<h1><strong>Job Title: <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">Senior</span></span></span></span> Mechanical Engineer</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a talented Mechanical Engineer to lead HVAC system designs, including ductwork, piping, and controls across diverse projects. The role involves performing load calculations to ensure system efficiency and compliance, overseeing multiple projects from concept to completion, and managing a team of engineers. This position requires collaboration with architects and contractors to integrate HVAC solutions into building designs, participation in business development efforts, and ensuring regulatory compliance. The ideal candidate will utilize AutoCAD, Revit, and HVAC modeling software to develop system layouts and specifications.</p><p><br></p><h2>Responsibilities</h2><ul><li>Lead the design of HVAC systems, including ductwork, piping, and controls.</li><li>Perform heating and cooling load calculations for system efficiency.</li><li>Oversee projects from concept to completion, ensuring adherence to budgets and timelines.</li><li>Manage and mentor a team of 6-7 engineers, providing technical guidance and professional development.</li><li>Conduct site visits and inspections as needed.</li><li>Be involved in Fire Protection and Plumbing design.</li><li>Participate in business development efforts, including client meetings and proposal development.</li><li>Ensure designs meet building codes, ASHRAE standards, and energy regulations.</li><li>Collaborate with architects, contractors, and other engineering disciplines.</li><li>Utilize AutoCAD, Revit, and HVAC modeling software for design.</li></ul><h2>Essential Skills</h2><ul><li>Proven management experience for a team of up to 7 engineers.</li><li>Ability to design all aspects of HVAC systems including cooling plants, chillers, and heating plants.</li><li>Proficiency in AutoCAD and Trane Trace.</li><li>Strong communication and negotiation skills.</li><li>Bachelor’s or Master’s degree in Mechanical Engineering.</li><li>10+ years of experience in HVAC design, including leadership roles.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Professional Engineer (PE) license preferred.</li><li>Experience in mechanical design, plumbing, fire protection, and MEP design.</li><li>Willingness to travel to job sites as needed.</li></ul><h2>Work Environment</h2><p>This position is based in Northern NJ, with in-office work required five days a week. The firm fosters a casual environment, encouraging professional development and continuous career growth. Flexible start times are offered between 7am and 9am. The work environment promotes efficiency with all architects and engineering trades in-house, allowing for seamless project execution. The team works on a variety of public and private projects, ranging from small to large in scope, ensuring every project is unique and interesting.</p>

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Senior Mechanical Engineer

<h1><strong>Job Description: Sr. Mechanical Engineer</strong></h1><p>We are seeking a Sr. Mechanical Engineer to lead and manage complex mechanical design projects for custom packaging machinery and systems. This role demands technical expertise in mechanical design, CAD, troubleshooting, and risk assessments, along with the ability to support cross-functional teams and drive continuous improvement in design and manufacturing processes. The ideal candidate will also be responsible for documentation, design reports, and manual writing.</p><p><br></p><h2>Responsibilities</h2><ul><li>Lead detailed mechanical design projects for custom packaging machinery and systems.</li><li>Provide technical support to the sales team in developing layout drawings and high-level quotes that meet engineering specifications.</li><li>Collaborate with manufacturing teams to ensure designs are feasible and aligned with production capabilities; assist in selecting materials and processes.</li><li>Offer technical guidance to aftermarket, service, and installation technicians, with potential for on-site support.</li><li>Implement best practices for design for assembly, ensuring machinery is easy to assemble and maintain.</li><li>Prepare and maintain engineering documentation, including specifications, design reports, and user manuals.</li><li>Create mathematically verified concepts to resolve packaging challenges, including material analysis, stress/strain, vibration, and pneumatic expectations.</li><li>Evaluate and select components that meet the technical and physical constraints outlined in project scopes.</li><li>Design within safety constraints and conduct design risk assessments for verification and documentation.</li><li>Design new or specialized integrations/modifications according to established specifications regarding size, capacities, and performance.</li><li>Collaborate with engineering teams, project management, and key stakeholders to address and resolve manufacturing, design, and quality issues, ensuring continuous improvement of processes and methods.</li><li>Lead design optimization projects to enhance overall design.</li></ul><h2>Essential Skills</h2><ul><li>High-level engineering aptitude.</li><li>Experience in mechanical design.</li><li>Proficiency in CAD software such as Autodesk Inventor.</li><li>Ability to conduct troubleshooting and root cause analysis.</li><li>Knowledge of mechanical components, pneumatics, GD&amp;T, conveyor systems, hydraulic systems, and sensor technology.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s degree in mechanical engineering or related field with 7+ years of experience; a master’s degree is a plus.</li><li>Experience with manufacturing processes, industry standards, and regulations in packaging machinery.</li><li>Familiarity with sanitary design concepts for food production and packaging machines is preferred.</li><li>Experience in pneumatic system design is a plus.</li></ul>

<p><strong>Description</strong></p><p>We are seeking an experienced Estimator with 10+ years of estimating experience, including 5 years as a <span style="background-color: none; color: rgb(8, 7, 7);">Sr</span> Estimator and 5 years as a Project Manager concurrently with their estimating responsibilities. This role requires expertise in preparing accurate cost estimates, analyzing project specifications, and managing bidding processes while overseeing project execution to ensure budget and timeline alignment. The estimator would be someone who has been working with a reputable General Contractor for at least 5-10 years as a mid to <span style="background-color: none; color: rgb(8, 7, 7);">sr</span> level estimator with project management experience. It is a big plus if they have experience with estimating mechanical.</p><p><br></p><p><strong>Skills</strong></p><p>Project management, Construction, Estimation, mechanical estimator, Bidding, Construction management, Estimating software</p><p><br></p><p><strong>Additional Skills &amp; Qualifications</strong></p><p>10+ years of estimating experience, with at least 5 years in a <span style="background-color: none; color: rgb(8, 7, 7);">sr </span>estimator role.</p><p>5+ years of project management experience, concurrently with estimating responsibilities.</p><p>Strong knowledge of construction methodologies, materials, and cost structures.</p><p>Proficiency in estimating software and project management tools.</p><p>Excellent analytical, communication, and negotiation skills.</p><p>Ability to work in a fast-paced environment and manage multiple projects simultaneously.</p>

