service digital engineering solutions company. We make and manage software platforms and products that power growth and deliver captivating experiences to consumers and employees. Our engineering, cloud, data, experience design, and talent solution capabilities accelerate transformation and impact for enterprise clients. Headquartered in New Jersey, our workforce of 6,000+ Ascenders delivers solutions from around the globe. Ascendion is built differently to engineer the next. Ascendion | Engineering to elevate life
We have a culture built on opportunity, inclusion, and a spirit of partnership. Come, change the world with us:
Build the coolest tech for world's leading brands.
Solve complex problems - and learn new skills.
Experience the power of transforming digital engineering for Fortune 500 clients.
Master your craft with leading training programs and hands-on experience.
Experience a community of change makers!
Join a culture of high-performing innovators with endless ideas and a passion for tech. Our culture is the fabric of our company, and it is what makes us unique and diverse. The way we share ideas, learning, experiences, successes, and joy allows everyone to be their best at Ascendion.
About the Role:
Job Title: Mechanical Design Engineer
Overview:
Scope of Work: As a Mechanical Engineer at Client, your goal will be to help with the mechanical design and systems integrations. You will need to have experience in a multidisciplinary team (Mechanical, Electrical, Software, etc.) You do not need to have expertise in other disciplines, but you should be able to communicate/understand other disciplinary requirements and how it may effect your own requirements.
Key Responsibilities:
Thorough understanding and use of principals, theories and concepts in mechanical engineering.
Strong organizational skills and the ability to work well with teams.
Ability to effectively communicate concepts and write technical documents.
Ability to create easy to understand documentation.
Proficiency with Product Lifecycle Management PLM software and ECO's (Agile).
Experience in the design of complex mechanical products and equipment.
Strong problem solving skills.
Experience in Design for Manufacturing, Design for Assembly, Design for Serviceability.
Proficiency with SolidWorks Simulation or Ansys Finite Element Analysis tools.
Minimum Qualifications:
BS in Mechanical Engineering or related discipline.
3+ years of experience working in mechanical engineering or related field.
SolidWorks or similar CAD experience with best practices for part design, advanced assemblies, complex configuration management.
Hands on experience crafting simple proof-of-concept models.
Location: Westborough MA
Salary Range: The salary for this position is between $115,000- $120,000 annually. Factors which may affect pay within this range may include geography/market, skills, education, experience, and other qualifications of the successful candidate.
Benefits: The Company offers the following benefits for this position, subject to applicable eligibility requirements: [medical insurance] [dental insurance] [vision insurance] [401(k) retirement plan] [long-term disability insurance] [short-term disability insurance] [5 personal days accrued each calendar year. The Paid time off benefits meet the paid sick and safe time laws that pertains to the City/ State] [10-15 days of paid vacation time] [6 paid holidays and 1 floating holiday per calendar year] [Ascendion Learning Management System]
Want to change the world? Let us know.
Tell us about your experiences, education, and ambitions. Bring your knowledge, unique viewpoint, and creativity to the table. Let's talk!
Principal Optical Engineer
Manufacturing engineer job in Boston, MA
The Hardware Engineering Group at my client is seeking strong candidates for a Principal Optical Engineer to serve as a senior individual contributor to the company's mission of building state-of-the-art, manufacturable, and deployable neutral atom quantum computers. The Hardware Engineering Group plays a crucial role in accelerating the company's technology leadership and translating the company's scientific breakthroughs into products delivered to customers. To accomplish this mission, we are looking to hire a candidate with graduate-level education in optics, optical engineering, or applied physics with industry experience in an enterprise engineering environment. The ideal candidate will combine a deep, fundamental understanding of several areas of optics, design, and engineering. Although candidates with a Ph.D. in physics may be considered, applicants should ensure they have sufficient professional experience beyond academia in an enterprise engineering environment to establish themselves independently as a Principal-level engineer.
Key Job Responsibilities
Optical module design and development
Work with physicists to understand requirements and architect optical systems, sub-systems, modules, and components to support my clients neutral atom computers through the full development lifecycle (R&D, productization, maintenance, and beyond).
Technically lead an interdisciplinary team of engineers (optical, electronic, mechanical, etc.) through the product development process to take an optical module from early phase concept through to implementation and production.
Advance state-of-the-art engineering practices at my client through independent research, problem-solving, and continuous improvement initiatives.
Coordinate closely with the R&D/science team to enable cutting-edge R&D and translate scientific advances into the next generation of products.
Troubleshoot technical issues at company headquarters and off-site installations at customer locations (in coordination with local support team).
Qualifications
Required:
Master's degree in optics, optical engineering, applied physics, or a closely related field.
10-15 years non-academic work experience. Experience at an enterprise scale as well as startup preferred.
Deep experience and knowledge of
Free-space optics
Lens design
Fiber optics
Lasers
Optical system characterization and testing
Opto-mechanics
Experience bringing complex optical systems from concept to production
Expertise with using Mechanical CAD software (e.g. Inventor, Solidworks), Product Data Management (PDM) software, Product Lifecycle Management (PLM) software
Expertise with Optical simulation software (e.g. Zemax)
Preferred:
Experience with quantum computing, especially neutral atom
Professional work experience in commercial product development and off-site product deployment at customer premises.
