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Job Description We're seeking a Senior Process Engineer who's ready to be part of a company committed to formulating everyday success for every customer through innovative, reliable products used to adhere, seal, and protect at every level of the building envelope. ABOUT THE ROLE We are seeking an experienced and highly motivated Process Project Engineer to both manage capital improvement projects and provide direct technical support to our manufacturing operations. The ideal candidate is a hands-on engineer with a strong background in chemical process environments. In addition to managing the entire project lifecycle-from scope definition to commissioning-this role will be a key technical resource for the site, responsible for driving continuous improvement by analyzing workflows, identifying bottlenecks, and optimizing existing processes to enhance safety, quality, and efficiency. This position requires a unique blend of technical engineering acumen, project management discipline, and a practical, plant-floor perspective. We are hiring in Houston, TX, Rockland, MA, and Waukesha, WI. WHAT YOU'LL BE DOING Project Lifecycle Management: • Lead capital projects from initial concept and feasibility studies through design, procurement, installation, commissioning, and final documentation., • Develop detailed project scopes, schedules, and cost estimates ($)., • Manage multiple projects simultaneously, providing regular status updates to stakeholders. Process Optimization & Plant Support: • Analyze production data, workflows, and processes to identify bottlenecks, inefficiencies, and opportunities for improvement., • Develop and implement data-driven solutions to improve product quality, increase operational efficiency, and enhance process safety., • Lead and support continuous improvement initiatives and root cause analysis investigations for production and safety-related issues., • Provide daily technical support to Operations and Maintenance teams to troubleshoot process upsets and ensure stable, reliable production. Technical Design & Equipment Specification: • Read, interpret, and modify Piping & Instrumentation Diagrams (P&IDs)., • Perform engineering calculations to properly size and specify process equipment, including pumps, piping, vessels, valves, and instrumentation., • Research and identify the best available equipment and technology for specific applications., • Ensure all designs comply with internal standards and relevant industry codes (e.g., ASME, API). Procurement & Vendor Management: • Develop comprehensive Request for Quotation (RFQ) packages for equipment and services., • Perform technical and commercial bid analyses to select suppliers and contractors., • Visit supplier sites to conduct equipment trials and Factory Acceptance Tests (FATs)., • Perform Site Acceptance Tests (SATs) when equipment has arrived onsite. Construction & Contractor Management: • Vet, select, and manage on-site contractors for all installation and construction activities., • Lead safety orientations and ensure all on-site work is performed in strict adherence to company safety protocols (e.g., Lockout/Tagout, hot work permits)., • Ensure that all local, state, and federal rules and regulations are followed during construction (building permits, modification of PSM or RMP, etc.)., • Provide direct on-site supervision to ensure equipment is installed and erected according to engineering specifications and best practices., • Commission equipment and work directly with other functions such as operations, maintenance, and quality to ensure that equipment meets design standards., • Work in cross-functional teams to create Standard Operating Procedures (SOPs), follow Management of Change (MOC) protocol, and provide/create equipment documentation where necessary. Maintenance & Reliability Integration: • Apply a "Design for Maintainability" mindset to all projects, ensuring safe and efficient access for future maintenance and repairs., • Collaborate with the Maintenance and Reliability teams to identify critical spare parts, develop preventative maintenance plans, and ensure a smooth handover of project documentation. WHAT WE ARE LOOKING FOR Education: • Bachelor of Science in Chemical Engineering (Required), • Master of Science in Chemical Engineering (Preferred) Experience: • Minimum of 5-7 years of combined project and process engineering experience in a chemical manufacturing environment., • Proven track record of managing "cradle-to-grave" capital projects from $50K to $5M+., • Demonstrated experience in process optimization, troubleshooting, and continuous improvement in a manufacturing setting., • Direct, hands-on experience with the specification, installation, and startup of process equipment (pumps, piping, tanks, control systems)., • Demonstrated experience in managing and directing contractors and skilled trades., • Experience in a maintenance or reliability role is a strong plus., • Experience working in a PSM and RMP regulated environment. Skills & Abilities: • High proficiency in reading and creating P&IDs, Electrical Schematics, Construction Plans, and other technical drawings., • Strong analytical and problem-solving skills with a data-driven approach to decision- making., • Knowledge of continuous improvement methodologies (e.g., Lean, Six Sigma) and root cause analysis tools., • Strong understanding of process control fundamentals (DCS/PLC)., • Excellent communication skills, with the ability to effectively interact with plant operators, maintenance technicians, and senior management., • A robust safety mindset and knowledge of OSHA and industry safety standards., • Proficiency with MS Project or similar project scheduling software., • Experience with AutoCAD or other CAD software is desirable. WHAT WE OFFER • Competitive Compensation, • Retirement Savings, • Medical, Dental, Disability and Life Insurance Coverage, • Holistic Health & Well-Being Programs, • Health Savings Accounts (HSA) & Flexible Spending Accounts (FSA) for, • Health and Dependent Care, • Vision and other Voluntary Benefits and Discounts, • Paid Time Off and Holidays, • Paid Parental Leave (Maternity and Paternity), • Educational Assistance Program #BuildingEnvelope Amrize is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We thank all applicants for their interest; however, only those selected for an interview will be contacted. BUILDING INCLUSIVE WORKSPACES At Amrize, there is endless opportunity for you to play your part. Whether you're in a technical, managerial, or frontline role, you can shape a career that works for you. We're seeking builders, creative thinkers and innovators. Come put your expertise to work while developing the knowledge and skills to drive your career forward. With us you'll have the chance to build your ambition! Amrize North America Inc. takes pride in our hiring processes and our commitment that all qualified applicants will receive consideration for employment without regard to age, race, color, ethnicity, religion, creed, national origin, ancestry, gender, gender identity, gender expression, sex, sexual orientation, marital status, pregnancy, parental status, genetic information, citizenship, physical or mental disability, past, current, or prospective service in the uniformed services, or any other characteristic protected by applicable federal, state or local law. Amrize North America Inc, and its respective subsidiaries are Equal Opportunity Employers, deciding all employment on the basis of qualification, merit and business need. Amrize Canada Inc. is committed to the principles of employment equity and encourages the applications from women, visible minorities, and persons with disabilities. In compliance with the ADA Amendments Act (ADAAA), if you have a disability and would like to request accommodation in order to apply for a position with us, please email . This email address should only be used for accommodations and not general inquiries or resume submittals. In Ontario, our organization/business is committed to fulfilling our requirements under the Accessibility for Ontarians with Disabilities Act. Under the Act, accommodations are available on request for candidates taking part in all aspects of the selection process. While we sincerely appreciate all applications, only candidates selected for an interview will be contacted.]]>

Job DescriptionDescription: ABOUT ELEKTROFI Elektrofi is revolutionizing the delivery of biologic therapies by giving patients the ability to control how they want to receive and benefit from life-changing medicines. Our breakthrough ultra-high concentration microparticle technology platform resolves the limitations associated with intravenously administered biologic therapies by enabling convenient at-home subcutaneous self-administration. With a focus on monoclonal antibodies, therapeutic proteins, and other biologics, we partner with companies to develop and commercialize our novel Hypercon™ formulations. We believe a patient-centered healthcare approach can lead to a healthier world. We are headquartered in Boston and innovate globally. We are Formulating the Future of Biologics™. POSITION SUMMARY Elektrofi is seeking a motivated individual to join our biotech company as a Director of Engineering to support the design, fabrication, and qualification of our novel aseptic microparticle formulation platform. The Head of Engineering is a highly skilled and experienced technical engineering leader who will lead and manage stakeholders cross-functionally both internally and externally. The work for this role is highly matrixed with the complexity of working on several capital projects in parallel as the company executes the 5-year manufacturing strategy for projected growth. This role will be responsible for overseeing the planning, execution, and successful delivery of capital engineering projects. The ideal candidate will have a strong background in engineering management, process engineering design, excellent leadership capabilities, and a proven track record of driving project success. Experience with multi-million-dollar capital projects and having a PE (Professional Engineer) License is preferred. The role will serve as an interface between Program Management, Process Development, MS&T, Quality, Supply Chain, and Legal for internal, partner, and CDMO stakeholders. Global travel up to 30% of the time may be required during startup of new manufacturing sites to support technology transfer. The individual should thrive in a fast-paced and dynamic environment and be a key player in the company’s growth. The individual will join a growing, multidisciplinary team of scientists/engineers and industry professionals. KEY RESPONSIBILITIES • Leadership and Management: Provide strategic direction and leadership for the project engineering & process engineering projects, ensuring alignment with company goals and objectives., • Project Oversight: Oversee the planning, scheduling, and execution of engineering projects, ensuring they are completed on time, within scope, and budget., • Stakeholder Communication: Act as the primary point of contact for project stakeholders, including partners, upper management, and cross-functional teams, ensuring clear and effective communication., • Resource Allocation: Manage and allocate resources effectively to optimize project execution and team performance., • Risk Management: Identify potential risks and develop mitigation strategies to ensure project success and minimize impact., • Quality Assurance: Ensure all projects meet the highest quality standards, adhering to industry regulations and company policies., • Design, Fabrication, Qualification: Ensure all DQ, IOQ, AOQ, and commissioning activities are completed to company or partner standards., • Continuous Improvement: Drive continuous improvement initiatives to enhance project processes, tools, and methodologies., • Education: Bachelor’s degree in mechanical or chemical engineering, or a related field. MS/MENG preferred., • Experience: 10+ years of experience in engineering project management, with at least 5 years in a leadership role., • Technical Expertise: Strong technical background in engineering principles and practices, pharmaceutical industry experience is preferred., • Leadership Skills: Proven ability to lead & inspire a project team of engineers and project managers., • Travel: up to 30% travel to equipment suppliers, CDMOs, and partner sites may be required., • Project Management: Extensive experience in managing complex engineering projects, equipment qualification, including budgeting, scheduling, and resource allocation., • Communication: Excellent verbal and written communication skills, with the ability to effectively interact with stakeholders at all levels., • Problem-Solving: Strong analytical and problem-solving skills, with the ability to make sound decisions under pressure., • Adaptability: Ability to adapt to changing priorities and manage multiple projects simultaneously., • General Knowledge of ISO, FDA CFR, EMA Annex 1 standards for GMP manufacturing., • Experience managing external engineering firms and fabrication shops., • Strong understanding of lean manufacturing, DQ, IOQ, automation and process validation., • Ability to conduct FMEA analysis. Create, review, and approve P&IDs and 3D equipment models. EEOC Statement: Elektrofi provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. To all agencies, please, no phone calls or emails to any employee of Elektrofi about this requisition. All resumes submitted by search firms/employment agencies to any employee at Elektrofi via email, the internet, or in any form and method will be deemed the sole property of Elektrofi unless such search firms/employment agencies were engaged by Elektrofi for this requisition and a valid agreement with Elektrofi is in place. If a candidate submitted outside of the Elektrofi agency engagement process is hired, no fee or payment of any kind will be paid. All candidates must be legally authorized to work in the US. #LI-Onsite

