Reliability engineer jobs in Cambridge, MA - 762 jobs

About LogRocket Founded in 2016, LogRocket's goal is to make every experience on the web as perfect as possible. We're solving a huge challenge for product managers and developers - understanding the user experience. LogRocket is the first system that gives these teams complete visibility into their customer's experience using their web apps - through pixel-perfect replays of user sessions and clear insight into logs, errors, and network activity. We've already attracted an elite roster of almost 3,000 customers including ClassPass, Capital One, Cisco, and Rippling, just to name a few. Our focus is on building software with care and craftsmanship and our engineering blog posts offer a taste of that. Backed by top investors such as Matrix Partners, Battery Ventures, and Delta-V Capital, we've raised $55M in funding and we're eager to bring talented people onboard to support our growth. We're on a mission to improve society's experience with software and that's where you come in. Responsibilities Improve quality of pager alerts while reducing noise Maintain awareness of engineering initiatives across the organization and monitor their impact on stability, cost, and performance Keep infrastructure up-to-date to take advantage of security patches and new features Improve operational security without sacrificing engineering independence Qualifications At least 4 years of experience as a Site Reliability Engineer, or related job Ability to read and understand product code (writing product code is a nice-to-have!) Familiarity with the state of the art in cloud technologies, including common providers, specific tools of the trade, and their strengths and weaknesses Experience operating applications and databases with demanding scalability or availability requirements Proven expertise in modern container orchestration practices (we use Kubernetes on GKE) A strong understanding of the performance, architecture, tooling, and cost of cloud systems A security focused mindset with a solid understanding of incident response and risk mitigation A strong collaborator who is transparent about progress on tasks, seeks feedback early and often, works effectively with the team and customers If you don't meet all of these, we still encourage you to apply. We believe that code is code, regardless of language, and learning different tools is part of joining a new company. Benefits & Perks Catered lunch and an impressive array of your favorite snacks (healthy AND non-healthy!) Unlimited vacation policy Health, Dental, Vision benefits, 401k, commuter benefits Generous stock options Regular team outings and activities (from boat rides to paintball, we'll try anything!) $135,000 - $220,000 a year This range is intended to provide a guideline for our typical compensation and may be modified based on location or experience of our finalist candidate. LogRocket is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. LogRocket will consider sponsoring visas for applicants in the US that need work authorization. #J-18808-Ljbffr

A technology company is seeking a Site Reliability Engineer in Boston to enhance cloud-native services and ensure high reliability. Responsibilities include building foundational platforms, utilizing cloud tools, and following best practices. Candidates should have over 5 years of relevant experience in managing cloud platforms and programming languages like Python or Go. This role follows a hybrid work schedule, promoting collaboration and innovation. #J-18808-Ljbffr