The approximate base salary range for this position is $151,200 - $236,250.
We consistently monitor external market data and update base salary ranges accordingly. We determine base compensation decisions on several factors, including as geographic placement, role-specific knowledge, skills, and/or experience. In addition to our base salary offerings, we also provide equity grants for all new hires.
Mechanical Engineer (electrical power distribution)
Manufacturing engineer job in Hingham, MA
Skills Matrix
• Bachelor's degree in Mechanical Engineering
• 2+ years of experience with the following:
• 3D Solid modeling experience related to component/system design in Creo/ProE
• Direct or related functions in design/ R&D of the mechanical aspects of electrical power distribution products.
Required:
Basic Qualifications:
Bachelor's degree in Mechanical Engineering
2+ years of experience with the following:
3D Solid modeling experience related to component/system design in Creo/ProE
Direct or related functions in design/ R&D of the mechanical aspects of electrical power distribution products.
Working independently and within a team environment
Strong problem-solving skills
Proficiency with Microsoft Office suite
Professional verbal and written communication skills in English.
Legally authorized to work in the United States on a continual and permanent basis without company sponsorship
Preferred Qualifications:
Experience with ATS (automatic transfer switches)
Responsibilities:
Developing mechanical components of electrical distribution equipment.
Testing mechanical components.
Designing, Identifying and selecting components, materials, parts, and semi-products appropriate for mechanical systems.
Creating mechanical models and tolerance analyses to simulate mechanical design concepts.
Calculating and creating final layout including documentation and specification for parts, assemblies, or finished products.
Maintaining technical product files.
Analyzing existing development procedures and suggests improvements.
Implementing or testing design solutions.
Upgrading the design of existing devices by adding mechanical elements.
Analyzing localization requirements and designing/adapting products and solutions accordingly.
Traveling to manufacturing locations and testing laboratories for new product implementation; visiting suppliers and customers.
Process Engineers
Manufacturing engineer job in Boston, MA
Nationwide Opportunities Do you thrive on optimizing systems, improving yields, and driving operational excellence? Whether your background is in pharma, biotech, medical device, or advanced manufacturing, we'd love to connect. At Scientific Search, we partner with industry leaders and emerging innovators across the U.S. who rely on talented Process Engineers to enhance production efficiency, scale technologies, and ensure consistent product quality. We're continually supporting new searches and always expanding our network of process professionals.
We're Interested In Connecting With Engineers Experienced In
Process development, scale-up, and optimization
Equipment design, installation, and validation
Root cause analysis, troubleshooting, and continuous improvement (Six Sigma, Lean)
cGMP manufacturing support within regulated environments
Cross-functional collaboration with operations, quality, and R&D teams
If you'd like to be considered for future Process Engineer roles, please send us your resume. We'll keep you in mind as new positions arise that fit your expertise, interests, and preferred locations.
Submit your resume
We're always growing our network of skilled Process Engineers - let's stay connected so we can help you discover the right opportunity when the time is right. #19580
Machine Learning Engineer
Manufacturing engineer job in Cambridge, MA
🤖 Machine Learning Engineer | Scalable Systems | Onsite (Cambridge, MA)
A rapidly growing tech startup is building AI-driven, high-performance systems designed to solve complex, real-world challenges. The team blends software engineering and systems optimization to create scalable, reliable technology that supports next-generation applications.
As an ML Engineer, you'll take models from idea to production - implementing, optimizing, and scaling them to handle massive workloads efficiently. You will be collaborating closely with other engineers to build AI systems that are reliable, maintainable, and ready for real-world deployment.
💡 What you'll do:
• Develop, deploy, and optimize ML models for production use
• Integrate & monitor AI pipelines with engineering teams
• Ensure models are efficient, scalable, & aligned with product goals
If you're excited to engineer AI systems that truly scale, this is your chance to make a meaningful impact.
📍 Office: Cambridge, MA (Onsite)
💰 Up to $300,000 (dependant on exp.) + equity options
Interested? Apply now!
Machine Learning Engineer (Computer Vision and/or Robotics) - Series A Startup
Manufacturing engineer job in Boston, MA
If you've ever wanted to apply your ML and robotics / Computer Vision skills to something that truly moves the needle, this is that role.
You'll join a fast-growing tech company building next-generation autonomous systems that can operate in environments where GPS fails and traditional AI breaks down.
Our client's mission? To push the boundaries of what's possible in autonomy, from national security to real-world commercial use cases in logistics, emergency response, and exploration. If you're driven by complex technical challenges and the idea of shaping the future of intelligent machines, read on.
What You'll Do
Design, train, and deploy ML models for advanced computer vision and robotic perception.
Build large-scale training pipelines and tune models for performance and reliability.
Integrate ML systems into real-world hardware platforms, turning research into production.
Collaborate with some of the brightest minds in AI and autonomy.