Job Description InnoTECH Staffing is looking for a Product Development Engineer I for a company in the Boston, MA area. There is no sponsorship available and requires being onsite 5 days a week. Product Development Engineer / Scientist We are seeking a Product Development Engineer/Scientist to join our talented and diverse technical team in Malden, MA. This position will focus on developing novel coatings platforms from lab-to-scale to address customer needs. A bachelor’s degree or higher in Mechanical, Chemical or Electrical Engineering, Chemistry, Materials Science, or associated technical field is required. Fluency in Mandarin, Spanish, or German preferred but not required. Candidate must be legally allowed to work in the US. Key Responsibilities • Develop novel coating platforms, test metrics, and design experiments by working in a lab-based environment with minimal day-to-day guidance., • Develop hypotheses and conduct experiments to improve understanding and performance of company's coating technology by coordinating with various team members., • Communicate technical advances internally with other members of the company and interact with external vendors, independent testing laboratories, and customers to explain and troubleshoot application of the technology., • Support scaling of coating from lab or pilot scale to a manufacturing environment., • Collaborate with sales or technical service to address customer requests., • Expand company's coating portfolio by innovating on current coating technology and developing new coating platforms. Our client is a dynamic materials technology company in Malden, MA. With a strong global technical team, they develop and manufacture coatings that protect printed circuit boards in electronics, allowing them to function in water-laden environments. They work with the biggest brands in the consumer electronics and automotive industries to increase product reliability and improve product performance in wet and humid conditions. Not only do they provide a portfolio of coatings, but they also work closely with their customers to help solve some of their most difficult problems through rapid innovation and ingenuity. The salary range for this position is $75,000 – $90,000 per year.

Job DescriptionDescription: ABOUT ELEKTROFI Elektrofi is revolutionizing the delivery of biologic therapies by giving patients the ability to control how they want to receive and benefit from life-changing medicines. Our breakthrough ultra-high concentration microparticle technology platform resolves the limitations associated with intravenously administered biologic therapies by enabling convenient at-home subcutaneous self-administration. With a focus on monoclonal antibodies, therapeutic proteins, and other large molecule drugs, we create, develop, and commercialize subcutaneous biologic therapies in collaboration with strategic partners. We believe a patient-centered healthcare approach can lead to a healthier world. We are headquartered in Boston and innovate globally. We are Formulating the Future of Biologics ™. POSITION SUMMARY Elektrofi is seeking a motivated individual to join our biotech company as a Sr. Engineer II to support the development of our novel Hypercon™ formulation platform. This individual will lead and support the technical execution of platform process development activities across a diverse portfolio of partner programs. As Sr. Engineer II you will contribute deep technical expertise across one or more unit operations, ensure scalability of platform processes, and serve as a critical link between development, manufacturing, and external partners. This role is ideal for an experienced engineer ready to lead cross-functional efforts, mentor junior staff, and drive platform adaptability to meet evolving program needs. The individual will join a growing, multidisciplinary team of scientists/engineers and industry professionals. Key Responsibilities • Design and execute platform and program process development studies including mixing, TFF, sterile filtration, and filling., • Serve as a technical lead on development workstreams supporting platform improvement and tech transfer to GMP manufacturing site., • Analyze data, identify trends, and define critical process parameters and critical quality attributes., • Author and review technical documentation including protocols and reports to support CMC regulatory submissions., • Interface with Manufacturing Sciences & Technology (MSAT), QA, Analytical, and partner-facing teams to align technical deliverables., • Mentor junior engineers and contribute to the growth of technical and operational best practices., • Support continuous improvement of the platform to enhance scalability, robustness, and program flexibility., • Identify and follow through on opportunities for innovation and continuous improvement in the drug product manufacturing process, and lead initiatives aimed at improving process knowledge and scale-up strategies., • Provide direct management oversight of 1-2 technical personnel., • B.S. in Chemical, Biomedical, Materials, or Pharmaceutical Engineering, or a related engineering discipline w/ 8+ years of relevant experience in process development or biomanufacturing, or M.S. w/6+ years or Ph.D. w/2+ years of relevant experience., • Demonstrated ability to lead process development and cross-functional projects., • Proven technical and strategic leadership in cross-functional teams and ability to communicate with stakeholders and partners., • Experience with cGxP and aseptic manufacturing is required., • Experience with novel platform development is preferred., • Experience developing biologic drug products or parenteral suspensions is preferred., • Experience in processes involving ATEX, Class I Div I, Class I Div II equipment design is a plus., • Experience with single-use systems (SUS), filtration technologies, Downstream biologic DS purification, Aseptic Drug Product manufacturing, Fill/Finish or CIP/SIP., • Familiarity with platform process design, scalability principles, and QbD methodologies., • Strong communication skills and comfort working with internal stakeholders and external partners. EEOC Statement: Elektrofi provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. To all agencies, please, no phone calls or emails to any employee of Elektrofi about this requisition. All resumes submitted by search firms/employment agencies to any employee at Elektrofi via email, the internet, or in any form and method will be deemed the sole property of Elektrofi unless such search firms/employment agencies were engaged by Elektrofi for this requisition and a valid agreement with Elektrofi is in place. If a candidate submitted outside of the Elektrofi agency engagement process is hired, no fee or payment of any kind will be paid. All candidates must be legally authorized to work in the US. #LI-Onsite