Senior Mechanical Estimator

<p><strong>Actalent Honolulu is seeking a skilled and experienced <span style="color: rgb(8, 7, 7); background-color: none;">Senior</span> Planner to lead complex environmental and land use planning projects across Hawai‘i.</strong></p><p><br></p><p>The <span style="color: rgb(8, 7, 7); background-color: none;">Senior</span> Planner leads the technical aspects of environmental and land use planning and permitting projects. This role requires advanced planning expertise, team oversight, and collaboration with clients, public officials, and community stakeholders to ensure successful, timely, and budget-conscious project delivery. The ideal candidate is a creative problem-solver with strong leadership and communication skills.</p><p><br></p><p><strong>Project Management:</strong></p><ul><li>Coordinate technical aspects of projects from start to finish.</li><li>Oversee office staff and subconsultants.</li><li>Monitor schedules, budgets, and project risks.</li></ul><p><strong>Planning &amp; Development:</strong></p><ul><li>Conduct research, fieldwork, and regulatory assessments.</li><li>Prepare environmental assessments, land use plans, and permit applications.</li><li>Advise on land use and environmental policy.</li><li>Lead public consultations and stakeholder engagement.</li><li>Monitor trends in regulations and sustainability.</li></ul><p><strong>Leadership:</strong></p><ul><li>Supervise planners, interns, and support staff.</li><li>Provide technical guidance and promote team development.</li><li>Set goals and evaluate performance.</li><li>Foster a positive, service-oriented culture.</li></ul><p><strong>Client &amp; Stakeholder Relations:</strong></p><ul><li>Coordinate with clients, agencies, and contractors.</li><li>Build strong relationships and support business development.</li></ul><p><strong>Quality &amp; Safety:</strong></p><ul><li>Ensure technical quality and regulatory compliance.</li><li>Address safety concerns and uphold industry standards.</li></ul><p><strong>Documentation:</strong></p><ul><li>Maintain accurate and up-to-date project records.</li></ul><p><strong>Qualifications:</strong></p><ul><li>Bachelor’s or Master’s in planning, geography, environmental science, or related field.</li><li>AICP certification preferred.</li><li>8+ years of experience in environmental and land use planning.</li><li>Strong leadership, communication, and project implementation skills.</li><li>Proficient in GIS, Microsoft Office, and project management tools.</li></ul><h4><em>This is a condensed job description. A more in-depth description will be shared after further screening.</em></h4>

Senior Planner (Environmental/Land Use)

<h3><span style="color: rgb(8, 7, 7); background-color: none;">Senior</span> Platform Engineer</h3><p>Location:Aurora, CO (Onsite)</p><p>Start Date:Contingent upon project award (Estimated July 2025)</p><p>Clearance Required:Active TS/SCI with CI Poly (U.S. Citizenship required)</p><p><br></p><p>As a <span style="color: rgb(8, 7, 7); background-color: none;">Senior</span> Platform Engineer, you’ll be at the forefront of a transformative era in software engineering — one that blends development and operations into a unified, high-impact platform. You’ll empower development teams by streamlining processes, enhancing collaboration, and accelerating release cycles.</p><p>You’ll work on a team managing hybrid-cloud environments that support the development and testing of a critical national asset. This includes hands-on engineering, documentation, and baseline control.</p><p><br></p><h3>What You’ll Do</h3><ul><li>Support the transition of tightly coupled systems to modern infrastructure</li><li>Design, develop, and support CI/CD pipelines across on-prem cloud environments</li><li>Automate configuration management and improve infrastructure efficiency</li><li>Collaborate with software engineers, data scientists, and DevOps teams</li><li>Integrate security and compliance services (e.g., encryption, access management)</li><li>Provide operational support for platform environments</li><li>Work with technologies like Red Hat Linux (v7+, 8+), Rancher, Docker, Kubernetes</li></ul><h3>Basic Qualifications</h3><ul><li>Bachelor’s degree in STEM (Computer Science, Engineering, IT, or Physics) + 5 years of experience</li><li>Experience with automation tools (Chef, Puppet, Ansible)</li><li>Skilled in COTS/FOSS product integration</li><li>Proficient with containerization and orchestration (Docker, Podman, Kubernetes, Rancher)</li><li>Active TS/SCI with CI Poly clearance (required on Day 1)</li></ul><h3>Preferred Qualifications</h3><ul><li>Experience with CI/CD tools (Jira, Confluence, Bitbucket, Jenkins, GitLab, Artifactory)</li><li>Exposure to AWS or other cloud services</li><li>Knowledge of secure coding practices (OWASP, secrets management)</li><li>Familiarity with networking, scanning tools (Nessus, Fortify, Anchore)</li><li>Multi-disciplinary infrastructure experience (compute, storage, virtualization)</li><li>Programming/scripting skills (Python, Java, Bash, Perl, Ruby, C++)</li><li>DoD 8570 certification (e.g., Security+, CCNA) or ability to obtain</li></ul>

Senior Platform DevOps Engineer

<h1 style="text-align: center;"><strong>Full-Time <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">Senior</span></span></span> Product Engineer</strong></h1><p><br></p><h2>Job Description</h2><p>The <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">Senior</span></span></span> Product Engineer leads initiatives across the full product lifecycle, from conception through commercialization and sustaining. This hands-on role requires expertise in mechanical design, system integration, prototype fabrication and testing, and process development. The ideal candidate will thrive in diverse work environments, possess strong management and leadership skills, and have a deep understanding of product engineering principles to drive innovation and maintain product excellence.</p><p><br></p><h2>Responsibilities</h2><ul><li>Analyze and optimize designs for functionality, reliability, and manufacturability using computer-aided analysis and classical engineering techniques.</li><li>Plan, evaluate, and execute activities related to new product concepts, design changes, and product improvements.</li><li>Lead and collaborate with cross-functional teams to manage all stages of product development and engineering changes.</li><li>Translate customer needs and specifications into detailed mechanical designs.</li><li>Develop and implement systems and processes to enhance product quality and customer value.</li><li>Manage projects to ensure timely delivery, budget compliance, and return on investment.</li><li>Provide technical leadership and mentorship to junior engineers.</li><li>Prepare, review, and communicate Engineering Change Requests or Temporary Design Deviations to stakeholders.</li><li>Conduct informal and formal design reviews, as well as design verification and validation testing.</li><li>Investigate quality deviations to determine root causes and implement corrective actions.</li><li>Evaluate non-conformances or field failures and implement corrective actions or design improvements.</li><li>Support the regulatory team with medical device registrations by providing engineering expertise.</li><li>Manage product costing and maintain Bills of Materials within the document management system.</li><li>Assist internal and external teams in troubleshooting technical issues.</li><li>Adhere to safety protocols and company policies at all times.</li></ul><h2>Essential Skills</h2><ul><li>A minimum of 7 years’ experience in product development in a regulated industry such as medical device, pharmaceutical, aerospace, or automobile.</li><li>Bachelor’s Degree or higher in Mechanical Engineering, Biomechanical Engineering or equivalent related disciplines.</li><li>Expertise in design control, GD&amp;T, geometric dimensioning, geometric tolerancing, and design for manufacturability.</li><li>Proven experience with design verification, validation, and FMEA.</li><li>Proficiency with CAD tools such as SolidWorks and statistical analysis tools including Minitab, ANOVA, and DOE.</li><li>Knowledge of regulatory standards including ISO, EU MDR, and FDA GMP.</li><li>Strong communication skills to convey technical concepts to non-technical stakeholders.</li><li>Ability to lead and collaborate effectively within cross-functional teams.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with problem-solving methodologies such as PDCA, 5 Why&#39;s, and Ishikawa analysis.</li><li>Experience with Engineering Change Orders, New Product Development processes, and Design Transfer.</li><li>Proven ability to manage projects and deliver results in a dynamic environment.</li><li>Commitment to continuous learning and professional development.</li><li>Ability to travel as required.</li></ul>