Write clean, efficient code in Python and/or C++, and stay ahead of the curve with state-of-the-art techniques.
What You Bring
A degree in Computer Science, Engineering, or similar field.
Proven hands-on experience applying ML to computer vision and/or robotics problems.
Proficiency with PyTorch or TensorFlow.
Strong coding skills in Python or C++ (ideally both).
Experience deploying ML models and building scalable training pipelines.
Familiarity with modern development tools (Git, CI/CD, etc.).
Bonus points if you've worked with:
CUDA kernel optimization, ONNX/TensorRT/OpenVINO, ROS2, SLAM, sensor fusion, or real-time inference pipelines.
Why You'll Love It Here:
Work at the bleeding edge of AI and robotics innovation.
Collaborate with engineers and researchers from leading institutions.
Directly impact real-world autonomous missions and commercial deployments.
Competitive salary, meaningful equity, and comprehensive benefits (medical, 401(k), pet insurance, and more).
If you're passionate about machine learning, robotics, and real-world impact, this is your chance to build something that truly matters.
Apply now and help define the next generation of autonomous intelligence.
ALM Process Engineer
Manufacturing engineer job in Boston, MA
The Process Engineer is responsible for analyzing, designing, and optimizing operational workflows across the organization. This role focuses heavily on documenting standard operating procedures (SOPs), building clear process maps, and driving efficiency improvements. The ideal candidate is fast, detail-oriented, and skilled at transforming complex information into simple, intuitive workflows that teams can follow.
Key Responsibilities
Develop, update, and optimize end-to-end process workflows using tools such as Lucidchart, Visio, or Miro.
Create clear, concise, and accurate Standard Operating Procedures (SOPs), work instructions, and process documentation.
Partner with operations, technology, and leadership teams to gather requirements and understand current-state processes.
Identify inefficiencies or gaps and recommend improvements to streamline operations.
Maintain a centralized library of process documentation that is easy for employees to understand and access.
Support new system implementations by documenting workflows, mapping integrations, and validating process changes.
Conduct process walkthroughs, training sessions, and knowledge-transfer workshops.
Monitor process performance and track KPIs to ensure improvements deliver measurable results.
Ensure that all processes comply with internal controls, quality standards, and organizational policies.
Qualifications
Bachelor's degree in Engineering, Operations Management, Industrial Engineering, or a related field (or equivalent experience).
2-5+ years of experience in process engineering, operations improvement, or workflow design.
Strong experience with workflow design software (Lucidchart, Visio, Miro, etc.).
Exceptional documentation skills and ability to convert complex processes into simple steps.
Strong analytical and problem-solving abilities.
Excellent communication and collaboration skills.
Ability to work quickly and accurately in a fast-paced environment.
Knowledge of Lean, Six Sigma, or continuous improvement methodologies is a plus.
Key Traits
Fast learner with an ability to quickly turn ideas into documented workflows.
Highly organized and detail-driven.
Comfortable working independently and managing multiple projects simultaneously.
Process-minded with a passion for operational excellence.
Power Plant Engineer
Manufacturing engineer job in Cambridge, MA
Job title: Senior PSA Engineer DTS
Must have skills:
Bachelor's degree in electrical engineering
1.Implement, configure, and maintain GE AEMS applications for real-time and planning environments.
2.Develop and validate DTS models within GE AEMS for dynamic stability and contingency analysis.
3. Perform transient stability, voltage stability, and dynamic simulations using GE AEMS tools.
4. Integrate renewable generation and FACTS devices into DTS models.
5. Ensure adherence to NERC, FERC, and regional reliability standards.
Detailed Job Description:
Bachelor's degree in electrical engineering
The Senior PSA Engineer DTS will lead advanced Power System Analysis PSA and Dynamic Transmission System DTS initiatives within a power utility environment. This role requires hands-on expertise in GE AEMS Advanced Energy Management System for real-time operations, stability studies, and integration of dynamic models to ensure grid reliability and compliance.
Minimum years of
experience: 8-10 years
Education: Bachelor's degree in electrical engineering
Process Engineer III
Manufacturing engineer job in Woburn, MA
Vaxess is a NIH and venture-funded company developing a pipeline of next-generation vaccines and therapeutics on the MIMIX platform. With only five minutes of wear-time on the skin, the self-applied MIMIX patch enables up to two weeks of sustained delivery. The platform combines high temperature stability with simplified application to dramatically alter the way that drugs are delivered. Vaxess is committed to enabling products that are not only more effective, but also more accessible to patients around the world.
Research & development at Vaxess is cross-disciplinary, integrating mechanical, industrial, biomedical, and
chemical engineering with chemistry, biology, and human factors to address important unmet medical needs.
We are seeking a talented, collaborative, and highly motivated engineer to join our growing team. This role offers a unique opportunity to build manufacturing capacity from the ground up to bring innovative technology to theglobal vaccine and therapeutic market.