Job Description About Us Eden is pioneering sustainable natural resource recovery by using electricity to enhance subsurface permeability. Our Electrical Reservoir Stimulation technology offers a precise, water-efficient alternative to traditional hydraulic fracturing, reducing environmental risks while maximizing resource extraction. Backed by leading public and private institutions, we have raised ~$24M, including $14M in dilutive capital from industry leaders such as Anglo American and Helmerich & Payne, along with climate-focused investors like the Grantham Foundation. Additionally, we have secured $10M in non-dilutive funding, primarily through four DOE ARPA-E grants that support our R&D in frontier industries. Headquartered in Somerville, MA, and with an office in Houston, TX, Eden's team of 16 experts specializes in geophysics, geochemistry, high-voltage engineering, and subsurface tool design. We are actively demonstrating our next-generation permeability enhancement technology across diverse geologies worldwide, collaborating with industry leaders in geothermal energy, geologic hydrogen, carbon storage, and mining to redefine resource recovery for a carbon-neutral future. Looking ahead, we are preparing for surface and subsurface field tests, in cooperation with our supportive technical partners. Your Impact • Develop and refine 3D reservoir models in Petrel from geologic interpretations, incorporating gridding, upscaling, and facies modeling to capture heterogeneity and optimize simulation accuracy., • Distribute petrophysical properties and integrate natural and induced fractures using DFN, dual-porosity, and Embedded Discrete Fracture Models to achieve realistic subsurface representations., • Design and execute hydraulic fracture simulations in Kinetics, calibrating permeability, connectivity, and fracture geometry for high-fidelity results., • Configure and run full-field thermal recovery simulations in Intersect to evaluate Enhanced Geothermal System (EGS) performance, including cold-water injection and heat extraction modeling., • Simulate thermal-hydraulic-mechanical-chemical (THMC) coupling to assess long-term reservoir behavior, fracture evolution, and energy recovery sustainability., • Partner with geologists, geomechanical engineers, and field teams to integrate multi-disciplinary data, validate models, and optimize stimulation strategies., • Identify and quantify key reservoir uncertainties through sensitivity analysis, guiding field development and design decisions. About You • Master’s or PhD (or equivalent expertise) in Petroleum, Reservoir, or Geothermal Engineering, or a closely related subsurface discipline., • 3+ years of experience building and running 3D reservoir models and full-field simulations, ideally within geothermal or unconventional systems., • Strong command of Petrel, Kinetics, and Intersect for model construction, upscaling, fracture integration, and thermal recovery simulation., • Proficient in fracture modeling and geomechanics, including stress analysis, fracture propagation, and permeability evolution under coupled THMC conditions., • Deep understanding of thermal recovery mechanisms, heat transfer physics, and flow behavior in high-temperature reservoirs., • Experience with discrete fracture network (DFN), dual-porosity, and Embedded Discrete Fracture Models (EDFM) to capture reservoir heterogeneity and fracture connectivity., • Skilled in gridding, upscaling, and petrophysical property modeling to balance computational performance and simulation accuracy., • Analytical thinker capable of interpreting complex field and laboratory data, performing sensitivity analyses, and optimizing model performance., • Collaborative, detail-driven engineer who thrives in multi-disciplinary environments bridging geoscience, geomechanics, and field operations. Preferred but Not Required • Experience with Enhanced Geothermal Systems (EGS) or coupled thermal-hydraulic-mechanical-chemical simulations., • Familiarity with fracture closure effects, stress anisotropy, and reservoir stimulation strategies., • Background in startup, R&D, or applied innovation environments with hands-on model iteration and fast experimental feedback loops. Eden is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunities regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. If you have a disability that requires accommodation, please let us know by emailing admin (at) edengeopower.com

Job DescriptionCompany Description CRB's nearly 1,400 expert professionals drive innovative, life-changing and life-saving solutions for manufacturers in the life sciences and food and beverage industries. Our mission, vision, and core values put client satisfaction and employee experience at the center of everything we do. As an AEC firm, we proudly specialize in industries that inherently carry important social responsibility - we recognize our impact and influence in the communities we serve and pursue corporate responsibility through the lens of people, community, and planet. From oncology and rare disorders to COVID-19 or alternative proteins, our design and construction projects are pioneering solutions addressing important issues such as food scarcity and global health. Job Description We are actively seeking a Process Engineer Intern to join CRB. Join our firm for an internship journey where you’ll dive into real-world project work, learn from industry leaders and fully immerse yourself in the CRB employee experience. This program is more than just an internship—it's an opportunity to grow, innovate, and make a tangible impact on how we do business. You’ll have the chance to work hands-on with cutting-edge projects, collaborate with peers and industry leaders, and contribute your unique perspective to spark meaningful change. At CRB, we believe that learning should be as dynamic as it is engaging, and that work can be both challenging and enjoyable. Join us to expand your horizons, build lasting relationships, and experience what it truly means to be part of a team that’s dedicated to innovation and excellence. How will I contribute? As a Process Engineer Intern, you will work under the direction of an assigned Process Engineer mentor to develop and implement project deliverables. Project sizes will vary and consist mainly of pharmaceutical, biotech, food and beverage, or industrial projects including existing building renovations/retrofits and new construction. Our Process engineering team focuses on the design and engineering of manufacturing facilities and equipment, supporting facility infrastructure and critical utility systems. They are responsible for supporting the documentation of the process design scope in coordination with other disciplines. Core Responsibilities • Developing project documents and deliverables such as:, • Block & Process Flow Diagrams, • User Requirements Specifications, • Equipment List, • Equipment General Arrangements, • Equipment Datasheets, • Utility Summary, • Piping and Instrumentation Diagrams, • Plans, schedules, and installation details and specifications in coordination with manufacturing partners and trade partners, • Assisting with the development of conceptual designs and coordinating with the design team under the direction of the project manager, • Work with cross-functional teams, including architects, engineers and construction to ensure seamless project execution. Communicate findings and recommendations effectively to stakeholders.Qualifications Qualifications: • Currently pursuing a Bachelor's or Master's degree in Mechanical Engineering, Chemical Engineering, Bioprocess Engineering, or Biochemical Engineering from an accredited program, • Available to work full-time during the internship period: May–August 2026, • Proficiency in Microsoft Office Suite (Outlook, Word, Excel, PowerPoint, OneNote), • Strong interest in the Food & Beverage or Life Sciences industries, • Excellent problem-solving skills with the ability to analyze complex data and develop actionable insights, • Strong communication and collaboration skills, with the ability to work effectively across disciplines and with internal and external stakeholders (vendors, clients, contractors), • Eagerness to learn about the AEC industry and apply academic knowledge to real-world engineering applications, • Working towards Fundamental of Engineering Exam registration or completion preferred, • Familiarity with AutoCAD, Revit and 3D collaboration tools (Navisworks, BIM360 Suite, Assemble), • Experience with process optimization and lean manufacturing principles, • Familiarity with industry-specific regulations and standards within the AEC industry, • Prior internship or co-op experience in Process Engineering or related field Additional Information All your information will be kept confidential according to EEO guidelines. CRB is committed to hiring and retaining a diverse workforce. We are proud to be an Equal Opportunity/Affirmative Action Employer and it is our policy to provide equal opportunity to all people without regard to race, color, religion, national origin, ancestry, marital status, veteran status, age, disability, pregnancy, genetic information, citizenship status, sex, sexual orientation, gender identity or any other legally protected category. Employment is contingent on background screening. CRB does not accept unsolicited resumes from search firms or agencies. Any resume submitted to any employee of CRB without a prior written search agreement will be considered unsolicited and the property of CRB. Please, no phone calls or emails. CRB offers a complete and competitive benefit package designed to meet individual and family needs. If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Job DescriptionCompany Description CRB is a leading provider of sustainable Engineering, Architecture, Construction and Consulting solutions to the global life sciences and food and beverage industries. Our 1,100 employees provide best-in-class solutions that drive success and positive change for our clients, our people and our communities. CRB is a privately held company with a rich history of serving clients throughout the world, consistently striving for the highest standard of technical knowledge, creativity and execution. Job Description The Lead Process Utilities Engineer is responsible for overseeing the discipline at a project level and managing the project discipline budget on simple to complex projects of all sizes. The Lead Engineer has a thorough understanding of the development and field implementation of documents across all project phases. The Lead Engineer possesses the ability to coordinate with internal and external parties, manage multiple complex tasks, establish priorities and direct the work of others. The Senior Engineer has a thorough understanding of the development and field implementation of documents through all project phases, sizes and levels of complexity. The Senior Engineer possesses the ability to coordinate with internal and external parties, manage multiple complex tasks, establish priorities and direct the work of others. This position has the ability to be based near our offices in Philadelphia, Maryland, or Boston. Core Activities • Plans and directs work and manages a project budget from a discipline design perspective on large complex projects., • Works with Project Manager on proposal development, man-hour planning and project scheduling for the discipline scope of work on intermediate level projects., • Leads interactions with clients, internal stakeholders and external partners., • Oversees the discipline at a project level and manages the project discipline budget on simple to complex projects of all sizes., • Conducts quality checking of documents for complex projects (e.g., technical verification of design calculations and documentation) and drives overall project quality., • Coordinates with internal and external parties, manages multiple complex tasks, establishes priorities and directs the work of others., • Develops and delivers intermediate level internal discipline design and engineering training presentations., • Directs and manages the workflows and execution of design and engineering support staff (Entry-Level to Senior) to meet client expectations and project goals., • Oversees the production of deliverables or leads activities which require more experience, deeper understanding or involve more complexity such as:, • Layout Development for Utility Rooms, • Space Planning for Pipe Routing, • Capacity Planning/Expansion Strategy, • Complex Vendor Package Management, • Participation in or facilitation of Risk Assessments, HAZOPs / HCCPs / Etc., • 3D Model Review and Coordination, • Site Walkdowns and Field Reports, • Commissioning and StartupQualifications Minimum Qualifications • ABET-accredited Bachelor’s degree in in chemical / mechanical engineering, • Minimum of 10 years of experience for Lead position, • Minimum of 15 years of experience for Senior position, • A mixture of design firm, operating company or construction related experience (within the market sector), • Professional Engineering License, • Effective leader with excellent written and verbal communication skills, • Diversity of experience across a variety of facilities, equipment and systems used in the life sciences industry Additional Information All your information will be kept confidential according to EEO guidelines. #LI-Hybrid CRB is committed to hiring and retaining a diverse workforce. We are proud to be an Equal Opportunity/Affirmative Action Employer and it is our policy to provide equal opportunity to all people without regard to race, color, religion, national origin, ancestry, marital status, veteran status, age, disability, pregnancy, genetic information, citizenship status, sex, sexual orientation, gender identity or any other legally protected category. Employment is contingent on background screening. CRB does not accept unsolicited resumes from search firms or agencies. Any resume submitted to any employee of CRB without a prior written search agreement will be considered unsolicited and the property of CRB. Please, no phone calls or emails. CRB offers a complete and competitive benefit package designed to meet individual and family needs. If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process. CRB is committed to hiring and retaining a diverse workforce. We are proud to be an Equal Opportunity/Affirmative Action Employer and it is our policy to provide equal opportunity to all people without regard to race, color, religion, national origin, ancestry, marital status, veteran status, age, disability, pregnancy, genetic information, citizenship status, sex, sexual orientation, gender identity or any other legally protected category. Employment is contingent on background screening. CRB does not accept unsolicited resumes from search firms or agencies. Any resume submitted to any employee of CRB without a prior written search agreement will be considered unsolicited and the property of CRB. Please, no phone calls or emails. CRB offers a complete and competitive benefit package designed to meet individual and family needs. If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Job Description Job Title: Senior Scientist/Engineer - Process Development & Upstream Manufacturing Location: Boston, Massachusetts Department: Bio process Development / Manufacturing Sciences Reports To: Director of Process Development or Head of Manufacturing Position Summary: We are seeking a highly motivated and experienced Senior Scientist or Engineer to lead upstream process development activities for biologics manufacturing. This role will focus on the design, optimization, and scale-up of cell culture processes for therapeutic proteins, monoclonal antibodies, or other biologics. The ideal candidate will bring deep technical expertise in upstream bio processing, strong project leadership skills, and a collaborative mindset to drive innovation and operational excellence. Key Responsibilities: Process Development • Design and execute experiments to optimize upstream processes including media development, feeding strategies, and bio reactor operations., • Develop scalable processes for mammalian or microbial cell culture, ensuring robustness and reproducibility., • Evaluate and implement new technologies to improve yield, productivity, and product quality., • Lead scale-up activities from bench to pilot and GMP manufacturing scales., • Collaborate with Manufacturing, Quality, and Regulatory teams to ensure seamless tech transfer and process implementation., • Work closely with downstream, analytical, and formulation teams to ensure end-to-end process integration., • Participate in CMC strategy development and contribute to project timelines and risk assessments., • Analyze complex data sets using statistical tools and modeling software., • Maintain detailed records of experimental work in electronic lab notebooks (ELNs)., • Ph.D. in Chemical Engineering, Biochemistry, Biotechnology, or related field with 5+ years of industry experience; or M.S. with 8+ years., • Proven track record in upstream process development for biologics., • Hands-on experience with bio reactors (ambr, bench-scale, pilot-scale), cell culture systems, and process analytics., • Familiarity with QbD principles, DoE, and regulatory expectations for biologics manufacturing., • Experience with microbial fermentation or continuous processing., • Knowledge of PAT tools and automation systems., • Prior involvement in IND/BLA submissions or regulatory inspections., • Be part of a cutting-edge team advancing next-generation biologics., • Work in a collaborative, innovation-driven environment.