Senior Product Engineer

<h1 style="text-align: center;"><strong>Full-Time <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">Senior</span></span> Product Engineer</strong></h1><p><br></p><h2>Job Description</h2><p>The <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">Senior</span></span> Product Engineer leads initiatives across the full product lifecycle, from conception through commercialization and sustaining. This hands-on role requires expertise in mechanical design, system integration, prototype fabrication and testing, and process development. The ideal candidate will thrive in diverse work environments, possess strong management and leadership skills, and have a deep understanding of product engineering principles to drive innovation and maintain product excellence.</p><p><br></p><h2>Responsibilities</h2><ul><li>Analyze and optimize designs for functionality, reliability, and manufacturability using computer-aided analysis and classical engineering techniques.</li><li>Plan, evaluate, and execute activities related to new product concepts, design changes, and product improvements.</li><li>Lead and collaborate with cross-functional teams to manage all stages of product development and engineering changes.</li><li>Translate customer needs and specifications into detailed mechanical designs.</li><li>Develop and implement systems and processes to enhance product quality and customer value.</li><li>Manage projects to ensure timely delivery, budget compliance, and return on investment.</li><li>Provide technical leadership and mentorship to junior engineers.</li><li>Prepare, review, and communicate Engineering Change Requests or Temporary Design Deviations to stakeholders.</li><li>Conduct informal and formal design reviews, as well as design verification and validation testing.</li><li>Investigate quality deviations to determine root causes and implement corrective actions.</li><li>Evaluate non-conformances or field failures and implement corrective actions or design improvements.</li><li>Support the regulatory team with medical device registrations by providing engineering expertise.</li><li>Manage product costing and maintain Bills of Materials within the document management system.</li><li>Assist internal and external teams in troubleshooting technical issues.</li><li>Adhere to safety protocols and company policies at all times.</li></ul><h2>Essential Skills</h2><ul><li>A minimum of 7 years’ experience in product development in a regulated industry such as medical device, pharmaceutical, aerospace, or automobile.</li><li>Bachelor’s Degree or higher in Mechanical Engineering, Biomechanical Engineering or equivalent related disciplines.</li><li>Expertise in design control, GD&amp;T, geometric dimensioning, geometric tolerancing, and design for manufacturability.</li><li>Proven experience with design verification, validation, and FMEA.</li><li>Proficiency with CAD tools such as SolidWorks and statistical analysis tools including Minitab, ANOVA, and DOE.</li><li>Knowledge of regulatory standards including ISO, EU MDR, and FDA GMP.</li><li>Strong communication skills to convey technical concepts to non-technical stakeholders.</li><li>Ability to lead and collaborate effectively within cross-functional teams.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with problem-solving methodologies such as PDCA, 5 Why&#39;s, and Ishikawa analysis.</li><li>Experience with Engineering Change Orders, New Product Development processes, and Design Transfer.</li><li>Proven ability to manage projects and deliver results in a dynamic environment.</li><li>Commitment to continuous learning and professional development.</li><li>Ability to travel as required.</li></ul>

<h1 style="text-align: center;"><strong>Full-Time <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">Senior</span></span></span></span> Product Engineer</strong></h1><p><br></p><h2>Job Description</h2><p>The <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">Senior</span></span></span></span> Product Engineer leads initiatives across the full product lifecycle, from conception through commercialization and sustaining. This hands-on role requires expertise in mechanical design, system integration, prototype fabrication and testing, and process development. The ideal candidate will thrive in diverse work environments, possess strong management and leadership skills, and have a deep understanding of product engineering principles to drive innovation and maintain product excellence.</p><p><br></p><h2>Responsibilities</h2><ul><li>Analyze and optimize designs for functionality, reliability, and manufacturability using computer-aided analysis and classical engineering techniques.</li><li>Plan, evaluate, and execute activities related to new product concepts, design changes, and product improvements.</li><li>Lead and collaborate with cross-functional teams to manage all stages of product development and engineering changes.</li><li>Translate customer needs and specifications into detailed mechanical designs.</li><li>Develop and implement systems and processes to enhance product quality and customer value.</li><li>Manage projects to ensure timely delivery, budget compliance, and return on investment.</li><li>Provide technical leadership and mentorship to junior engineers.</li><li>Prepare, review, and communicate Engineering Change Requests or Temporary Design Deviations to stakeholders.</li><li>Conduct informal and formal design reviews, as well as design verification and validation testing.</li><li>Investigate quality deviations to determine root causes and implement corrective actions.</li><li>Evaluate non-conformances or field failures and implement corrective actions or design improvements.</li><li>Support the regulatory team with medical device registrations by providing engineering expertise.</li><li>Manage product costing and maintain Bills of Materials within the document management system.</li><li>Assist internal and external teams in troubleshooting technical issues.</li><li>Adhere to safety protocols and company policies at all times.</li></ul><h2>Essential Skills</h2><ul><li>A minimum of 7 years’ experience in product development in a regulated industry such as medical device, pharmaceutical, aerospace, or automobile.</li><li>Bachelor’s Degree or higher in Mechanical Engineering, Biomechanical Engineering or equivalent related disciplines.</li><li>Expertise in design control, GD&amp;T, geometric dimensioning, geometric tolerancing, and design for manufacturability.</li><li>Proven experience with design verification, validation, and FMEA.</li><li>Proficiency with CAD tools such as SolidWorks and statistical analysis tools including Minitab, ANOVA, and DOE.</li><li>Knowledge of regulatory standards including ISO, EU MDR, and FDA GMP.</li><li>Strong communication skills to convey technical concepts to non-technical stakeholders.</li><li>Ability to lead and collaborate effectively within cross-functional teams.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with problem-solving methodologies such as PDCA, 5 Why&#39;s, and Ishikawa analysis.</li><li>Experience with Engineering Change Orders, New Product Development processes, and Design Transfer.</li><li>Proven ability to manage projects and deliver results in a dynamic environment.</li><li>Commitment to continuous learning and professional development.</li><li>Ability to travel as required.</li></ul>