Responsibilities
Characterize and improve manufacturing process unit operations by designing, executing, and analyzing process development experiments; communicate results via written reports and oral presentations to internal and project teams
Support manufacturing scale-up by assessing novel equipment, work flows, analytical techniques/PAT, and process configurations
Support manufacturing operations by incorporating equipment and process improvements within established processes and equipment trains, and by revising manufacturing batch records, SOPs, and other controlled documents to reflect changes; contribute to implementing and maintaining Vaxess' Quality System.
Supervise and mentor junior engineer(s) and technicians, including a direct report
Collaborate closely with cross-functional teams to support product development and manufacturing activities
Qualifications
BS in Mechanical Engineering, Biomedical Engineering, or a related discipline
5 - 7 years of relevant direct R&D experience within the medical device or biopharmaceutical industries;
experience working on combination products is highly desirable
Demonstrated success using empirical and first-principles models to inform and analyze experiments; experience with statistical methodologies and working with large data sets (e.g. Six Sigma, DoEs, multivariate techniques) is a plus
Excellent time and project management skills and proven ability to meet goals and deadlines
Demonstrated abilities to learn new skills and fields, creatively solve challenging technical problems, think independently, and work collaboratively in diverse multidisciplinary teams
Entrepreneurial spirit and drive to positively impact global human health
Vaxess is building a team of exceptional people to rapidly advance product development. We work closely as a team and thrive in a dynamic, exciting, and engaging work environment. If you're interested in joining the Vaxess team, please submit your CV/resume to ******************.
Hardware/System Sustaining Engineer
Manufacturing engineer job in Milford, MA
Job Title: Hardware/System Sustaining Engineer
Details:
Type: On-site
Duration: Permanent Direct Hire
Salary: $ Depending on Experience
The Hardware Sustaining Engineer is responsible for supporting, maintaining, and improving existing hardware products throughout their lifecycle. This role bridges design engineering, component engineering, manufacturing, and quality to ensure product reliability, manufacturability, and continued compliance with standards. The role involves diagnosing hardware/system issues, instituting design updates, and designing and implementing automated product test applications.
Key Responsibilities:
Product Support & Maintenance
Provide engineering support for released hardware products across their lifecycle.
Investigate, troubleshoot, and resolve hardware failures in production, field, and customer environments.
Develop and implement engineering change orders / product change notices (PCNs) to address design improvements, manufacturing improvements, and component obsolescence.
Support supply chain in evaluating alternate components and managing end-of-life (EOL) parts.
Manufacturing & Quality Interface
Collaborate with manufacturing teams to resolve build and test issues.
Support failure analysis, root cause identification, and corrective/preventive actions (CAPA).
Work with design engineering and quality teams to maintain compliance with applicable safety, regulatory, and industry standards.
Product Documentation
Maintain and update design documentation, schematics, BOMs, and test procedures.
Validate and verify design changes through lab testing and simulations.
Define test plans for verification of new designs.
Qualifications:
Bachelor's degree in Electrical Engineering, Computer Engineering, or related field.
3-7 years of experience in hardware design, sustaining engineering, or manufacturing support.
Strong knowledge of analog/digital electronics, PCB design, and system-level troubleshooting.
Experience with lab equipment (oscilloscopes, logic analyzers, power analyzers, etc.).
Familiarity with industry standards (UL, FCC, CE, ISO, etc.).
Strong problem-solving and root-cause analysis skills.
Excellent communication skills for cross-team collaboration and reporting.
Preferred Skills:
Experience with Python and manufacturing test scripting.
Experience conducting DVT and reliability testing.
Knowledge of supply chain and component lifecycle management.
Hands-on experience with CAD tools (e.g., Altium, OrCAD) and PLM systems.
Ability to work in fast-paced, cross-disciplinary environments.
Compliance / Export Control:
This position may include access to technology and/or software source code subject to U.S. export controls (including ITAR). Applicants will be required to provide information regarding citizenship/immigration status for compliance. The company may decline to proceed if authorization is required and cannot be obtained.
Company Overview:
Founded in 2010, Top Prospect Group was created with a focus on matching high-quality candidates with top clients while fostering an environment where success is shared by all. In 2023, the company was acquired by HW Staffing Solutions, expanding its service offerings to include technology and professional services.
Qualified candidates are encouraged to apply immediately!
Please include a clean copy of your resume, salary expectations, and any references in your application
.
POS Quality Engineer
Manufacturing engineer job in Canton, MA
Our client is seeking a POS Quality Engineer to join their team! This position is located in Canton, Massachusetts.