Job DescriptionDescriptionPosition: Process Design Engineer Overview Verdox, Inc. is dedicated to reversing climate change through the development and deployment of advanced technology. Our proprietary electro-swing process, developed at MIT, enables carbon dioxide and other acid gasses to be captured with up to 80% less energy and 70% less cost than conventional approaches. We are backed by institutional investors and based in Boston. Verdox seeks to hire a highly motivated Process Design Engineer to support plant design for applications utilizing our electro-swing absorption system. Key Responsibilities • Prepare design basis and engineering packages for pilot plant, demonstration plant, and commercial plant, which include PFDs, P&IDs, and process simulation modeling, • Incorporate all elements required for a successful plant build, including utilities requirements, site considerations, environmental permitting, operational considerations, performance requirements, regulatory requirements, and applicable design standards, • Apply principles of mass and heat transfer to process and equipment design, including conceptual design, FEED, and detailed engineering, • Work closely with R&D, manufacturing, product development, and business development to understand requirements, specifications, and deliver unified view of plant design, • Works with engineering consultants to finalize P&IDs, plot plans, electrical one-lines, equipment lists, I&CS, and equipment specs, • Perform process hazard and operable analysis (HAZOP), incorporating key safety and environmental risks and mitigations, • Bachelor's degree in Chemical Engineering or Process Engineering, • 5-10 years of progressive experience in project design, management, preferable on large capital projects, • Working knowledge of process modeling and equipment design, such Aspen HYSYS or the like, • Critical thinking and decision-making skills with ability to synthesize inputs and distill issues to recommendation to key stakeholders, • Ability to work well with cross-functional teams and with demonstrated interpersonal skills in establishing internal and external working relationships, • Start-up attitude - adapting to changing priorities, thriving in small cross-functional teams, and delivering impactful results Experience in chemical, gas, process or refinery plant EPC and commissioning is a plus

Job Description InnoTECH Staffing is looking to hire a fulltime / permanent Senior Materials Scientist / Engineer who has at least 3 years of coatings product development experience for a fast-growing and well funded coatings company in the Boston area. !!! Must be a US Citizen or Greencard Holder !!! This position will focus on developing new platform technologies (organic / polymers) for environmental protection and implementing at customers. ** Any additional languages (Mandarin, German and Spanish) are a plus, but not required. Some international travel required. Responsibilities for this role include: ● Developing functional materials, test methods, and implementation solutions for addressing environmental protection of electric vehicles, ADAS systems, and consumer electronics. ● Maintaining project plans, timelines, and deliverables for staying accountable on product launch strategy. ● Communicating technical advances and project strategy internally across a global team comprising technical team members and sales. ● Working autonomously on open-ended projects ranging from new coating development to creation of novel application techniques. ● Expanding Company’s intellectual property portfolio by innovating on current or new coatings and application technology. ● Serving as the subject matter expert on coatings under development and participating in developing strategy for implementing coating solution at customer. ● Collaborating effectively with various functions within sales, technical services, manufacturing, and operations on new product launch. ● Mentoring technicians and co-ops on execution of experiments towards coating development. Candidate must be legally allowed to work in the US. *** International and domestic travel is required. Education: M.S. or Ph.D. in Mechanical Engineering, Chemical Engineering, Chemistry, Materials Science, or Electrical Engineering or associated technical field. Previous industry or research experience development of coatings preferred. Depending on skills and experience, this role is paying up to $125K base and also has a bonus and full benefits package