<h1><strong>Director of Program Manager</strong></h1><p>The Director, Program Management - SAP S4HANA will lead the global transformation from SAP ECC6 to S/4HANA, ensuring a seamless transition across operations, manufacturing, supply chain, IT, and finance. This role is accountable for driving the end-to-end program lifecycle—from strategy and planning through execution and delivery—while aligning stakeholders, managing risks, and maintaining transparency at all levels.</p><p><br></p><h2>Responsibilities</h2><ul><li>Lead project scoping, planning, and execution in alignment with business goals and the transformation roadmap.</li><li>Drive integration of internal and external elements across global functions.</li><li>Oversee business process reengineering efforts to align with the S/4HANA platform.</li><li>Establish and enforce program governance, including decision-making frameworks, clear roles, and escalation paths.</li><li>Ensure effective communication and engagement across executive leadership, the steering committee, and stakeholders.</li><li>Create and execute communication strategies that effectively convey the vision for change and maintain engagement throughout the transformation.</li><li>Manage project timelines, ensuring milestones are met within defined timeframes.</li><li>Build and maintain strong relationships with key stakeholders.</li></ul><h2>Essential Skills</h2><ul><li>Successful leadership of full lifecycle implementation of SAP S/4HANA from SAP ECC6 in a global, highly regulated environment.</li><li>Proven experience delivering large-scale, cross-functional ERP programs with discipline, urgency, and a focus on measurable business value.</li><li>Minimum 10 years SAP implementation experience.</li><li>Minimum of 5 years experience in the medical device/biomedical industry or regulatory environment.</li><li>Experience in developing and implementing change management strategies globally.</li><li>Proficiency in working with SAFE Agile teams.</li><li>Executive level communication and presentation skills.</li><li>Understanding of LEAN principles and experience in applying such principles.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s degree in a technical or business discipline or equivalent education and experience.</li><li>MBA preferred.</li><li>PMP or equivalent certification preferred.</li><li>Skills in cost estimation, budget management, and cost-benefit analysis.</li><li>Strong problem-solving abilities and capability to analyze complex data.</li><li>Exceptional verbal and written communication skills to articulate project and program objectives to internal and external teams.</li></ul><h2>Work Environment</h2><p>The work environment involves leading a transformative program in a global, highly regulated setting. The position requires collaboration with cross-functional teams and engagement with executive leadership. The role entails managing complex program execution and operational excellence, utilizing technologies and methodologies such as SAP S/4HANA, SAFE Agile, and LEAN principles.</p>

Senior Program Manager

<h1 style="font-weight: 700;">Job Title: <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">Senior</span></span> Project Manager</h1><br><h2>Job Description</h2><p>This position is for a Director of Programs role located in the Saint Louis area, tasked with leading programs for the Heavy Systems Manufacturing line of business. The role involves full life cycle management, including development, production, and sustainment of the business segment.</p><br><h2>Responsibilities</h2><ul><li>Lead programs for the Heavy Systems Manufacturing line of business.</li><li>Manage full life cycle of projects including development, production, and sustainment.</li><li>Oversee multi-million dollar project budgets with strong understanding of government contracts.</li><li>Coordinate with key stakeholders across supply chain, operations, manufacturing, engineering, and legal departments.</li><li>Work within the defense industry, ensuring projects meet required deadlines.</li><li>Touch on &#39;seedling&#39; lines of business that are currently in development, adapting to evolving program requirements.</li></ul><h2>Essential Skills</h2><ul><li>Expertise in project and program management, particularly within a defense contract manufacturer.</li><li>Strong knowledge of manufacturing operations and government contract structures.</li><li>Proficiency in Microsoft program management tools such as Teams and Project.</li><li>PMP certification.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor&#39;s degree in engineering or business.</li><li>9+ years of experience in program management.</li></ul><h2>Work Environment</h2><p>The role is based west of St. Louis International Airport in a modern facility. This position involves interaction with primary customers, the Army and Air Force, and includes travel to the West Plaines manufacturing facility a couple of times a month. This is a hybrid role with remote work on Mondays and Fridays, and in-office presence on Tuesdays, Wednesdays, and Thursdays. The organization follows a schedule allowing every other Friday off.</p><br>

<h1><strong>Job Title: Director of Program Manager</strong></h1><p><br></p><h2>Job Description</h2><p>The Director, Program Management - SAP S4HANA will lead the global transformation from SAP ECC6 to S/4HANA, ensuring a seamless transition across operations, manufacturing, supply chain, IT, and finance. This role is accountable for driving the end-to-end program lifecycle—from strategy and planning through execution and delivery—while aligning stakeholders, managing risks, and maintaining transparency at all levels.</p><p><br></p><h2>Responsibilities</h2><ul><li>Lead project scoping, planning, and execution in alignment with business goals and the transformation roadmap.</li><li>Drive integration of internal and external elements across global functions.</li><li>Oversee business process reengineering efforts to align with the S/4HANA platform.</li><li>Establish and enforce program governance, including decision-making frameworks, clear roles, and escalation paths.</li><li>Ensure effective communication and engagement across executive leadership, the steering committee, and stakeholders.</li><li>Create and execute communication strategies that effectively convey the vision for change and maintain engagement throughout the transformation.</li><li>Manage project timelines, ensuring milestones are met within defined timeframes.</li><li>Build and maintain strong relationships with key stakeholders.</li></ul><h2>Essential Skills</h2><ul><li>Successful leadership of full lifecycle implementation of SAP S/4HANA from SAP ECC6 in a global, highly regulated environment.</li><li>Proven experience delivering large-scale, cross-functional ERP programs with discipline, urgency, and a focus on measurable business value.</li><li>Minimum 10 years SAP implementation experience.</li><li>Minimum of 5 years experience in the medical device/biomedical industry or regulatory environment.</li><li>Experience in developing and implementing change management strategies globally.</li><li>Proficiency in working with SAFE Agile teams.</li><li>Executive level communication and presentation skills.</li><li>Understanding of LEAN principles and experience in applying such principles.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s degree in a technical or business discipline or equivalent education and experience.</li><li>MBA preferred.</li><li>PMP or equivalent certification preferred.</li><li>Skills in cost estimation, budget management, and cost-benefit analysis.</li><li>Strong problem-solving abilities and capability to analyze complex data.</li><li>Exceptional verbal and written communication skills to articulate project and program objectives to internal and external teams.</li></ul><h2>Work Environment</h2><p>The work environment involves leading a transformative program in a global, highly regulated setting. The position requires collaboration with cross-functional teams and engagement with executive leadership. The role entails managing complex program execution and operational excellence, utilizing technologies and methodologies such as SAP S/4HANA, SAFE Agile, and LEAN principles.</p>