Plant Reliability Engineer page is loaded## Plant Reliability Engineerremote type: Fully Onsitelocations: Tuscola, ILtime type: Full timeposted on: Posted 4 Days Agojob requisition id: R25\_000005Cabot Corporation (NYSE: CBT) is a leading global specialty chemicals and performance materials company headquartered in Boston, Massachusetts, USA. Our businesses deliver a broad range of products and solutions to customers in every corner of the globe, serving the transportation, infrastructure, environment and consumer industry sectors. We bring the power of innovative chemistry to solve customers' challenges today while preparing them to meet tomorrow's needs. Our commitment to innovation is driven by a passion to advance our customers' businesses through our deep understanding of their applications and the global trends that impact their operations. If you do not meet every requirement, or your experience is slightly different that what we have listed, we still encourage you to apply! Cabot has an exciting opportunity for a Plant Reliability Engineer to join the team. This person will provide technical support and drive continuous improvements in manufacturing functions including production, packaging, and warehouse processes. They will help to improve capability, capacity and productivity at the site to ensure safe and optimal process utilization. They will implement capital and expense projects within scope, cost, time, and safety standards as well as identify and execute improvements in equipment reliability and process safety management.The Plant Reliability Engineer will work on-site at the Tuscola, IL plant. **How You Will Make an Impact:**• Identify, recommend and implement improvements in plant performance to optimize product rates, yields, and quality in accordance with business needs and in alignment with SH&E requirements. • Provide technical support to resolve problems. Use statistical techniques to improve process capability and control. Use failure analysis methodologies to identify root causes. Recommend and implement solutions. Work in collaboration with cross functional departments to achieve company goals. • Provide support for the site mechanical integrity program by investigating equipment issues and eliminating the recurrence of failures that will improve plant performance and reliability. Review maintenance work plans to ensure optimum preventative maintenance scheduling and maintenance work practices. Develop Asset Care Plans to monitor the condition of plant equipment to maximize plant safety and reliability to reduce downtime. • Assist in the design, procurement, and installation of new equipment. Recommend, develop, and coordinate capital improvements. Support and implement new product and process development. Create manufacturing Standard Operating Procedures for process and equipment operation. • Conduct “end-of-life” assessments making recommendations for equipment repairs and replacements. Identify and implement improvements in equipment monitoring capabilities. • Serve as Process Safety Management (PSM) custodian for manufacturing in coordination with site and regional PSM representatives in the evaluation of manufacturing process-related risks and incidents. Participate in Process Hazards Analysis (PHA) for key manufacturing and capital projects. Ensure all product and process changes are implemented in line with appropriate Management of Change (MOC) principles. Provide training as required for manufacturing personnel. • Monitor maintenance and capital projects and external contractors in accordance with all site regulations and standards. • Support efforts to implement and maintain the Responsible Care Management System in line with the requirements of the RC14001 technical specification. **What You Will Bring to Cabot:**• Knowledge of chemical manufacturing process technologies, engineering principles, mechanical and instrumentation systems, calibration and maintenance, and local and distributed control systems. • Knowledge of Root Cause Failure Analysis (RCFA) methodologies and reliability analysis tools. • Knowledge in areas such as confined space entry, lockout-tag-out, hot-work permitting, etc. • Statistical analysis and equipment diagnostic skills. • Project management skills including scheduling, safety oversight, and contractor management.• Bachelor/University degree in a relevant Engineering discipline. • Minimum 2+ years' experience in an appropriate manufacturing environment.**How We'll Support Your Success:**• Pay and Benefits - The salary range for this role is from $86,500 to $119,000. The actual compensation offered to the successful candidate will depend on the candidate's skills, qualifications, experience, and location. This role is eligible for comprehensive benefits on the first day of employment and an annual discretionary bonus based on company performance.• Dynamic, Flexible, Hard Working, Team Environment - We are busy, collaborative, growing, and we are doing really meaningful work. • Growth -Training, great peer coaching and support, and the ability to personally grow your influence, your position, and your compensation. • Meaningful Work that is Valued - Customers are demanding sustainable solutions without compromising quality or performance. The work we do is visible, and is helping to create a more abundant, affordable, and cleaner future. It is an awesome feeling to know you're making a living by making a positive impact in the world; and to be able to say, “I was a part of that.” • Feedback - we are committed to giving and receiving feedback in a direct and open fashion. • Support - you are part of a team and deserve to feel encouraged and supported. You will be part of a team that cares about you personally and professionally. Our success depends on your success.#LI-Onsite#CINDAt Cabot, we bring the power of innovative chemistry and a spirit of partnership with our customers to advance solutions that will enable a sustainable future. Our strength in research and development is a major reason why we have been an industry leader for more than 135 years in products such as reinforcing and specialty carbons, battery materials, aerogel, fumed metal oxides, inkjet colorants, masterbatches and conductive compounds. Our employees around the world are united by our shared purpose: Creating materials that improve daily life and enable a more sustainable future. Through our corporate strategy, “Creating for Tomorrow,” we are focused on our core strengths to lead in performance and sustainability - today and into the future.***EEO/AA Employer/Vet/Disabled/RC14001** Realizing we function better together than individually, Cabot Corporation is proud to be an equal opportunity employer. We are committed to fostering an inclusive culture that embraces our differences and to empower employees to achieve exceptional results, without consideration of sex, race, color, religion, national origin, citizenship, age, disability, marital or veteran status, sexual orientation, gender identity or expression, or any other legally protected categories. This includes providing reasonable accommodation for employees' and applicants' disabilities or religious beliefs and practices, in accordance with applicable law.**Cabot is committed to supporting and maintaining a safe and environmentally focused working environment. All employees are expected to uphold this commitment in every position.****Nondiscrimination Policy with Respect to Discussion of Pay** This is to advise that it is the policy of Cabot Corporation not to discharge or in any other manner discriminate against any employee or applicant for employment because such employee or applicant has inquired about, discussed, or disclosed the compensation of the employee or applicant or another employee or applicant. This policy, however, shall not apply #J-18808-Ljbffr