Job DescriptionCompany Description At CRB, we design and build some of the most powerful facilities in the world — those that change people's lives. We are the leading provider of sustainable Engineering, Architecture, Construction and Consulting solutions to the global life sciences and food and beverage industries. Our employees provide best-in-class solutions that drive success and positive change for our clients, our people and our communities. CRB is a privately held company with a rich history of serving clients throughout the world, consistently striving for the highest standard of technical knowledge, creativity and execution. Job Description The Entry-Level Process Engineer focuses on the design and engineering of manufacturing facility and equipment, supporting facility infrastructure and critical utility systems. Typical tasks include execution of engineering calculations including heat transfer and pressure drop calculations. The Entry-Level Process Engineer is responsible for supporting the documentation of the process design scope in coordination with other disciplines. The Entry-Level Process Engineer may support field installation teams and execute construction site observations. This role is expected to work closely with other architects, engineers and designers, as well as other internal and external team members to ensure a coordinated, constructible and complete design. Core Activities * Supports the documentation of the process design scope in coordination with other disciplines. * Works closely with other architects, engineers and designers, as well as other internal and external team members to ensure a coordinated, constructible and complete design. * Self-checks own work but communicates often with peers and Supervisor. * Able to work on one or more projects concurrently and manage time effectively. * Solves complex problems under the direction and supervision of a mentor or supervisor * Project work may include all levels of design such as studies, conceptual and schematic design, design development, construction documentation and construction administration. Works on matters of basic complexity in a support role under the direction of more experienced Process Engineers. Engineering deliverables include: * Block and Process Flow Diagrams * User Requirements Specifications * Equipment List * Equipment General Arrangements * Equipment Datasheets * Utility Summary * Piping and Instrumentation Diagrams (P&IDs) Qualifications • Bachelor’s degree in Mechanical, Chemical, or Bioprocess Engineering from an ABET-accredited program, • 0–3 years of experience in a design firm or related engineering environment, • Registration for or successful completion of the Fundamentals of Engineering (FE) exam preferred, • Willingness to relocate to one of our office locations: Massachusetts (MA), Pennsylvania (PA), Orange County (OC), San Diego (SD), or St. Louis (STL) Preferred Qualifications * Fundamental experience with performing engineering calculations, developing and implementing list of discipline systems designs * Fundamental experience with chemistry/biochemistry * Fundamental experience with process modeling, material and energy balances and basic sizing calculations * Fundamental experience with fluid mechanics, hydraulic modeling and fundamental heat transfer * Strong communication skills and ability to participate in internal cross-discipline project team coordination * Proficient at fundamental discipline design calculations under the supervision of an engineer * Proficiency in AutoCAD * Proficiency in Microsoft Office suite required * Proficiency in engineering software applications including computer-aided drafting, process modeling and calculation programs Additional Information All your information will be kept confidential according to EEO guidelines. CRB is committed to hiring and retaining a diverse workforce. We are proud to be an Equal Opportunity/Affirmative Action Employer and it is our policy to provide equal opportunity to all people without regard to race, color, religion, national origin, ancestry, marital status, veteran status, age, disability, pregnancy, genetic information, citizenship status, sex, sexual orientation, gender identity or any other legally protected category. Employment is contingent on background screening. CRB does not accept unsolicited resumes from search firms or agencies. Any resume submitted to any employee of CRB without a prior written search agreement will be considered unsolicited and the property of CRB. Please, no phone calls or emails. CRB offers a complete and competitive benefit package designed to meet individual and family needs. If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Job DescriptionSenior Product Development Engineer/Scientist About actnanoWe are a dynamic materials technology company in Malden, MA. With a strong global technical team, we develop and manufacture coatings that protect printed circuit boards in electronics, allowing them to function in water-laden environments. We work with the biggest brands in the consumer electronics and automotive industries to increase product reliability and improve product performance in wet and humid conditions. Not only do we provide a portfolio of coatings, but we also work closely with our customers to help solve some of their most difficult problems through rapid innovation and ingenuity. About this RoleWe are seeking a Senior Product Development Engineer/Scientist to join our talented and diverse technical team in Malden, MA. This position will focus on developing new platform technologies for environmental protection and implementing at our customers around the world. A master’s or doctorate in Mechanical, Chemical or Electrical Engineering, Chemistry, Materials Science, or associated technical field is required. Fluency in Mandarin, Spanish, or German preferred but not required. Candidate must be legally allowed to work in the US. Key Responsibilities • Develop functional materials, test methods, and implementation solutions for the environmental protection of automotive and consumer electronics., • Maintain project plans, timelines, and deliverables related to product launch strategy., • Communicate technical advances and project strategy to a global team of technical and sales personnel., • Work autonomously on open-ended projects, from new coating development to novel application techniques., • Expand actnano’s IP portfolio by innovating on coatings and application technology., • Serve as the subject matter expert on coatings and participate in developing customer implementation strategies., • Collaborate with cross-functional teams and maintain project plans, timelines, and deliverables for product launches., • Mentor technicians and co-ops on conducting experiments for coating development., • International and domestic travel is required.This position is based in Malden, MA, accessible via the Orange Line. The salary range for this position is $115,000 – $125,000 per year, which reflects the base pay the Company reasonably and in good faith expects to pay at the time of this posting. Powered by JazzHR T2HGUzK02S

Job DescriptionProduct Development Engineer/Scientist About actnanoWe are a dynamic materials technology company in Malden, MA. With a strong global technical team, we develop and manufacture coatings that protect printed circuit boards in electronics, allowing them to function in water-laden environments. We work with the biggest brands in the consumer electronics and automotive industries to increase product reliability and improve product performance in wet and humid conditions. Not only do we provide a portfolio of coatings, but we also work closely with our customers to help solve some of their most difficult problems through rapid innovation and ingenuity. About this RoleWe are seeking a Product Development Engineer/Scientist to join our talented and diverse technical team in Malden, MA. This position will focus on developing novel coatings platforms from lab-to-scale to address customer needs. A bachelor’s degree or higher in Mechanical, Chemical or Electrical Engineering, Chemistry, Materials Science, or associated technical field is required. Fluency in Mandarin, Spanish, or German preferred but not required. Candidate must be legally allowed to work in the US. Key Responsibilities • Develop novel coating platforms, test metrics, and design experiments by working in a lab-based environment with minimal day-to-day guidance., • Develop hypotheses and conduct experiments to improve understanding and performance of actnano’s coating technology by coordinating with various team members., • Communicate technical advances internally with other members of the company and interact with external vendors, independent testing laboratories, and customers to explain and troubleshoot application of the technology., • Support scaling of coating from lab or pilot scale to a manufacturing environment., • Collaborate with sales or technical service to address customer requests., • Expand actnano’s coating portfolio by innovating on current coating technology and developing new coating platforms., • Some international and domestic travel required. This position is based in Malden, MA, accessible via the Orange Line. The salary range for this position is $75,000 – $90,000 per year, which reflects the base pay the Company reasonably and in good faith expects to pay at the time of this posting. Powered by JazzHR I3Y9Z3UrYH

Job Description Job Summary: The Process Validation Engineer is responsible for planning, executing, and documenting process validation activities to ensure that manufacturing processes consistently produce products meeting quality and regulatory requirements (FDA, GMP, ISO 13485). The role involves working cross-functionally with Manufacturing, Quality, and R&D teams to support new product introductions, process improvements, and ongoing validation maintenance. Key Responsibilities: • Develop and execute Process Validation (PV) protocols (IQ/OQ/PQ) in compliance with regulatory standards., • Support Equipment Qualification and Cleaning Validation as needed., • Conduct risk assessments (FMEA) and establish critical process parameters and acceptance criteria., • Perform data analysis and summarize validation results with clear conclusions and recommendations., • Prepare and maintain validation documentation, reports, and master plans., • Collaborate with manufacturing and quality teams to identify and resolve process issues., • Ensure compliance with cGMP, FDA, ISO 13485, and company validation policies., • Support change control and CAPA processes related to validated systems., • Participate in internal and external audits by providing validation documentation and responses. Required Qualifications: • Bachelor’s degree in Engineering (Mechanical, Chemical, Biomedical, or related field) or equivalent., • 3 years of experience in process validation within the pharmaceutical or medical device industry., • Strong knowledge of cGMP, FDA 21 CFR Part 820, and ISO 13485 regulations., • Hands-on experience with validation protocols, test execution, and statistical analysis., • Proficiency in tools like Minitab, Excel, or other data analysis software., • Excellent technical writing, communication, and organizational skills. Thanks Suchi Company DescriptionVastek Inc is managed by a group of dedicated professionals having rich experience of over years in Healthcare, IT consulting and staffing. We are a certified minority owned, Small business company head quartered out of San Diego, with coverage all across United States, Canada, Mexico, Italy and India. We specialize in Engineering, Validation, Regulatory, IT and NON-IT related areas primarily focused on Pharmaceutical / Life Sciences and Medical device companies.Vastek Inc is managed by a group of dedicated professionals having rich experience of over years in Healthcare, IT consulting and staffing. We are a certified minority owned, Small business company head quartered out of San Diego, with coverage all across United States, Canada, Mexico, Italy and India. We specialize in Engineering, Validation, Regulatory, IT and NON-IT related areas primarily focused on Pharmaceutical / Life Sciences and Medical device companies.