<h1><em><u>APPLY NOW! </u></em></h1><h1><strong>Hiring SR. Project Manager!! </strong></h1><p><strong><em><u>FOR IMMEDIATE CONSIDERATION EMAIL: msemmel@actalentservices.com!!</u></em></strong></p><h2><br></h2><h2>Job Description</h2><p>We are seeking a dedicated SR. Project Manager to lead and manage construction projects, ensuring successful contract reviews, scope of work management, and the cultivation and selection of subcontractors. This role involves running various meetings, enforcing policies on job sites, and mentoring assistant project managers.</p><p><br></p><h2>Responsibilities</h2><ul><li>Conduct thorough contract reviews.</li><li>Manage and oversee the scope of work for each project.</li><li>Cultivate, review, and select subcontractors for each project.</li><li>Run internal and external meetings, including foreman and municipal meetings.</li><li>Enforce company policies on job sites.</li><li>Mentor and direct assistant project managers.</li></ul><h2>Essential Skills</h2><ul><li>Bachelor&#39;s degree or higher in a related field or equivalent experience.</li><li>10+ years of project management experience with projects over $5 million.</li><li>Proficiency in Procore software.</li><li>Strong skills in document control, design, and estimation.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with joint venture billing.</li><li>Experience managing projects over $15 million.</li></ul><h2>Work Environment</h2><p>This role requires working on project sites or in the office, specifically for school projects, which necessitates on-site presence for the next 2+ years in Bristol, CT. The company boasts a strong employee retention rate with an average tenure of 15 years. The company culture includes an open-door policy with owners accessible and involved in projects. Benefits include a fully insured take-home vehicle. Our projects are diverse and stable, with a strong track record in the market. The project team comprises 50 employees, split between office and labor, with two superintendents on site working alongside the <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">Senior</span></span> Project Manager.</p>

Senior Project Manager

<h1><strong>Sr. Project Manager</strong></h1><p><br></p><h2>Job Description</h2><p>The Sr. Project Manager will oversee multiple current and upcoming projects at Dulles Airport, including bathroom upgrades, new baggage claim facilities, and terminal upgrades. This role involves overseeing permitting, change orders, and updates, as well as running meetings with clients to discuss project progress. Collaboration with internal and client teams is essential for developing schedules, daily logs, and reports. The candidate will manage construction, design, procurement, schedule, and financial aspects of the projects.</p><p><br></p><h2>Responsibilities</h2><ul><li>Oversee permitting, change orders, and project updates.</li><li>Conduct meetings with clients on project progress with clear and concise communication.</li><li>Collaborate with both internal and client teams to develop schedules, daily logs, and reports.</li><li>Oversee construction, design, procurement, schedule, and financial management.</li><li>Utilize client software and databases to update project progress.</li><li>Manage vendors, subcontractors, and general contractors.</li><li>Review documents from the General Contractor before sending them to the client.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in design-build, design, project management, and construction management.</li><li>Experience with change orders, RFIs, and construction documents.</li><li>10+ years of experience in transportation construction and blueprint reading.</li><li>Project experience in aviation or transportation preferred.</li><li>Experience with projects valued at $10 million or more.</li><li>Knowledge of design, either from Design Build General Contractor or Owner&#39;s Representative.</li><li>Ability to create urgency with subcontractors and vendors to advance the project.</li><li>Proficiency in AutoCAD, PowerPoint, and Microsoft Office.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Highly articulate with a clear and analytical approach to problem-solving.</li><li>Strong decision-making abilities.</li><li>Excellent communication and presentation skills.</li><li>Thorough understanding of Project Management, Building Design &amp; Construction.</li><li>Knowledge of Critical Path Method (CPM) Scheduling, Building Cost Modeling, and Risk Analysis.</li><li>Proficiency in Information Technology, including Microsoft Windows OS, Adobe Acrobat, Microsoft Office Suite, and Microsoft Project.</li></ul><h2>Work Environment</h2><p>The position is primarily onsite at Dulles Airport, with the possibility for a hybrid arrangement. The majority of the time will be spent on-site with the end client, five days a week. The company offers a world-leading integrated project and program management consultancy environment, with a culture focused on client and internal staff growth.</p>

<h1><strong><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">Senior</span></span></span></span> Project Manager</strong></h1><p><br></p><h2>Job Description</h2><p>The <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">Senior</span></span></span></span> Project Manager will oversee multiple current and upcoming projects at Dulles Airport, including bathroom upgrades, new baggage claim facilities, and terminal upgrades. This role involves overseeing permitting, change orders, and updates, as well as running meetings with clients to discuss project progress. Collaboration with internal and client teams is essential for developing schedules, daily logs, and reports. The candidate will manage construction, design, procurement, schedule, and financial aspects of the projects.</p><p><br></p><h2>Responsibilities</h2><ul><li>Oversee permitting, change orders, and project updates.</li><li>Conduct meetings with clients on project progress with clear and concise communication.</li><li>Collaborate with both internal and client teams to develop schedules, daily logs, and reports.</li><li>Oversee construction, design, procurement, schedule, and financial management.</li><li>Utilize client software and databases to update project progress.</li><li>Manage vendors, subcontractors, and general contractors.</li><li>Review documents from the General Contractor before sending them to the client.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in design-build, design, project management, and construction management.</li><li>Experience with change orders, RFIs, and construction documents.</li><li>10+ years of experience in transportation construction and blueprint reading.</li><li>Project experience in aviation or transportation preferred.</li><li>Experience with projects valued at $10 million or more.</li><li>Knowledge of design, either from Design Build General Contractor or Owner&#39;s Representative.</li><li>Ability to create urgency with subcontractors and vendors to advance the project.</li><li>Proficiency in AutoCAD, PowerPoint, and Microsoft Office.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Highly articulate with a clear and analytical approach to problem-solving.</li><li>Strong decision-making abilities.</li><li>Excellent communication and presentation skills.</li><li>Thorough understanding of Project Management, Building Design &amp; Construction.</li><li>Knowledge of Critical Path Method (CPM) Scheduling, Building Cost Modeling, and Risk Analysis.</li><li>Proficiency in Information Technology, including Microsoft Windows OS, Adobe Acrobat, Microsoft Office Suite, and Microsoft Project.</li></ul><h2>Work Environment</h2><p>The position is primarily onsite at Dulles Airport, with the possibility for a hybrid arrangement. The majority of the time will be spent on-site with the end client, five days a week. The company offers a world-leading integrated project and program management consultancy environment, with a culture focused on client and internal staff growth.</p>