Execute functional testing for the client's POS systems in a lab environment
Validate new POS features, patches, upgrades, and configuration changes
Troubleshoot issues across POS hardware, networking, integrations, and payment systems
Review logs, identify root causes, and escalate defects to internal teams and vendors
Collaborate with vendors delivering POS products to ensure quality and readiness
Support daily version testing, weekly releases, and continuous enhancements
Maintain test cases, regression suites, and documentation
Ramp up on the clients POS systems, environments, and workflows
Execute manual testing independently and efficiently
Understand integration points with kiosk, mobile apps, loyalty, and payments
Build relationships with product, engineering, and vendor teams
Contribute to expanding and maintaining POS test automation frameworks
Improve test coverage, defect identification, and issue resolution speed
Work independently with minimal oversight while communicating affectively
Support performance-related testing for high-volume transaction scenarios
Help streamline testing workflows to support frequent deployments
Desired Skills/Experience:
5+ years of POS Quality Engineering experience
Hands-on experience with any POS system such as: Aloha, Toast, NCR, Oracle Symphony, or other enterprise/custom POS systems
Experience with payment systems such as: VeriFone, kiosk integrations, loyalty platforms, mobile ordering, and web integrations
Strong manual testing proficiency with the ability to execute tests quickly and accurately
Ability to troubleshoot logs, hardware, and light networking issues
Experience collaborating with third-party vendors on POS deliverables
Familiarity with automation frameworks and ability to contribute to automation improvements
Prior experience working in a POS lab environment (devices, staging stores, simulators)
Strong communication, organization, and self-management skills
Benefits:
Medical, Dental, & Vision Insurance Plans
Employee-Owned Profit Sharing (ESOP)
401K offered
The approximate pay range for this position is between $55.00 and $65.00. Please note that the pay range provided is a good faith estimate. Final compensation may vary based on factors including but not limited to background, knowledge, skills, and location. We comply with local wage minimums.
Quality Systems Engineer (Medical Devices Industry) @ Andover, MA
Manufacturing engineer job in Andover, MA
WHO WE ARE
Nextphase.ai is a Data Management solution provider focused on Data Operations services for enterprise data in the cloud. We are leading the innovation agenda with our clients by delivering a portfolio of services to help them improve data quality and manage data governance for their cloud data. NextPhase.ai data management services are tailored to achieve our client's business outcomes thus enabling our clients to focus on monetizing their data while we handle data operations. Nextphase.ai provides you with a dynamic and fun work environment and encourages you to use creative thinking to solve client challenges.
Position Overview:
We are seeking a dynamic, analytical thinking individual to join our Quality team, this is a contract position focusing on Quality Systems, CAPA, Complaint handling, Internal Audit, metric reporting and process improvement initiatives. The ideal candidate will possess a strong background in medical devices or IVD, with a proven track record in managing quality-related activities in a fast-paced dynamic environment. QMS experience is essential.
Responsibilities:
This position is responsible for, but not limited to, the following:
Supports the overall QMS processes for the organization. Responsible for activities required to ensure compliance of Quality Management Systems (QMS), specifically regarding CAPA, complaints and internal/external audits. Additional responsibilities include supporting other QMS functions such as NCMRs, Supplier Controls, Management Review, Risk Review, etc.
Execution and coordination of activities associated with CAPA program, including administration and record management, providing quality input to investigations, reporting, as well as metrics and trending
Support CAPA Owners in quality-related technical principles, including but not limited to Problem Solving tools and techniques (Root Cause Analysis, DOE, FMEA, etc.)
Investigate customer complaints, from intake through investigation and closure
Manages the Internal Audit program, including scheduling audits, ensuring timely response to findings, as well as metrics and trending
Development of Quality Metrics, and coordination of quality data collection and analyses for use in monthly metrics meetings and Management Reviews
Provide quality assurance support cross-functionally across the organization
Develop, implement, and manage Quality Control/Quality System process improvements.
Identify opportunities for improvement within the Quality System to ensure compliance and efficiency. Correct or improve gaps/opportunities in an independent fashion by writing and releasing new or revised Quality System documentation
Understand how and when to escalate quality issues to leadership team within the organization, presenting data and information necessary to draw conclusions and take action
Provide training and support to employees on quality processes and procedures
Support work on quality plans, quality processes
Minimum Qualifications:
Bachelor's Degree in Engineering, Biomedical Science, or other technical discipline preferred, with 3-6 years of relevant experience in medical device industry, including responsibility for Product Quality and/or Quality Systems
A working knowledge of Quality System Standards and regulations, including 21 CFR Part 820, ISO 13485, EU MDR
Preferred Qualifications:
Ability to multitask, handling multiple projects and changing priorities
Experience in the creation and documentation of procedures and processes
Must be results-driven and exhibit a sense of urgency
Proficiency with Microsoft Office - Word, Excel, PowerPoint and Access experience required
Ability to communicate ideas and information clearly, effectively, and frequently (both oral and written)
Ability to exercise independent judgment in methods, techniques, and evaluation criteria for obtaining results
Ability to act independently to determine methods and procedures
Problem-solving skills and the ability to resolve issues as they arise
Strong interpersonal skills, with the ability to assimilate with various cross-functional teams
Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship or employment visas currently.
NextPhase.ai is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.
Design Assurance Engineer (Only W2)
Manufacturing engineer job in Marlborough, MA
Job Title: Senior Design Assurance Engineer
Duration: 6 Months
Organizational Relationships: Works with Divisional personnel and Costa Rica personnel including R&D, Regulatory, Marketing, PMQA, Manufacturing Engineering, and Quality Engineering
Job Summary
• Provide design assurance support for new product development and on market medical devices. This role will be responsible to facilitate the application of design controls while supporting product development, manufacturing related design changes, maintaining regulatory compliance, implementing improvements for manufacturability and evaluating cost reduction efforts.