Job DescriptionDescription: ABOUT ELEKTROFI Elektrofi is revolutionizing the delivery of biologic therapies by giving patients the ability to control how they want to receive and benefit from life-changing medicines. Our breakthrough ultra-high concentration microparticle technology platform resolves the limitations associated with intravenously administered biologic therapies by enabling convenient at-home subcutaneous self-administration. With a focus on monoclonal antibodies, therapeutic proteins, and other large molecule drugs, we create, develop, and commercialize subcutaneous biologic therapies in collaboration with strategic partners. We believe a patient-centered healthcare approach can lead to a healthier world. We are headquartered in Boston and innovate globally. We are Formulating the Future of Biologics™. POSITION SUMMARY Elektrofi is seeking a motivated individual to join our biotech company as a Lead Engineer I to support the development of our novel Hypercon™ formulation platform. This individual will drive the technical execution and integration of our platform manufacturing processes across a diverse portfolio of partner development programs. This role is ideal for an experienced engineer who thrives on cross-functional collaboration, technical leadership, and platform standardization. As Lead Engineer I, you will own critical unit operations, guide junior staff, and ensure alignment between platform capabilities and program-specific needs from development through tech transfer. The individual will join a growing, multidisciplinary team of scientists/engineers and industry professionals. KEY RESPONSIBILITIES • Lead the lab execution of development, optimization, and scale-up of platform unit operations (e.g., mixing, TFF, sterile filtration, filling) to support early- and mid-phase clinical programs., • Serve as the technical lead on one or more development programs, ensuring consistency with platform strategy while accommodating partner-specific requirements., • Author and review key development documents (protocols, reports, risk assessments, development history reports) to support CMC regulatory submissions., • Mentor and provide technical oversight to Engineers I–III; promote best practices and continuous improvement within the team., • Collaborate closely with MSAT, QA, Analytical, Formulation, and Regulatory teams to ensure robust and phase-appropriate process design and documentation., • Participate in facility fit assessments, equipment strategy, and technology transfer into GMP environments., • Present technical findings and platform recommendations to internal and external stakeholders., • B.S. in Chemical, Biomedical, Materials, or Pharmaceutical Engineering, or a related engineering discipline w/ 5+ years of relevant experience in biopharmaceutical process development, or M.S. w/ 3+ years of relevant experience., • Strong hands-on experience with bioprocess operations (e.g., TFF, filtration, compounding, mixing, filling)., • Demonstrated ability to lead the lab execution of technical workstreams or cross-functional development projects., • Familiarity with CMC requirements and expectations for clinical-stage programs., • Experience with cGxP and aseptic manufacturing is preferred., • Experience with novel platform development is preferred., • Experience in processes involving ATEX, Class I Div I, Class I Div II equipment design is a plus., • Experience working within a platform development framework supporting multiple external programs., • Experience with single-use systems (SUS), filtration technologies, Downstream DS purification, Drug Product compounding and sterile filtration, and aseptic Fill/Finish. EEOC Statement: Elektrofi provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. To all agencies, please, no phone calls or emails to any employee of Elektrofi about this requisition. All resumes submitted by search firms/employment agencies to any employee at Elektrofi via email, the internet, or in any form and method will be deemed the sole property of Elektrofi unless such search firms/employment agencies were engaged by Elektrofi for this requisition and a valid agreement with Elektrofi is in place. If a candidate submitted outside of the Elektrofi agency engagement process is hired, no fee or payment of any kind will be paid. All candidates must be legally authorized to work in the US. #LI-Onsite

Job DescriptionCompany Description CRB is a leading provider of sustainable engineering, architecture, construction and consulting solutions to the global life sciences and food and beverage industries. Our more than 1,100 employees provide best-in-class solutions that drive success and positive change for our clients, our people and our communities. CRB is a privately held company with a rich history of serving clients throughout the world, consistently striving for the highest standard of technical knowledge, creativity and execution. Job Description We are seeking a skilled and experienced Process Engineer III/ IV with deep expertise in small molecule manufacturing to join our engineering consulting team. This role combines technical leadership with strategic client engagement, supporting process design, scale-up, optimization, and regulatory compliance across a variety of pharmaceutical and chemical industry projects. The Process Engineer III will lead the design and execution of process scopes—such as unit operations, systems, or facility areas—on small to medium-sized projects. You will manage scope, budget, and schedule, while maintaining clear communication with clients and internal teams. This role also includes mentoring junior staff, contributing to high-quality deliverables, and supporting capital project planning and regulatory alignment. This position can be based near any CRB location Key Responsibilities • Lead and support client projects focused on small molecule API process development, scale-up, and manufacturing optimization., • Conduct site assessments, gap analyses, and provide recommendations for process improvements and compliance., • Develop process flow diagrams (PFDs), piping and instrumentation diagrams (P&IDs), and mass/energy balances., • Translate client requirements into actionable design scope and document decisions, open issues, and action items., • Identify and escalate scope changes or design deviations to project leadership., • Collaborate with cross-functional teams including architecture, mechanical, electrical, and construction., • Prepare technical reports, proposals, and presentations for internal and client stakeholders., • Support capital project planning including feasibility studies, equipment selection, and facility design., • Ensure alignment with industry standards including cGMP, FDA, EMA, and ICH guidelines., • Participate in advanced project activities such as:, • Technical bid tabulations, • Vendor package management, • Factory acceptance testing, • Risk assessments (e.g., HAZOP, HACCP), • 3D model reviews and coordination, • Sequence of operations and functional specification reviews, • Mentor junior engineers and design staff., • Lead system design programming and planning with support from senior engineers., • Participate in cross-discipline squad checks and drive overall project quality.Qualifications Minimum Qualifications • Bachelor’s or Master’s degree in Chemical Engineering or a related discipline (ABET-accredited)., • Minimum of 5 years of experience in small molecule process engineering, preferably in a consulting or client-facing role., • Strong understanding of chemical synthesis, purification, and formulation processes., • Experience in design firm or operating company settings within a related industry., • Strong written and verbal communication skills., • Intermediate experience with applicable industry and regulatory guidance and building codes., • Advanced technical knowledge and experience with small molecule API manufacturing equipment and utility systems, such as chemical reactors, filters, centrifuges, dryers, vacuum pumps, scrubbers, purified water, process compressed gases, and engineered heat transfer fluid systems., • Experience designing and implementing engineering controls for containment of highly potent APIs., • EIT or PE certification., • Experience coordinating and managing design within project teams and with external partners., • Familiarity with commissioning, startup, qualification, and troubleshooting of process systems., • Experience with regulatory environments and validation documentation., • Prior experience in engineering consulting or client services., • Familiarity with process safety, risk assessments, and HAZOP studies., • Demonstrated experience leading a small team of process engineers on complex engineering design projects. Additional Information All your information will be kept confidential according to EEO guidelines. CRB is committed to hiring and retaining a diverse workforce. We are proud to be an Equal Opportunity/Affirmative Action Employer and it is our policy to provide equal opportunity to all people without regard to race, color, religion, national origin, ancestry, marital status, veteran status, age, disability, pregnancy, genetic information, citizenship status, sex, sexual orientation, gender identity or any other legally protected category. Employment is contingent on background screening. CRB does not accept unsolicited resumes from search firms or agencies. Any resume submitted to any employee of CRB without a prior written search agreement will be considered unsolicited and the property of CRB. Please, no phone calls or emails. CRB offers a complete and competitive benefit package designed to meet individual and family needs. If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Job DescriptionDescription Verdox is dedicated to reversing climate change through the development and deployment of advanced technology. Our proprietary electro-swing process, developed at MIT, enables carbon dioxide and other acid gasses to be captured with up to 80% less energy and 70% less cost than conventional approaches. We are backed by institutional investors and based in Boston. This is an opportunity to join a dynamic and highly skilled team. Reporting to the Director of Manufacturing, the Lead Process Engineer will lead efforts to develop and commercialize manufacturing processes for our groundbreaking products, and serve as a key contributor to the growth of Verdox. Key Responsibilities • Develop robust roll to roll processes for Verdox proprietary products, including formulation, coating and converting, • Translate prototype designs into scalable solutions achieving performance & cost targets, • Lead formulation production and coating trials at external partners supporting scale up and production of coated electrodes, • Establish in-house capabilities for prototyping and small-scale production, • Establish product and component requirements, ensure quality of incoming materials, • Contribute to strategy development for scale up of production, including capital equipment, supplier selection, make / buy analyses, etc, • Lead process development project teams, • Collaborate with Technology Development and other internal and external stakeholders, • Work with Supply Chain to identify and develop new suppliers, • Create Verdox SOPs related to processes and establish robust best practices Skills Knowledge and ExpertiseEducational background • BS in Chemical Engineering or a relevant engineering discipline, MS preferredWork Experience, • At least 7 years of hands-on experience developing roll to roll processes in coating and converting required, • Experience working in an ISO regulated environment strongly preferred Job Skills, Experience, and Abilities • High level of hands-on experience developing roll to roll processes required, preferably within a structured phase-gate process, • Experience with formulation, coating, laminating, cutting and conversion processes, • Multiple successful projects bringing new products to market at large production scale, • Demonstrated project management experience working with interdisciplinary teams, • Experience specifying and implementing capital equipment projects, • Ability to lead and mentor others, • Ability to thrive in a fast paced, highly collaborative & rapidly evolving startup environment, • Ability to brainstorm and communicate complex technical designs to diverse audiences, • Willingness to contribute in areas outside of core competencies to meet company needs, • Experience with battery products or systems a plus Physical requirements/Work environment • 40% Shop-floor and laboratory work environment, 60% office environment, • Ability to lift components weighing up to 35 lbs. is required, • May be required to sit or stand for prolonged periods, as needed Travel Required • Up to 35-40% possible, including domestic and international sites