The Role Cimulate is seeking a skilled Site Reliability Engineer to join our dynamic team as we revolutionize the future of commerce through intelligent, AI‑driven systems. In this pivotal role, you'll own the reliability, availability, and performance of our SaaS production environment-monitoring critical systems, managing deployments, and ensuring seamless operations for our customers. As a Site Reliability Engineer, you'll manage production support processes, deployments (including model releases), and incident response, with an opportunity to grow the role into managing vendor partners for 24/7 follow‑the‑sun coverage. This position combines hands‑on technical problem‑solving with process ownership and operational leadership. Your work will directly contribute to the stability and scalability of Cimulate's AI platform, supporting our mission to help businesses operate and engage more intelligently. Responsibilities Ensure reliability, availability, and performance of SaaS production systems and AI pipelines. Monitor production environments, deployed models, and data pipelines; respond rapidly to incidents and service disruptions. Manage deployments, configuration changes, and release processes (e.g., model and service rollouts). Maintain and enhance observability, monitoring, and alerting systems (e.g., Grafana, Prometheus, ELK). Lead incident response, postmortems, and continuous improvement of operational processes and playbooks. Partner with DevOps and engineering teams to improve scalability, fault tolerance, and automation. Track and improve reliability metrics (SLAs, SLOs, SLIs). Create and maintain clear technical documentation, including runbooks and escalation paths. Participate in on‑call rotation and drive improvements in incident management and response. Grow into managing vendor teams providing 24/7 L1 operational coverage. Requirements Proven experience in monitoring and supporting production systems, preferably in a SaaS or multi‑tenant environment. Strong knowledge of Linux systems and scripting (Python, Bash, or Go). Hands‑on experience with cloud platforms (GCP preferred; AWS/Azure also valuable) and container orchestration (Kubernetes, Docker). Familiarity with Infrastructure‑as‑Code (IaC) tools such as Terraform or Pulumi. Understanding of networking, databases, and performance tuning. Experience with observability, monitoring, and logging tools (Grafana, Prometheus, ELK, etc.). Proficiency with Git, version control workflows, and CI/CD pipelines. Strong analytical, debugging, and problem‑solving skills. Excellent communication and collaboration abilities, including with non‑technical stakeholders. Calm under pressure and effective in incident management situations. Growth mindset with the ambition to build and lead scalable 24/7 production operations. Nice to haves Experience working with security, compliance, or audit frameworks. Exposure to AI/ML pipelines or data‑driven systems. Prior experience managing offshore or vendor‑based support teams. Why Join Cimulate? Work with a passionate and collaborative founding team Make a real impact at an early‑stage startup with high‑growth potential Help redefine the future of online shopping and personalization Competitive compensation, equity, and benefits #J-18808-Ljbffr