Essential Duties
Duties are listed in order of greatest importance. The incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as reasonably required by business needs.
• Participate independently on new product development project, assuring product inputs are clearly defined and assuring design verification and validation activities are appropriate and compliant to confirm inputs requirements are met. Test method validation would be an element of assuring verification/validation is acceptable.
• Participate independently on sustaining product projects, assuring project is clearly defined and stays on task, confirming product inputs are continuing to be met, and necessary verification, validation, and risk management activities are completed..
• Work collaboratively with R&D to coordinate design elements of Risk Management files for product to assure compliance with applicable standards and internal policies.
• Responsible for independently coordinating Health Risk Assessment team when needed for evaluation of on market product, must demonstrate efficient and effective analysis of situation, including problem definition and impact.
• Assess change requests of product for impact to design, determine supporting information required for implementation of changes.
Qualifications
Education
• Technical Bachelor Degree
Experience
• 2-5 years' experience preferably in medical device industry
Skills
• Experienced with FDA Quality System Regulations, especially Design Control requirements, ISO 13485 and Medical Device Directive
• Experienced with ISO 14970, Risk Management
• Familiarity with Usability, Reliability, Electrical Safety, Software, Sterilization, Packaging, and Biocompatibility standards and requirements.
• Working knowledge of verification and validation requirements for a regulated product
• Working knowledge of requirements analysis, including development of testable and measurable specifications
• Ability to effectively work on project teams, including taking leadership role on critical tasks to assure appropriate and timely completion/resolution
• Ability to appropriately assess written product and project documentation as the principle advocate for compliance, and ability to effectively communicate assessment
• Preferred:
o Working knowledge of test method validation, root cause failure analysis, statistical methods, and design of experiment
NPD Quality Engineer
Manufacturing engineer job in Plymouth, MA
Must Have Technical/Functional Skills
• Knowledge on Quality Management and its tools & techniques
• Knowledge about GMP (Good Manufacturing Practices), FDA, ISO 13485 and compliance regulations
• Knowledge on Medical Device Regulatory Standards, MDD and MDR
• Knowledge on NC, CAPA, Root Cause Analysis and Audit processes
• Knowledge on Validation process, writing protocols/ reports
• Very good understanding/ experience in writing procedures, product specs and work instructions
• Knowledge in Statistics, Risk Management and Design control
• Must possess good communication skills (verbal and written), familiar with project management methodology, problem solving, and presentation skills
• Experience in creating FMEAs & Writing reports
• Experience in PMS (Post Market Surveillance)
• Experience in PLM Tool (Windchill)
• Good understanding of Design, Drawing and GD&T
• Excellent Interpersonal / communication skills, Organizational / planning and Project management skills preferred
• Personal computer skills, Windows: word processing, presentation, e-mail, web browsers & spreadsheet software
• Ability to work efficiently, meet timelines, and communicate status (generate trackers, send emails, etc.)
Roles & Responsibilities
• Under limited supervision and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, the duties and responsibilities for this position are:
• Development and review of PDP (Product development Process) deliverables
• Review and approve R&D/ Engineering protocol/ reports
• Development of Risk management records (i.e. DFMEA/ PFMEA) in collaboration with SMEs
• Support and provide guidance on Validations and if required write Validation Protocols/ Reports
• Support/ Remediation of Validation/ Quality Documentation
• Support Root Cause Investigation and closure of NC and CAPA
• Review and approve the Change Orders (CR/ CN)
• Review and update the design/ process control documents like procedures/ work instructions/ product specs etc.
• Work with cross functional teams and internal teams to create deliverables
• Performs other duties assigned as needed
Salary Range: $90,000 $95,000 Year
TCS Employee Benefits Summary:
Discretionary Annual Incentive.
Comprehensive Medical Coverage: Medical & Health, Dental & Vision, Disability Planning & Insurance, Pet Insurance Plans.
Family Support: Maternal & Parental Leaves.
Insurance Options: Auto & Home Insurance, Identity Theft Protection.
Convenience & Professional Growth: Commuter Benefits & Certification & amp; Training Reimbursement.
Time Off: Vacation, Time Off, Sick Leave & Holidays.
Legal & Financial Assistance: Legal Assistance, 401K Plan, Performance Bonus, College Fund, Student Loan Refinancing.
Process Engineer
Manufacturing engineer job in Hopkinton, MA
WHO WE ARE
We are a leading cell and gene therapy contract development and manufacturing organization creating cutting-edge therapies that change people's lives. Join a company where collaborative, dedicated, and talented people are the backbone of our culture. Work both autonomously and in driven teams to make life-changing products utilizing ground-breaking science.