Job DescriptionDescription Verdox, Inc. is dedicated to reversing climate change through the development and deployment of advanced technology. The company’s proprietary electro-swing process, developed at MIT, enables carbon dioxide and other acid gasses to be captured with up to 80% less energy and 70% less cost than conventional approaches. Verdox is backed by institutional investors and based in Boston. Verdox seeks a Materials Scientist/Engineer to join our R&D team. This position reports to the Formulation Scientist. Key Responsibilities • Iteratively design, develop and execute novel and scalable formulations guided by materials understanding, structure-property relationships, and functional data, • Build structure/property correlations with functional data and materials properties, to guide innovation, • Develop and execute scalable coating techniques towards the continuous manufacturing of large-area conductive coatings Skills Knowledge and Expertise • Ph.D. in Polymer Science and Engineering, Materials Science and Engineering, Chemistry, Chemical Engineering, with at least 2-5 years of industry experience, • Deep understanding of polymer structure/property relationships and behavior in solution and solid state, • Basic understanding of electrochemistry, electronic and ionically conducting materials is highly desirable, • Proficiency in polymer characterization (solution, solid state) is required, and expertise in characterization of porous materials is highly desirable, • Demonstrated track record of interdisciplinary research, • Strong oral and written communication skills, • Keen attention to detail, • Background in data analysis and statistics strongly desirable, • Comfortable working in an evolutionary and dynamic startup environment

Job DescriptionDescription Verdox, Inc. is dedicated to reversing climate change through the development and deployment of advanced technology. The company’s proprietary electro-swing process, developed at MIT, enables carbon dioxide and other acid gasses to be captured with up to 80% less energy and 70% less cost than conventional approaches. Verdox is backed by institutional investors and based in Boston. Verdox seeks an Electrochemical Engineer to join our R&D team. This position reports to the Chief Technology Officer (CTO). Key Responsibilities • Build and maintain electrochemistry R&D infrastructure, • Comprehensive modeling of electrochemical systems, optimization and sensitivity analysis, charge-rate/capacity optimization, capacitive EDL vs Faradaic electron transfer optimization. Analyze charge transfer, chemical reactions, flow patterns, etc., • Simulation of different operational conditions (charge-rate, gas composition, temperature, pressure) using developed models, • Guide design and fabrication of electrochemical/chemical/mechanical systems – including electrochemical cells, stacking of cells, gas flow channel geometry, etc., • Assist in the development of experimental protocols for testing of electrochemical systems – study of cycle life and calendar life of electrodes and cells; multi-step models to study degradation processes; design of custom-made testing equipment, • Data analysis for performance optimization – prototype to product translation, • PhD in Chemical Engineering, Mechanical Engineering, or equivalent, with a focus on electrochemical systems and energy storage, • Laboratory experience of electrochemical techniques – CV, SWV, G/PITT, RDE, RRDE, CC/CV charge-discharge, EIS, • Advanced quantitative EIS interpretation – equivalent circuit design; data fitting, • Advanced quantitative understanding of electrochemical thermodynamics, kinetics and transport phenomena; interfacial phenomena; porous electrodes; double layer capacitance; charge transfer kinetics (with some quantum chemistry understanding), etc., • Advanced mathematical knowledge (analytical and numerical solutions of PDEs, linear algebra, etc.); Mathematical modeling of complex electrochemical/chemical/mechanical systems, • Some experience in assembly of electrochemical cells (preferred) – fuel cells, flow cells, batteries, capacitors, etc., • Some understanding of organic chemistry and reaction mechanism, • Excel, MATLAB (or equivalent), COMSOL (or equivalent), CAD software, data analysis, DigiElch (or equivalent), EIS simulation., • Ability to work in cross-functional teams, • Strong oral and written communication skills, • Comfortable working in an evolutionary and dynamic startup environment

Location: 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 the global 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 .

Location: Woburn, MA Vaxess is an NIH and venture-funded company developing a pipeline of next-generation therapeutics on the Microneedle Array Patch (MAP) platform. With only five minutes of wear-time on the skin, the self-applied MAP enables sustained delivery in the skin. 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. Device development at Vaxess is cross-disciplinary, integrating mechanical engineering, biomedical engineering, chemical engineering, biomaterials, chemistry, biology, and human factors to address important unmet medical needs. We are seeking a talented, collaborative, and highly motivated engineer with a proven track record in medical device development to support the design of our novel delivery system. Responsibilities • Work under the VP of Device Development to design the re-usable MAP delivery device. Focus for this role will be on product design, development, and design for high volume manufacturability., • Support product development in support of pre-clinical and clinical studies., • Work closely with the multidisciplinary Vaxess team and external consultants with specialties spanning Human Factors, Industrial Design, Packaging, Manufacturing, Engineering, Biocompatibility, Quality, and Regulatory., • Lead the selection and management of outside vendors., • Generate all required documents to support device related components of design control requirements (21 CFR 820, ISO 13485 ISO 14971) and regulatory requirements for combination products (21 CFR Part 4)., • Develop test methods, generate and maintain design specification, write protocols & reports, lead prototype generation, design verifications & validations, conduct FMEA’s, etc. in line with ISO 14971 Risk Management., • Conduct activities within a quality management system following 21CFR820 Quality System Regulation., • Mentor junior team members in the drug-device combination process. Qualifications • BS in Mechanical or Biomedical Engineering, with at least 7 years of direct experience leading the development of medical devices, ideally drug-device combination products., • Understanding of material & test specs generation, protocol & report writing, process & test development, prototyping, design verification, DOE/SPC process optimization & validation (IQ, OQ, PQ), FMEA., • Experience in the development of regulated medical devices or combination products under Design Control (21 CFR 820 / ISO 13485) and ISO 14971 is required., • Ability to read, analyze, and interpret professional journals, technical procedures, and governmental regulations., • Collaborative problem solving, risk assessment, and risk management skills., • Proven time management skills and ability to achieve goals within timelines., • Demonstrated abilities to learn new skills and fields and creatively solve challenging technical problems., • 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. Vaxess aims to recruit, employ, train, compensate and promote regardless of race, religion, color, national origin, sex, gender identity or expression, sexual orientation, disability, age, or veteran status. If you’re interested in joining the Vaxess team, please submit your CV/resume to .

Job Summary – Controls Engineer (Boston/Wilmington, MA) The Controls Engineer will design, program, and implement industrial automation systems. Responsibilities include developing control system architectures, PLC/DCS/HMI-SCADA programming, control panel design, instrumentation, industrial networking, database development, and commissioning. The role may involve project leadership, mentoring, and client interaction. Requirements: • Bachelor’s in Electrical, Controls, Mechanical, Chemical Engineering, or Computer Science, • 5+ years’ experience in automation and controls, • Strong expertise in PLCs (Rockwell Automation), HMI/SCADA (Rockwell, Ignition), DCS (Emerson DeltaV), • Knowledge of automation protocols (Ethernet/IP, Profibus, Modbus, OPC, HART, Foundation Fieldbus), • Familiarity with electrical schematics, NEC standards, SQL databases, • Experience in life sciences industry (cGMP, 21 CFR Part 11, GAMP5, validation) preferred, • Strong leadership and client-facing skills, • Willingness to travel up to 25%

Location: Woburn, MA Vaxess is developing a pipeline of next-generation vaccines and therapeutics on our novel micro-array patch platform. With only five minutes of wear-time on the skin, the self-applied 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. The Senior Mechanical Engineer is a hands-on position involving designing, building, and maintaining automated production equipment throughout its lifecycle. This role will be responsible for design, assembly, installation, qualification, ongoing maintenance, and optimization of automated production systems requiring expert troubleshooting of mechanical assemblies and systems, performing root cause analysis, and implementing corrective actions to ensure efficient, reliable manufacturing operations. Working at Vaxess is cross-disciplinary, integrating chemistry, biology, immunology, mechanical, biomedical, and chemical engineering to address important unmet medical needs. We are seeking a talented, collaborative, and highly motivated individual to join our team. This is a unique opportunity to be part of an emerging startup and significantly influence the strategic growth and future direction of the company as we bring innovative technology to the global vaccine and therapeutic market. Responsibilities • Design, implement, and maintain novel automated systems and solutions that contribute to current manufacturing and scale up of manufacturing operations to eventual commercialization., • Manage external vendors to develop plans, evaluate proposals, and ensure delivery of projects in-scope, within budget, and on time., • Document equipment and procedures though User Requirements Specifications, detailed mechanical, electrical, and assembly drawings, and use and maintenance SOPs. Contribute to the implementation and maintenance of the Quality Management System., • Collaborate closely with cross-functional teams to support product development and manufacturing activities, and to identify and resolve manufacturing issues., • Contribute to continuous improvement to increase safety, quality, and efficiency of manufacturing. Qualifications • BS or advanced degree in Mechanical Engineering or a related discipline., • At least 10 years of experience in designing, building, installing, qualifying, and maintaining automated systems for high volume medical device manufacturing., • Experience writing and executing IQ, OQ and PQ protocols., • Experience developing URS, FAT and SAT documents for automated equipment, • 3D CAD (SolidWorks or similar) as well as Mechanical design of fixtures, assemblies and equipment., • Understanding and working knowledge of mechanical linkages, power transmissions and practices., • Understanding of diverse fabrication techniques, manufacturing processes, and Design for Manufacturability, • 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.