Boston Red Sox and Fenway Sports Management Type: Full-time Salary: Not disclosed Members of the Baseball Systems team at the Boston Red Sox are focused on designing, building, and refining the software and data pipelines used within Baseball Operations. These tools and applications are an integral part of the decision‑making process, are directly integrated in the workflows of all departments within Baseball Operations, and provide an efficient, consistent, and accessible experience when interacting with our internal data sources and applications. POSITION OVERVIEW The DevOps & Site Reliability Engineer, Baseball Systems position will be a member of the baseball operations software development team and is responsible for the cloud operations and automation supporting all Baseball Operations systems. This individual will work closely with members of baseball operations to understand business requirements that drive the analysis, design, and long‑term roadmap of a best‑in‑sport automation and cloud operations framework. This position is responsible for Azure operations, deployment automation, and will collaborate closely with colleagues on the software development team and baseball operations personnel from all departments. RESPONSIBILITIES Design, build, and maintain robust and scalable cloud infrastructure on Azure, including virtual machines, containers, storage, and networking. Develop and implement automation solutions using tools such as Terraform, Ansible, or Azure DevOps to streamline infrastructure provisioning, configuration management, and deployments. Build and maintain continuous integration and continuous delivery (CI/CD) pipelines using Azure DevOps or similar tools. Monitor and troubleshoot production systems, identify and resolve performance bottlenecks, and implement proactive measures to prevent outages. Collaborate with development teams to improve software delivery processes, promote best practices, and ensure system reliability. Participate in on‑call rotations and provide timely support for production issues. Stay up‑to‑date with the latest technologies and trends in cloud computing, DevOps, and SRE. COMPETENCIES Aptitude and ability to document and create frictionless CI/CD pipelines. An understanding of general engineering practices in the collaboration of achieving performant cloud solutions & DevOps practices. Ability to pick up quickly and think both creatively and critically to solve problems. A basic understanding of contemporary baseball and/or sports analysis and development practices. A team‑player that collaborates effectively with technical and non‑technical stakeholders. ADDITIONAL QUALIFICATIONS 3+ years of experience in a DevOps or SRE role. Strong experience with Azure cloud platform services, including compute, storage, serverless functions, APIs, and security. Proven experience in building and maintaining CI/CD pipelines using tools like Azure DevOps, Github Actions, or similar. Proficiency in scripting languages such as Python or Bash for automation tasks. Experience with infrastructure‑as‑code tools such as Terraform, Ansible, or Puppet. Strong understanding of networking concepts, including VPCs, subnets, routing, and security groups. Experience with containerization technologies such as Docker and Kubernetes. Experience with integration with Slack. Excellent communication and collaboration skills. Strong problem‑solving and analytical skills. In addition to the above requirements, all roles within Baseball Operations are expected to effectively demonstrate our universal competencies related to problem solving, teamwork, clarity of communication, and time management, along with embodying our culture of honesty, humility, relentlessness, and commitment to DEIB. #J-18808-Ljbffr

**Role Number:** 200*********** Imagine what you could do here. At Apple, new ideas have a way of becoming extraordinary products, services, and customer experiences very quickly. Bring passion and dedication to your job and there's no telling what you could accomplish. Dynamic, smart people and inspiring, innovative technologies are the norm here. The people who work here have reinvented entire industries with all Apple Hardware products. The same passion for innovation that goes into our products also applies to our practices strengthening our commitment to leave the world better than we found it. Join us to help deliver the next groundbreaking Apple product. Are you passionate about changing the world? We have a critical impact on getting high quality functional products to millions of customers quickly. You will be working with a team of expert C programmers on system level validation (correctness, performance, and debugging) of video compression sub-systems in silicon. **Description** As part of the silicon validation team, you will perform block and system-level validation of video compression subsystems in Apple silicon. Work with designers and architects to understand the operation of hardware video compression blocks at the block and system levels. Participate in architecture and design specification review Investigate the use cases, system-level operation, and performance requirements. Develop low-level software to validate functionality, conformance, and performance of video compression blocks. Participate in the hardware video compression blocks validation on simulator, emulation, FPGA and silicon. Work with other members of the validation team to incorporate your tests into system-level tests. Bring-up and debug devices on new hardware platforms. **Minimum Qualifications** + A minimum of a bachelor's degree and a minimum of 3 years of relevant industry experience in silicon validation software engineering or related field **Preferred Qualifications** + Knowledge of video standards such as H.264/AVC, HEVC, and AV1. + Experience with hardware compression engines is a plus. + Solid programming skills in C/C++ Experienced with embedded systems programming + Device driver experience a plus. Apple is an equal opportunity employer that is committed to inclusion and diversity. We seek to promote equal opportunity for all applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, Veteran status, or other legally protected characteristics. Learn more about your EEO rights as an applicant (*********************************************************************************************** .