THE ROSLINCT WAY
Here at RoslinCT, our team contributes to the development of revolutionary treatments. We live every day by our core values: Partner Focus, One Team, Personal Growth, Integrity, Innovation, and Trust and Respect. We put our employees at the forefront by providing a flexible and empowering work environment, an attractive benefits package, and an emphasis on work-life balance. Our people are the key to our success. At RoslinCT we focus on developing our corporate culture, people's development, growth, and the ability to impact patients.
ACCELERATING YOUR FUTURE
The Process Engineer I/II will develop and execute technology transfer plans for RoslinCT's client processes, including working with key stakeholders in Manufacturing, Quality, Technology, and Operations departments. As a technical subject matter expert, the position will support routine production with troubleshooting, technical assessments of deviations, and product disposition evaluations. The position will play a key role in optimizing manufacturing processes and test methods, continuously improving quality, efficiency, and reliability while supporting products through clinical development to commercialization.
HOW YOU WILL MAKE AN IMPACT
Partner with colleagues in Operations, Quality Control, and Quality Assurance as well as external clients and suppliers to plan technology transfer, equipment setup and qualification, engineering and training runs, and process validation as applicable.
Support production and QC with process or equipment troubleshooting, deviation management, corrections and CAPA, as needed
Execute feasibility testing of new or alternative technologies and engage with key stakeholders to ensure technology development alignment with RoslinCT and Client program requirements
Collaborate with internal partners to experimentally determine key process and product monitoring and control attributes, analyze results and draft technical reports to communicate conclusions
Perform test runs and development studies as needed to support client and RoslinCT initiatives
Compile comprehensive data packages, operating procedures, and technical documentation to support technology transfer and process improvement
Be proactive in identifying opportunities to add value to processes and cross-functional teams
WHAT YOU WILL BRING
B.Sc. in Biological or Chemical Engineering (or similar) with 2-10 years of relevant process and/or analytical experience within the Cell and Gene Therapy or Biologics industry
Hands-on experience with aseptic manufacturing processes, cell culture, and process analytics
Experience with equipment support and troubleshooting
Demonstrated independence in experimental design, execution, data analysis, and troubleshooting
Preferred Qualifications
Advanced degree or additional certifications in science, engineering, or cGMP operations
Experience with bioreactor cell culture
Experience with cell selection, cell washing, lentiviral transduction, and cryopreservation
Experience with Microsoft Excel and statistical programs for data analysis and visualization
Excellent technical writing and oral communication skills
Driven and works well independently and within cross-functional teams
*May serve in an “on call” rotation to respond remotely to urgent issues (~1 week per month)
OUR COMMITMENT
All RoslinCT employees embrace the principles of our culture and values and are deeply committed to fostering an environment where diversity and inclusion are not only valued but prioritized. We believe a diverse and inclusive community empowers us to act courageously, care deeply, and dream boldly to impact people in big ways.
RoslinCT is proud to be an equal opportunity employer, we seek to create a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status, or any other applicable legally protected characteristics.
Applications Filtration Engineer
Manufacturing engineer job in Nashua, NH
About the Company
Critical Process Filtration, a TCPA Company, a leading manufacturer of high-quality filtration solutions for pharmaceutical, electronics, process water, and gas filtration is looking for a
Applications Filtration Engineer.
About the Role
The Applications Filtration Engineer will support the development, evaluation, and optimization of filtration technologies across a broad range of bioprocessing and industrial applications. This role plays a key part in shaping next-generation products through experimental research, customer application analysis, and cross-functional collaboration. The Applications Filtration Engineer will be responsible for designing studies, generating performance data, supporting product development, and ensuring our filtration solutions meet both technical and customer-driven requirements. This role offers the opportunity to contribute directly to innovative filtration solutions that serve high-growth global markets.
Responsibilities
Technology & Application Development
Support the development and characterization of filtration technologies including normal flow filtration, tangential flow filtration, and solid/liquid separation systems.
Design and execute laboratory experiments to assess filter performance, validate test methods, and evaluate new materials and device configurations.
Analyze performance data and use statistical tools to develop insights, optimize designs, and provide recommendations for product improvements.
Translate customer application needs into engineering requirements to guide internal R&D efforts.
Customer & Market Support
Partner with sales, marketing, and product management to provide technical expertise for key customer applications.
Assist in field evaluations, prototype testing, and troubleshooting to ensure optimal performance in customer processes.
Support the preparation of technical documentation, application notes, presentations, and training materials.
Cross-Functional Collaboration
Work closely with manufacturing, quality, regulatory, and engineering teams to ensure product readiness and alignment with customer expectations.
Participate in product development reviews and provide data-driven input on design, performance, and application requirements.
Engage with internal stakeholders to drive continuous improvement in test methods, product understanding, and application knowledge.
Innovation & Research
Identify emerging filtration technologies, materials, and methods that can enhance performance or open new market opportunities.
Contribute to intellectual property development, internal reports, and industry conference presentations.
Qualifications
Bachelor's, Master's, or PhD in Chemical Engineering, Biochemical Engineering, Biomedical Engineering, Mechanical Engineering, or another STEM discipline.
Relevant experience in biotechnology, bioprocessing, filtration, or related laboratory research.