<p><strong>Description</strong></p><p>- Perform dimensional and visual inspections on critical medical device components or assemblies using various measurement tools like calipers, micrometers, vision inspection equipment, gauges, etc.</p><p>- Conduct functional tests and verify conformance to detailed specifications and tolerances</p><p>- Interpret engineering drawings, specifications, and work instructions</p><p>- Record and maintain accurate inspection data, including lot history and traceability records</p><p>- Support lot release, material review, and root cause analysis for nonconforming parts</p><p>- Participate in audits and provide complete, well-organized inspection documentation</p><p>- Assist in implementing corrective actions and reinforcing compliance with ISO 13485 and FDA regulations</p><p>- Ensuring adherence to GDP (Good Documentation Practices) and GMP (Good Manufacturing Practices) requirements</p><p>- Nonconformance, CAPA, and Material Review Board Support</p><p><br></p><p><strong>Additional Skills &amp; Qualifications</strong></p><p>- Minimum 3–5 years of quality technical experience in the medical device industry required.</p><p>- Proven experience inspecting critical or high-precision components and/or devices.</p><p>- Familiarity with ISO 13485, and Good Documentation Practices (GDP).</p><p>- Proficiency with inspection equipment and interpreting engineering drawings and GD&amp;T.</p><p>- Experience using Excel, electronic QMS platforms (e.g., Minitab, ETQ, Master Control), and document control systems.</p><p>- Excellent attention to detail, organization, and communication skills.</p><p><br></p><p><strong>Preferred Qualifications:</strong></p><p>- CQI or CQT certification</p><p>- Experience with cleanroom manufacturing in a medical device setting.</p><p>- Working knowledge of SPC and data analysis tools such as Minitab.</p><p>- Familiarity with Failure Investigation techniques.</p><p><br></p><p><br></p><p><br></p>

Senior Quality Inspector

<h1><strong>Job Title: <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">Senior</span></span></span> R&amp;D Engineer, DFX</strong></h1><p><br></p><h2>Job Description</h2><p>This mechanical engineering role focuses on applying Design for Excellence (DFX) principles, particularly Design for Manufacturability (DFM), to enhance product development by reducing manufacturing costs, improving quality, and streamlining production. The engineer will collaborate with contract manufacturers to create scalable processes through adaptable systems that efficiently increase production volumes while maintaining quality and controlling expenses. A strong understanding of current design technology is essential, as the engineer will be involved in new product development projects to establish high-quality mechanical designs, rapid prototype development, design input requirements, risk documentation, test methods, and verification testing. This role requires interfacing across multiple departments including manufacturing, production, supply chain, quality, regulatory, and other engineering teams.</p><p><br></p><h2>Responsibilities</h2><ul><li>Develop mechanical designs for new product development projects and current product enhancements focusing on manufacturable, scalable, and cost-effective solutions.</li><li>Build and test preliminary ideas using rapid prototyping tools to evaluate design concepts and iterate toward final solutions.</li><li>Conduct risk management documentation, including hazard analysis and failure modes and effects analyses (FMEA/FMECA), to identify and mitigate design and process risks.</li><li>Lead root cause analysis investigations for product failures and test anomalies using structured approaches such as 5 Whys, fishbone diagram, design of experiments (DOE), and statistical analysis.</li></ul><h2>Essential Skills</h2><ul><li>Expertise in medical device design.</li><li>Proficiency in Design for Excellence (DFX) and Design for Manufacturability (DFM).</li><li>Experience in cost optimization and design control.</li><li>Skills in prototype development, root cause analysis, FMEA, FMECA, and DHF.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Proficiency in CAD tools, such as SolidWorks.</li><li>Experience with CNC Machining and 3D Printing.</li></ul><h2>Work Environment</h2><p>The work environment involves collaboration across multiple departments including manufacturing, production, supply chain, quality, and regulatory engineering teams. The role requires the use of technologies like CAD tools and rapid prototyping equipment in a setting that emphasizes scalability and cost-effectiveness.</p>

Senior R&D Engineer, DFX

<h1><strong>Job Title: <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">Senior</span></span></span></span></span> R&amp;D Engineer - Shelf-life Testing</strong></h1><p><br></p><h2>Job Description</h2><p>As a <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">Senior</span></span></span></span></span> R&amp;D Engineer, you will play a crucial role in assisting the engineering team with enhancing the shelf life of products and meeting manufacturing requirements. You will be involved in product cycles, understanding product interactions with end clients, and ensuring compliance with industry standards.</p><p><br></p><h2>Responsibilities</h2><ul><li>Extend the shelf life for products, particularly catheters.</li><li>Redefine or remediate product requirements to align with clinical needs and standards.</li><li>Conduct shelf-life testing, with a preference for catheter shelf-life testing.</li><li>Participate in design verification and validation processes.</li><li>Utilize Instron pull test machines for testing.</li><li>Conduct Design of Experiments (DOEs) testing.</li><li>Use SolidWorks to design couplers for connecting multiple catheters.</li></ul><h2>Essential Skills</h2><ul><li>Experience with medical devices.</li><li>Proficiency in shelf life testing.</li><li>Understanding of product requirements and their clinical relevance.</li><li>Experience with design verification and validation processes.</li><li>Familiarity with Instron pull test machines.</li><li>Ability to conduct DOEs testing.</li><li>SolidWorks proficiency.</li><li>5-7 years of relevant experience.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience in injection molding is desirable.</li><li>Experience through 1-2 product cycles.</li></ul><h2>Work Environment</h2><p>The role is set in a dynamic startup environment with approximately 80-100 employees. Recently, the company received FDA 510(k) clearance and is entering the commercialization phase, with plans to expand R&amp;D and manufacturing facilities by moving into a second building soon.</p>