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

Vaxess is developing a pipeline of next-generation therapeutics on our novel micro-array patch platform. With only five minutes of wear-time on the skin, the Vaxess' patch combines room 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. 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 At Vaxess, we're bringing together exceptional talent to drive our product development forward. We value collaboration, curiosity, and a dynamic work environment. To apply, please submit your CV/resume to ******************.

Job Title: Process Engineer Duration: February 2026 - December 2028 Commitment: Full-time (40 hours/week) - On-Site with minimal travel The Process Engineer will support a major capital project involving the design and construction of a new Oral Solid Dosage (OSD) manufacturing facility. Responsibilities include equipment procurement, installation, start-up, and commissioning. The engineer will act as an equipment package owner and serve as the primary technical resource for the project, including assisting with validation activities. Key Responsibilities Collaborate with project stakeholders, equipment vendors, site engineering, and automation teams. Develop equipment bid packages (URS, data sheets, specifications). Manage equipment purchasing activities from procurement through delivery. Support facility design and construction activities. Participate in the equipment CQV lifecycle: Conduct design reviews and risk assessments. Create and execute commissioning protocols. Support validation protocol approval and execution. Maintain required training and contribute to documentation and protocol development. Travel to vendor locations as needed for project activities. Required Experience Extensive experience in an OSD cGMP environment. Proven project delivery experience with: Isolators, Downflow booths, Material handling systems (powder-related) Experience with at least one of the following: Granulation systems (wet and dry), Tablet compression systems, Tablet coaters, Packaging lines (primary and secondary)

About the job Title: Project Engineer - Automation of Machinery and Processes Employment Type: Contract Duration: 12+ months Status: Accepting Candidates About the role The Senior Project Engineer will lead the design, development, and implementation of automated machinery and process systems. This role partners closely with Engineering, Manufacturing, Quality, and cross-functional stakeholders to deliver compliant, efficient, and scalable equipment solutions in regulated environments. Key Responsibilities • Oversee the design, specification, and selection of automated equipment systems in alignment with project objectives and industry standards • Act as system Subject Matter Expert (SME) during design reviews, commissioning, qualification, and validation activities • Lead process improvement initiatives and implement change controls to enhance equipment systems and manufacturing processes • Manage key equipment development deliverables, including URS, FRS, and technology transfer documentation • Develop, review, and maintain critical documentation such as protocols, reports, and SOPs to ensure regulatory compliance • Collaborate with cross-functional teams to successfully execute equipment development and manufacturing projects • Provide hands-on troubleshooting and technical support for rapid development cycles and manufacturing sustainability • Execute project activities on time and within budget; proactively communicate risks, delays, and issues to stakeholders • Ensure compliance with regulatory, corporate, and quality system requirements, including deviation management, CAPA, and change control activities • Perform other duties as assigned Qualifications • Bachelor's degree in Engineering or a related technical discipline • Strong experience with automation of machinery and manufacturing processes • Hands-on experience supporting equipment commissioning, qualification, and validation • Working knowledge of regulated environments (GxP preferred) • Proven ability to manage documentation, change controls, and cross-functional collaboration Compensation (MA Pay Transparency): • Estimated hourly range: $70-$75/hr (W-2) • Final rate within this range will be based on skills, experience, and interview results

Join a Team Where Engineering Excellence Drives Opportunity At Affiliated Engineers, Inc. (AEI), we bring together expertise and innovation to solve the most complex challenges. Since 1978, we've supported mission-driven organizations in designing sy Project Engineer, Project, Engineer, Process Engineer, Systems, Construction, Business Services, Process

A leading biotechnology company in Boston is looking for a Principal Engineer to lead automation of the data QC and reporting processes. The ideal candidate will have extensive experience in technical leadership, particularly in the biotechnology sector, with advanced programming skills in R and Python. Responsibilities include developing modernization initiatives and leveraging AI solutions to improve data management and reporting standards. This position allows for a hybrid work model, requiring up to 10% travel. #J-18808-Ljbffr