Strong understanding of filtration principles, membrane technologies, or downstream bioprocessing.
Experience designing and conducting laboratory experiments and developing test methods.
Proficiency with statistical analysis, DOE, and data processing tools (e.g., Minitab, Excel, Python, MATLAB).
Familiarity with data acquisition systems, sensors, and laboratory instrumentation.
Knowledge of computational modeling or fluid dynamics (e.g., COMSOL) is a plus.
Effective communication skills with the ability to present technical information to multiple audiences.
Demonstrated problem-solving ability and a track record of technical accomplishments.
Equal Opportunity Statement
Critical Process Filtration is proud to be an equal opportunity employer.
EEO Statement: We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state/province, or local law.
Quality Engineer
Manufacturing engineer job in Portsmouth, NH
Alexander Technology Group is looking for a Quality Engineer for a client based in the Portsmouth, NH area.
This is full-time (perm)
On-site in Portsmouth, NH
Key Responsibilities:
Develop and maintain quality systems for combination products.
Ensure compliance with FDA, ISO 13485, cGMP, and other standards.
Lead risk assessments, root cause analyses, and corrective actions.
Oversee testing, validation, and documentation processes.
Collaborate with R&D, manufacturing, and regulatory teams.
Conduct training on QA practices and support continuous improvement.
Perform inspections and product testing to ensure quality standards.
Qualifications:
Bachelor's in Engineering, Life Sciences, or related field.
Strong knowledge of regulatory requirements and quality tools (e.g., Six Sigma, CAPA, FMEA).
Excellent problem-solving and communication skills.
Able to work independently in a small team environment.
Preferred:
Experience with design control, eQMS, and statistical tools.
ASQ CQE certification.
3+ years in QA/QE roles with combination products.
If interested, please send resume to ************************
Software Packaging Installation Engineer -- DAVDC5693544
Manufacturing engineer job in Natick, MA
Salary range: $87,100K P/A- $120,000 K P/A
Are you a Software Installation Engineer looking for a great new opportunity? Our Natick, MA client is looking to hire a Software Installation Engineer to package, deploy, maintain, and troubleshoot a variety of enterprise applications with a strong eye towards security. This will rely heavily on automation to ensure reliable and efficient delivery. This will involve everything from creation through to retirement, including updates, version control, delivery portal integration, and much more! This is a full-time, direct hire role.
Don't miss a great chance to join a large, stable, and growing company with a great work environment!
Must haves:
3+ years enterprise Network Engineer experience
Bachelors degree
InfoSec knowledge
InTune (or similar)
Work with cross functional teams
HM Notes:
App packaging
Security focused is needed - someone that has worked closely with infosec - not
active patching - automation
requests to bundle / configure / test / patching
InTune is one of the bigger tools
PatchmyPC is being used - but not widespread
Windows
Adding bandwidth? There are current fulltime people doing this - they're overloaded
Client JD:
The Software Installation Engineer is responsible for overseeing the packaging, deployment, maintenance, and troubleshooting of applications across the enterprise environment. This role ensures efficient and reliable delivery of approved software through automation tools and deployment systems, enabling a seamless experience for end users.
Responsibilities
Application Packaging & Deployment
Manage the full lifecycle of application packaging, from creation to deployment and retirement.
Ensure accurate version control, timely updates, and smooth integration with end-user delivery portals (e.g., Company Portal).
Maintain high standards of reliability and usability to support business workflows.
Tooling Administration
Administer and maintain application deployment and packaging tools that interface with user-facing systems.
Diagnose and resolve application packaging, deployment, and automation issues.
Collaborate with vendors and internal teams to implement fixes and enhancements.
Collaboration & Coordination
Partner with application requestors, Asset Management, and Legal teams to ensure compliance with software approval and licensing processes.
Work closely with cross-functional stakeholders to align deployment solutions with organizational standards and timelines.
Compliance & Security
Serve as the point of contact for Information Security to evaluate and block vulnerable or compromised applications.
Ensure compliance with internal policies and external security requirements.
Monitoring & Reporting
Track deployment performance, analyze data trends, and maintain portal reliability and responsiveness.
Minimum Qualifications
A bachelor's degree and 3 years of professional work experience (or a master's degree, or equivalent experience) is required.
Candidates for this position must be authorized to work in the United States on a full-time basis for any employer without restriction.
Visa sponsorship will not be provided for this position.
Additional Qualifications
Proficiency in application packaging and deployment, particularly with automation tools or scripting (e.g., PowerShell, PatchMyPC, WinGet).
Strong understanding of Windows operating systems, drivers, and enterprise deployment practices in a hybrid environment (cloud and on-prem).
Hands-on experience with management tools such as Intune, EntraID, AutoPilot, Active Directory and Group Policy.
Proven customer service experience with the ability to translate customer requirements into practical technical solutions.
Excellent analytical, problem-solving, and troubleshooting skills.
Strong written and verbal communication skills.
Familiarity with the mac OS platform is a plus.
Experience in enterprise environments.