Senior R&D Engineer, Mechanical Shelf-Life

<h1><strong>Job Title: R&amp;D Engineer</strong></h1><p><br></p><h2>Job Description</h2><p>This position supports the design and development of product changes within sustaining engineering and new product development for disposable medical devices. The role requires expertise in medical device design, focusing on Class II and Class III disposable products.</p><p><br></p><h2>Responsibilities</h2><ul><li>Design and develop product modifications and innovations within sustaining engineering projects.</li><li>Lead new product development initiatives for disposable medical devices.</li><li>Ensure compliance with FDA Design Controls and ISO Quality Management Systems.</li><li>Apply risk management practices as per ANSI/AAMI/ISO standards in medical device development.</li><li>Collaborate with cross-functional teams to optimize product design and functionality.</li></ul><h2>Essential Skills</h2><ul><li>Bachelor&#39;s degree in Mechanical, Plastics, Biomedical Engineering, or a related field; Master&#39;s degree preferred.</li><li>Minimum of 5 years of experience in Class II or Class III disposables medical product development.</li><li>Proficiency in Design for Six Sigma (DFSS) principles.</li><li>Strong knowledge of plastics materials and processing, including injection molding, extrusion, ultrasonic welding, UV/solvent bonding, and sterilization.</li><li>Proficiency in CAD design and PDM enterprise software, such as Creo and Solidworks.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Certification in Design for Six Sigma (DFSS) is highly desirable.</li><li>Experience with FDA Design Controls and ISO Quality Management Systems.</li><li>Familiarity with ANSI/AAMI/ISO standards related to medical device risk management.</li></ul><h2>Work Environment</h2><p>The position <strong><u>offers a hybrid work</u></strong> environment, allowing remote work on Mondays and Fridays, with in-office presence required on Tuesdays, Thursdays, and Fridays. Core working hours are from 9 AM to 3 PM.</p>

Senior R&d Engineer

<h1><strong>Job Title: Research Associate</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a Research Associate with a focus on qPCR optimization and assay development. This role involves working primarily on the bench, performing DNA extractions and PCR sequencing using blood samples. The position offers ample opportunities to learn molecular techniques and automate processes within a dynamic biotech environment.</p><p><br></p><h2>Responsibilities</h2><ul><li>Perform experiments and procedures in accordance with written protocols.</li><li>Assist in developing protocols and procedures.</li><li>Document, report, and present results of experiments and procedures.</li><li>Follow work instructions and SOPs as required by ISO quality management systems.</li><li>Assist in maintaining laboratory inventory and equipment.</li><li>Work collaboratively within the platform integration team and cross-functionally with other teams.</li><li>Contribute to the success of the entire project through effective problem-solving and communication.</li></ul><h2>Essential Skills</h2><ul><li>3-5 years of experience in applicable life sciences such as Molecular Biology, Biochemistry, Microbiology, Chemistry, or Immunology.</li><li>Proficiency in nucleic acid techniques including DNA extraction, purification, quantification, qPCR, and PCR multiplex.</li><li>Experience with molecular biology sample preparation using magnetic particles.</li><li>Competency in data interpretation and analysis.</li><li>Knowledge of standard laboratory techniques such as aseptic technique.</li><li>Ability to work with human blood samples.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor&#39;s Degree in Biology, Chemistry, or other relevant field with 3-5 years of experience.</li><li>Master&#39;s Degree in Biology, Chemistry, or other relevant field with 1+ years industry experience.</li><li>Experience working in a BSL-2 environment with live organisms is a plus.</li><li>Competency with Microsoft Office Suite (MS Word, Excel, PowerPoint).</li><li>Excellent organizational and project management skills.</li><li>Ability to plan and execute experiments with minimal assistance.</li></ul><h2>Work Environment</h2><p>The role is part of a seven-member integration team within a larger group of seventeen professionals. The work environment includes administration, laboratory, and manufacturing settings. The position requires working in the lab 90% of the time with flexible hours, starting no later than 8:30 AM. The company culture is supportive, with kind and personable colleagues, and offers flexible work times to accommodate personal needs.</p>

Senior Research Associate

<h2><strong>Seeking Lead Resident Engineers For a leading NYC infrastructure firm that offers the opportunity to work on impactful public projects.</strong></h2><p><br></p><h2>Job Description</h2><p>We are seeking a Lead Resident Engineer will conduct site inspections to verify that utility installations and relocations meet project requirements and industry standards, approve work completed by contractors, and recommend acceptance or necessary corrective action. Additionally, this role involves monitoring utility-related costs and ensuring adherence to project budgets.</p><p><br></p><h2>Responsibilities</h2><ul><li>Coordinate relocations, new installations, and service adjustments.</li><li>Oversee utility-related construction to ensure adherence to design plans, specifications, and safety standards.</li><li>Conduct site inspections to verify that utility installations and relocations meet project requirements and industry standards.</li><li>Approve work completed by contractors and recommend acceptance or necessary corrective action.</li><li>Monitor utility-related costs and ensure adherence to project budgets.</li></ul><h2>Essential Skills</h2><ul><li>Professional Engineer (PE) license.</li><li>Bachelor&#39;s degree in Civil Engineering or a related field.</li><li>Minimum of 10 years of experience in heavy civil construction infrastructure projects.</li><li>Experience coordinating relocations, new installations, and service adjustments for water, sewer, gas, and electric systems.</li><li>Experience with infrastructure projects.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with Large Scale Infrastructure or Transportation related projects.</li><li>Experience with local utility companies and municipal agencies.</li></ul>

Senior Resident Engineer

<p>Position Summary:</p><p>As a <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">Senior</span></span> Fermentation Technician, you will oversee and execute fermentation processes in a large-scale industrial setting. You will be responsible for monitoring and optimizing fermentation parameters, ensuring product quality, and mentoring junior operators.</p><p><br></p><p>Key Responsibilities:</p><p><br></p><p>Operate and monitor fermentation equipment and systems.</p><p>Prepare media, inoculate fermenters, and manage fermentation cycles.</p><p>Collect and analyze samples to monitor fermentation progress.</p><p>Troubleshoot process deviations and implement corrective actions.</p><p>Maintain accurate batch records and documentation.</p><p>Ensure compliance with safety, quality, and regulatory standards.</p><p>Collaborate with R&amp;D and quality teams to improve processes.</p><p>Train and mentor junior staff and new hires.</p><p><br></p><p>Qualifications:</p><p><br></p><p>Associate’s or Bachelor’s degree in Microbiology, Biotechnology, Biochemistry, or related field.</p><p>3–5+ years of experience in industrial fermentation or bioprocessing.</p><p>Strong understanding of microbial growth, aseptic techniques, and fermentation control.</p><p>Experience with SCADA or other process control systems.</p><p>Ability to work in a fast-paced, team-oriented environment.</p><h1><br></h1>