& Responsibilities The Senior Process Engineer Technical Services is responsible for driving overall process technology implementation initiatives, continuous improvement / optimization programs, and leading innovation as it relates to Radius shredders, joint products, and other ferrous and non-ferrous operations. Improving yields, product quality and developing new product streams is a key pillar of the technical services department strategy and as such, this role is a key role in ensuring Radius' success in delivering on improved production metrics, throughput, product quality, sustainable low carbon products and reducing environmental footprint. Essential Functions Play a key role in implementing the metal recovery technology strategy and other technological improvements across the Radius enterprise. Project manage the overall execution of technology, continuous improvement and capital projects, ensuring proper resources are identified and assigned, projects are scoped and scheduled, and progress is monitored and managed. Lead process improvement and technological advancements in recycling with the goals of enhancing product quality, increasing metal recovery (reduce/divert landfill), help in creating new product streams (plastics, tires, and other adjacencies), and growing process efficiencies (throughput, mechanical availability, etc.). Establish and maintain necessary relationships and contracts with third party service providers, engineering firms, contractors, and consultants to ensure initiatives are appropriately engineered and adequately resourced. Act as a technical resource to the management teams (shredder, JP, maintenance, etc.) to assist with any technical opportunities that arise during operations. Leverage existing systems as well as define and establish new improved systems and processes. Ensure project budgets are effectively and efficiently utilized and met. Develop and deliver training and support tools for operations to institutionalize new technologies and process improvements. Assist in the development of fiscal year capital plans for any of the continuous improvement or reliability projects, including but not limited to, major maintenance projects, outages and others. Provides process training to employees as necessary. Work closely with Environmental, Health & Safety teams to ensure adherence to all Radius policies and procedures as well as identify opportunities for sustainability improvements and reducing impact on the environment. Ensuring a safe work environment for all employees, customers and visitors. Internal Control Responsibilities Supports Internal Control process which includes understanding, communicating, and complying with defined internal controls as well as suggesting and making modifications to the policies, procedures, and controls to better match the business. Communicates upward problems in operations, noncompliance with the code of conduct, or other policy violations or illegal actions. Interpersonal Contacts The Senior Process Engineer - Technical Services will be required to develop and maintain effective working relationships with Technical Services peers, the Operations team including Operations Managers (Shredder, Shear, Balers and Joint Products), Regional Managers, Purchasing Managers, Maintenance Managers at Radius facilities. The role will also be required to develop and maintain effective relationships with preferred service providers, equipment suppliers and contractors. Job Conditions This position will require frequent travel, up to 60% of the time. Visits to yards in each region can be expected to be under all weather conditions. Physical hazards may be present due to the equipment and machinery used throughout the recycling facility and the presence of the scrap itself. This position may require work beyond normally scheduled hours at times to support operations. Qualifications Bachelor's degree in an Engineering Field and 5 years of process engineering and project management experience; or equivalent combination of education, job experience and knowledge. Previous experience in the scrap metals recycling industry or an adjacent heavy industry (e.g., mining, gas & oil, municipal waste recycling, heavy fabrication & processing) is desirable. Experience leading and implementing continuous improvement / optimization projects. In addition, a keen drive for safety at work and understanding of environmental permitting processes. This position requires possession of a valid driver's license and the ability to drive an automobile. Ideal Competencies Ability to apply logical principles to solve practical problems and deal with many variables and determine a specific course of action. Ability to analyze data, to develop effective strategies from such analysis, and to translate these strategies into effective actions at the operational level. Accountability Integrity Customer Focus Use of functional expertise Teamwork Physical Requirements And Work Environment Able to: travel domestically and internationally, sit, stand, or walk for up to 6-8 hours per day; bend, crouch; climb, balance, push/pull, lift or carry up to 50 pounds. Able to write by hand and keyboard for extended periods of time. Communication is primarily by phone, email and in person, with other departments within the Radius Group. Visual acuity is needed for close detail work, preparing and analyzing data figures, accounting, and computer use.