Zaiput Flow Technologies commercializes tools deployed in the context of chemical processing for pharmaceutical applications. Zaiput is passionate about innovation and is committed to achieving excellence through creativity, integrity, teamwork, open communication and prides itself on providing outstanding customer service. We are currently seeking candidates to apply for a full-time Mechanical Development Engineer position to play an important role in the development of a new product line. The ideal candidate will be committed to Zaiput’s mission and values, self-motivated, organized, independent and original in their thinking. Team-work abilities and leadership skills are also essential for this position. Position Description: Zaiput’s current and forthcoming products cover a wide range of applications from laboratory scale to production units. In this context, we are seeking a Mechanical Design Engineer to provide substantial contribution to our product design and R&D efforts. The responsibilities of the job will include participating in brainstorming, design, building and testing to continually improve our current devices, generate prototypes for products under development and launch new products. The work involved in this project is cutting-edge and requires a highly skilled, creative individual possessing strong applied design capabilities. While the products will be the result of teamwork, because of the required multidisciplinary approach, the mechanical engineer will have a key role in the design of the mechanical and fluidic components of the systems. Importantly, the multidisciplinary nature of Zaiput’s work requires the teams to keep tight internal interaction and have excellent communication. The variety of responsibilities and broadness of the tasks makes this position an exciting professional opportunity for a very motivated, driven engineer. This is a unique opportunity to join a project and experience the exciting journey from conception to commercialization. More information about the projects will be provided to interested candidates. Responsibilities include: -\tDesigning and testing components and subassemblies for current and future product lines -\tGenerating 2D and 3D design packages to internal drawing standards -\tGenerating and maintaining Bill of Materials for multiple products -\tGathering quotes for components and managing suppliers to source development materials. -\tParticipating in engineering design reviews -\tTriaging field issues and converting those issues into product changes -\tPrototyping fixes and features using on-site machine shop and tools -\tGenerating documentation for engineering verification, SOP’s, and concept development -\tNurturing a product line from concept to production release Desired skills and experience: -\tBSME or MSME from accredited university -\t4-5 years of experience in engineering design, preferably in a smaller team environment. -\tExcellent knowledge of the fundamentals of engineering -\tDemonstrated ability to troubleshoot of mechanical and electrical systems. •\tFlexibility in undertaking and participating in different tasks and activities. -\tDemonstrated eagerness to learn and grow in a collaborative team environment. -\tDemonstrated ability to work in a cross-functional manner. -\tExcellent technical writing skills -\tExcellent communication and interpersonal skills with the ability to understand and present technical details. -\tExcellent task management and prioritization skills. -\tProficiency in SolidWorks, Labview, Arduino -\tAt least some knowledge of PLC programming and troubleshooting is required. -\tAbility to travel on occasions internationally to assist on customer installs -\tExperience programming CNC milling centers is a valuable plus -\tExperience in a manufacturing setting is a valuable plus -\tExperience in Solidworks PDM, is a valuable plus Employment: This is a full-time position on site; the compensation package depends on qualifications and includes full benefits. To apply: Please send a CV/resume to Matt Ewing at . If you would like to get to the top of the list, please provide the following writing exercise: """ Prompt: Describe one solo project (non-team work) which showcases your hands-on fabrication abilities, creativity, and deep knowledge of something. Format: Provide a single (1) page PDF of technical writing, with pictures**. No specific formatting required, but put an effort into making it look nice on the page. **Please ensure that all pictures and descriptions are limited to non-proprietary information. """ About Zaiput Flow Technologies Zaiput Flow Technologies commercializes groundbreaking proprietary technology that enables continuous liquid-liquid/gas-liquid separation for chemical manufacturing as well as new reactor technology for continuous hydrogenation and new crystallization technology for continuous crystallization. Zaiput’s technology and products are used mostly in for pharmaceutical and fine chemicals production. Zaiput is committed to the development and commercialization of new, high quality tools for the enhancement and growth of flow chemistry and chemical manufacturing technology. As an MIT spinoff, innovative R&D is at its core as well as strong professional and ethical values.

General Overview Emvolon Inc. () is an innovative MIT spin-off on a mission to convert greenhouse gas emissions into carbon-negative fuels and chemicals like green methanol and green ammonia. Leveraging our patented technology, we transform car engines into cost-effective, modular chemical plants. This groundbreaking approach enables us to support various industries, including maritime, aviation, energy, waste management and agriculture, in powering the global economy without emissions. At Emvolon, we are proud to have attracted capital from notable VC funds and have been recognized with grants from ARPA-E, the US Department of Energy, the US Department of Agriculture, and the National Science Foundation. Job Summary We are seeking an experienced and highly driven Senior Process Engineer with a strong background in EPC project execution and proven history of developing FEED packages for chemicals/fuels and novel process scale-up, to lead the development and execution of our first-of-a-kind (FOAK) gas-to-methanol conversion technology. This position offers a unique opportunity to play a pivotal role in commissioning of a transformative, cost-effective chemicals production technology. In this role you will lead key engineering efforts across FEED, detailed design, fabrication, and start-up, partnering closely with EPC contractors, technology partners, and internal R&D teams. This role is ideal for an experienced process engineer who is eager to apply EPC discipline to emerging clean technologies, and help scale innovative gas-to-chemicals solutions to commercial reality. Role Responsibilities • Lead engineering efforts for FOAK systems from engineering design through commissioning, ensuring delivery of safe, robust, and scalable process design, • Provide technical leadership on core process engineering deliverables such as Process Flow Diagrams (PFDs), Piping and Instrumentation Diagrams (P&IDs), Heat and Material Balances and Equipment datasheets and specifications, • Execute and validate process simulations using Aspen HYSYS to support equipment sizing and system optimization, • Drive and support FEED and detailed engineering in collaboration with EPC firms, ensuring alignment with project schedules, cost targets, and regulatory requirement, • Support HAZOPs, PHAs, and other process safety reviews, integrating best practices into engineering design and operation plans, • Oversee the design, procurement, and integration of modular/skid-mounted process systems, ensuring fit-for-purpose design and manufacturability, • Provide hands-on technical support during FAT, commissioning, and start-up of pilot and demonstration systems, including on-site troubleshooting and optimization, • Assist development of standard operating procedures (SOPs), control philosophies, and start-up guides to ensure safe and consistent plant operation, • Work cross-functionally with R&D, operations, and business development teams to meet technical milestones and customer-driven performance metrics, • Champion a strong safety culture, ensuring compliance with EH&S standards and applicable codes (e.g., API, ASME, NFPA) Required Qualifications • Master’s or Bachelor’s degree in Chemical Engineering or related field., • 7+ years of process engineering experience in EPC project environments, including FEED, detailed design, and start-up, • Proven experience in process scale-up, especially in novel or first-of-a-kind technologies, and working with modular or skid-mounted systems, • Deep understanding of gas processing, hydrocarbon separation, and reactor-based systems (preferably methanol synthesis or syngas conversion), • Demonstrated ability to translate process requirements into industrial-grade engineering packages and work effectively with multidisciplinary EPC teams, • Strong hands-on experience with process simulation tools (e.g., Aspen HYSYS), • Field experience with plant commissioning, troubleshooting, and start-up, • Knowledge of process automation, instrumentation, and control systems is a plus., • Strong understanding of process safety, with experience conducting and implementing HAZOP recommendations Preferred Attributes • Experience in early-stage clean tech, startups, or FOAK commercialization environments, • Knowledge of renewable natural gas (RNG), syngas processing, or alternative fuels, • Excellent communication skills and the ability to coordinate effectively with diverse stakeholders including EPC contractors, vendors, and internal teams, • High tolerance for ambiguity, with a hands-on, problem-solving mindset and ability to thrive in fast-paced development environments, • Willingness to travel to field sites and fabrication yards during critical phases of project execution Location, Travel & Work Authorization • This is a full-time, on-site role based at our Woburn, MA facility. We are seeking candidates who can work in person as part of a highly collaborative, hands-on engineering team. While the role is primarily office and lab-based, periodic travel is expected to support commissioning and troubleshooting activities at partner and pilot plant sites., • Applicants must be currently authorized to work in the United States for any employer. We are unable to sponsor or take over sponsorship of employment visas at this time. Benefits • Health and dental insurance for employees and dependents, • Generous time off and unplugged time, • Flexible work hours and hybrid work opportunities, • Professional development and continuous learning At Emvolon, our MIT roots run deep in innovation and rigorous scientific and entrepreneurial pursuits. We champion collaboration, a growth mindset, accountability, and diverse perspectives, all while prioritizing employee support and a flexible work environment. Emvolon is proud to be an equal opportunity employer. All qualified 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 characteristic protected by the law. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification document form upon hire Please submit your application to

Device development at Vaxess is cross-disciplinary, integrating mechanical engineering, biomedical engineering, chemical engineering, biomaterials, chemistry, biology, and human factors to address important unmet medical needs. We are seeking a talented, collaborative, and highly motivated engineer

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