A leading healthcare technology firm is hiring Machine Learning Engineers to develop and deploy AI models for enhancing patient outcomes. Candidates should have strong backgrounds in Python and machine learning frameworks, with an emphasis on collaboration across scientific and engineering teams. The ideal candidates are those with a passion for improving healthcare through innovative solutions. This role presents a unique opportunity to directly impact patient care while working on advanced ML projects and initiatives. #J-18808-Ljbffr

Circuit Technology Center is a national leader in high reliability circuit board rework, repair, and modification. We support aerospace, defense, medical, and advanced technology customers who rely on us to solve complex board level challenges that require deep technical judgment and hands on expertise. We are hiring an Electronics Process Engineer, SMT & Rework to support our production and engineering teams. This role is ideal for an engineer with hands on electronics manufacturing or SMT experience who wants to deepen their expertise in board level rework, thermal processes, and high reliability electronics. This is a hands on, shop floor focused role working closely with experienced technicians on complex assemblies. What You'll Do Support SMT and rework process setups including thermal profiling, airflow control, and heat management Assist with hot air and rework system setup for complex assemblies Evaluate circuit boards for repairability, component sensitivity, and rework risk under guidance Support troubleshooting of SMT and rework related defects and failures Help interpret schematics, BOMs, drawings, and technical documentation Assist with process documentation, work instructions, and continuous improvement efforts Work directly with technicians to support safe, repeatable, and reliable rework processes What You Bring 2 to 8 years of experience in electronics manufacturing, SMT, process engineering, or related fields Hands on exposure to SMT assembly, reflow, or board level processes Basic understanding of thermodynamics, heat transfer, and component sensitivity Ability to read and interpret schematics and technical documentation Comfort working on the shop floor and supporting technicians Strong curiosity, problem solving mindset, and willingness to learn from senior engineers Preferred Experience Experience in aerospace, defense, medical, or other high reliability electronics environments Exposure to hot air rework systems, reflow ovens, x ray inspection, or failure analysis Familiarity with IPC standards such as IPC A 610, J STD 001, or IPC 7711 7721 This role offers hands on exposure to complex electronics, close mentorship from senior engineers, and the opportunity to grow into deeper technical ownership over time.

A leading technical solutions provider is seeking an engineer specialized in the medical device industry. The role involves designing manufacturing processes and ensuring compliance with safety regulations. Candidates should have a BBA in Engineering, knowledge in CSV, and problem-solving skills (Yellow or Green Belt). The position offers an opportunity to work with innovative technologies in a dynamic environment located in Caguas, Puerto Rico. #J-18808-Ljbffr

A leading global biotechnology firm in Boston seeks a Principal Engineer to lead the automation of pre-clinical data pipelines and regulatory reporting solutions. This role focuses on driving modernization and standardization initiatives, leveraging AI technologies, and enhancing data consumption practices. Candidates should possess strong programming skills and a degree in a relevant field, with a minimum of five years in technical leadership within the biotechnology industry. The position offers a hybrid work model and a comprehensive benefits package. #J-18808-Ljbffr

Who We Are: At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented and diverse workforce in our industry. Our commitment to uncompromising focus on quality, compliance, safety, and excellence in delivery shapes everything we do. We are not just looking for skills; we are seeking innovative individuals who have a mindset open to learning and growth, and a desire to make a difference. Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility, we develop solutions and processes that support and accelerate innovation. Join us on our mission to enable current and next-generation therapeutics to improve and save the lives of patients. Role Overview: This role serves as the site SME for all cleaning validation and verification activities related to intermediate and API manufacturing, including facility surfaces and equipment. You'll work closely with cross-functional teams to ensure regulatory compliance and implement effective cleaning strategies that meet customer expectations. This position is key to maintaining high quality and safety standards across manufacturing operations. Additionally, you'll manage the environmental and purified water monitoring programs to ensure consistent product quality throughout the process. Core Responsibilities: Lead the development, execution, and validation of cleaning procedures for equipment, production lines, and facilities. Write and review cleaning validation protocols and reports in compliance with regulatory requirements, ensuring that all materials are free of any residues or contaminants. Coordinate and conduct sampling (e.g., swab, rinse, and surface) and analytical testing to validate cleaning processes and confirm cleaning effectiveness. Develop and maintain cleaning validation schedules to ensure timely completion of required validations Review cleaning validation data, ensuring it meets established acceptance criteria, and make recommendations for process improvements. Qualifications: Required Minimum 7 years of quality assurance experience with an undergraduate degree in engineering, science or related field Minimum of 3 years of experience in contamination control, cleaning validation, environmental monitoring, and/or purified water systems, preferably in a pharmaceutical or biotech manufacturing environment (API CDMO experience is highly desirable) Proven leadership experience in pharmaceutical, API/intermediate, medical device, biologics or related FDA industry Strong knowledge of cGMP, FDA, EMA, ICH guidelines, and other regulatory standards related to contamination control, cleaning validation, environmental monitoring, and purified water systems Experience with microbiological sampling, environmental monitoring, and testing of purified water systems in a regulated pharmaceutical environment Proficiency with risk assessment tools such as FMEA Previous experience working in cross-functional and project-based environments Experience creating metrics for driving continuous improvement Excellent analytical, written and verbal communication and presentation skills and a mindset that promotes a positive work culture Hands-on experience with cleaning validation, TOC analysis, and bioburden reduction strategies Driven and detail-oriented, with a strong understanding of cGMP regulations and previous experience in cleaning validation Experience driving complex projects with the ability to initiate, prioritize, and successfully complete tasks Proven experience working effectively in team situations and as an individual contributor Demonstrated behaviours that model the Veranova culture to achieve an inclusive environment and exceptional business results The ideal candidate will have hands-on experience with sterile and cleaning validation processes, strong technical writing skills, and the ability to execute validation protocols independently Experience in a fast-paced work environment Preferred Certification in contamination control (e.g., PDA Certification in Contamination Control). Knowledge of risk-based approaches to cleaning validation (e.g., Risk Assessment and ICH Q9) Experience with continuous improvement methodologies such as Lean or Six Sigma desire Familiarity with environmental monitoring equipment and purified water system design and validation Salary Range : $90,000 - $100,000 annual base salary Our Commitment: Health & Wellness: Comprehensive health & wellness benefits. Access to mental health resources and wellness programs. Generous PTO and holiday pay policies. Financial Wellness: Veranova is committed to fair and transparent compensation practices. This includes a competitive base salary, eligibility for performance-based bonuses, and an attractive 401(k) Plan with company match. Salary ranges reflect the scope and expectations of the role, and are based on market data, internal equity, and role-specific factors. Final compensation may vary depending on experience, skills, education, and business needs. Professional Development: Opportunities for continuous learning through LinkedIn Learning, workshops, conferences, and mentorship. Tuition Assistance for Undergraduate and Graduate degree programs. Inclusive Culture: At Veranova, an inclusive culture is integral to our values. We welcome people with diverse experiences and perspectives who share our mission to improve and save lives. Even if you don't meet every qualification, we encourage you to apply. Veterans, first responders, and those transitioning from military to civilian life bring valuable skills that strengthen our team. Additional Information: Applicants for this role must be authorized to work in the United States without further employer sponsorship. Agency and Search Firm Representatives: Veranova does not accept unsolicited resumes from agencies and/or search firms for this job posting. All your information will be kept confidential according to EEO guidelines. Veranova is an Equal Opportunity Employer. It is the policy of Veranova to provide equal employment access and opportunity to all persons regardless of age, race, color, national origin, religion, sex, sexual orientation, gender identity and/or expression, physical or mental disability, genetic information, citizenship, marital status, veteran status, or any other characteristic protected by federal, state, or local law. All applications are carefully considered, and your details will be stored on our secure Application Management System. This is used throughout Veranova for the selection of suitable candidates for our vacancies as they arise. Veranova respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice .

A leading specialty chemicals company is seeking a Plant Reliability Engineer to join their team in Tuscola, IL. This role focuses on providing technical support and driving continuous improvement in manufacturing processes. The ideal candidate will have a relevant degree and experience in a manufacturing environment, emphasizing safety and efficiency. Responsibilities include investigating equipment issues, improving reliability, and collaborating with cross-functional teams to optimize plant performance. Strong project management and statistical skills are essential. #J-18808-Ljbffr