Senior Scientist

<blockquote><p class="ql-quote-block">We are seeking a Scientist to join our Analytical Method Development team. In this critical role, you will serve as aSubject Matter Expert (SME) in analytical method transfer and validation, supporting the development and quality control of lipid nanoparticles (LNPs). You will also play a key role in continuous improvement initiatives and provide technical leadership in investigations and root cause analyses.</p><p class="ql-quote-block"><br></p><p class="ql-quote-block">Please note:This role will evenutally need to relocate to North Dakota. Relocation assistance is available.</p></blockquote><hr><h3>Key Responsibilities:</h3><ul><li>Act as SME for analytical method transfer and validation.</li><li>Support method and process validation activities.</li><li>Contribute to QC testing and development for lipid nanoparticles (LNPs).</li><li>Lead or support investigations into deviations, OOS results, and CAPAs.</li><li>Drive continuous improvement in analytical methodologies and lab practices.</li><li>Mentor and support the development of junior scientists.</li></ul><hr><h3>Required Skills &amp; Expertise:</h3><ul><li>Strong <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">background</span></span></span> inanalytical chemistry,method development, andquality control.</li><li>Hands-on experience withHPLC,capillary electrophoresis,PCR, andprotein assays.</li><li>Proficiency inELISA,protein chemistry, and regulatory compliance (e.g., FDA guidelines).</li><li>Demonstrated ability to troubleshoot and optimize analytical methods.</li></ul><hr><h3>Qualifications:</h3><ul><li>PhDin a relevant scientific discipline with5+ yearsof experience, or</li><li>Master’s degreewith7+ years, or</li><li>Bachelor’s degreewith10+ yearsof relevant experience.</li><li>Proven experience mentoring junior team members is highly desirable.</li></ul><hr><h3>Work Environment:</h3><ul><li>100% onsiterole, Monday–Friday, 9:00 AM – 5:00 PM.</li><li>Individual contributor role with mentoring responsibilities.</li><li>Reports to theSr. Manager of Method Validation.</li><li>Collaborative team environment with nine scientists.</li></ul>

<blockquote><p class="ql-quote-block">We are seeking a Scientist to join our Analytical Method Development team. In this critical role, you will serve as aSubject Matter Expert (SME) in analytical method transfer and validation, supporting the development and quality control of lipid nanoparticles (LNPs). You will also play a key role in continuous improvement initiatives and provide technical leadership in investigations and root cause analyses.</p><p class="ql-quote-block"><br></p><p class="ql-quote-block">Please note:This role will evenutally need to relocate to North Dakota. Relocation assistance is available.</p></blockquote><hr><h3>Key Responsibilities:</h3><ul><li>Act as SME for analytical method transfer and validation.</li><li>Support method and process validation activities.</li><li>Contribute to QC testing and development for lipid nanoparticles (LNPs).</li><li>Lead or support investigations into deviations, OOS results, and CAPAs.</li><li>Drive continuous improvement in analytical methodologies and lab practices.</li><li>Mentor and support the development of junior scientists.</li></ul><hr><h3>Required Skills &amp; Expertise:</h3><ul><li>Strong <span style="color: rgb(8, 7, 7); background-color: none;">background</span> inanalytical chemistry,method development, andquality control.</li><li>Hands-on experience withHPLC,capillary electrophoresis,PCR, andprotein assays.</li><li>Proficiency inELISA,protein chemistry, and regulatory compliance (e.g., FDA guidelines).</li><li>Demonstrated ability to troubleshoot and optimize analytical methods.</li></ul><hr><h3>Qualifications:</h3><ul><li>PhDin a relevant scientific discipline with5+ yearsof experience, or</li><li>Master’s degreewith7+ years, or</li><li>Bachelor’s degreewith10+ yearsof relevant experience.</li><li>Proven experience mentoring junior team members is highly desirable.</li></ul><hr><h3>Work Environment:</h3><ul><li>100% onsiterole, Monday–Friday, 9:00 AM – 5:00 PM.</li><li>Individual contributor role with mentoring responsibilities.</li><li>Reports to theSr. Manager of Method Validation.</li><li>Collaborative team environment with nine scientists.</li></ul>

<blockquote><p class="ql-quote-block">We are seeking a Scientist to join our Analytical Method Development team. In this critical role, you will serve as aSubject Matter Expert (SME) in analytical method transfer and validation, supporting the development and quality control of lipid nanoparticles (LNPs). You will also play a key role in continuous improvement initiatives and provide technical leadership in investigations and root cause analyses.</p><p class="ql-quote-block"><br></p><p class="ql-quote-block">Please note:This role will evenutally need to relocate to North Dakota. Relocation assistance is available.</p></blockquote><hr><h3>Key Responsibilities:</h3><ul><li>Act as SME for analytical method transfer and validation.</li><li>Support method and process validation activities.</li><li>Contribute to QC testing and development for lipid nanoparticles (LNPs).</li><li>Lead or support investigations into deviations, OOS results, and CAPAs.</li><li>Drive continuous improvement in analytical methodologies and lab practices.</li><li>Mentor and support the development of junior scientists.</li></ul><hr><h3>Required Skills &amp; Expertise:</h3><ul><li>Strong <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">background</span></span> inanalytical chemistry,method development, andquality control.</li><li>Hands-on experience withHPLC,capillary electrophoresis,PCR, andprotein assays.</li><li>Proficiency inELISA,protein chemistry, and regulatory compliance (e.g., FDA guidelines).</li><li>Demonstrated ability to troubleshoot and optimize analytical methods.</li></ul><hr><h3>Qualifications:</h3><ul><li>PhDin a relevant scientific discipline with5+ yearsof experience, or</li><li>Master’s degreewith7+ years, or</li><li>Bachelor’s degreewith10+ yearsof relevant experience.</li><li>Proven experience mentoring junior team members is highly desirable.</li></ul><hr><h3>Work Environment:</h3><ul><li>100% onsiterole, Monday–Friday, 9:00 AM – 5:00 PM.</li><li>Individual contributor role with mentoring responsibilities.</li><li>Reports to theSr. Manager of Method Validation.</li><li>Collaborative team environment with nine scientists.</li></ul>

<h1><strong><span style="color: rgb(8, 7, 7); background-color: none;">Senior</span> Scientist</strong></h1><p><br></p><h2>Job Description</h2><p>The <span style="color: rgb(8, 7, 7); background-color: none;">Senior</span> Scientist is responsible for supporting all aspects of Good Manufacturing Practices (GMP) and production in the Clinical Manufacturing Facility (CMF). Working collaboratively with GMP Operations management and staff, the role provides hands-on assistance for day-to-day GMP production operations. This includes executing production processes, maintaining documentation, and ensuring facility and equipment maintenance. The position supports production efforts to deliver products in a timely, compliant, and fiscally responsible manner by adhering to appropriate practices, batch records, and Standard Operating Procedures (SOPs) for manufacturing biological products.</p><p><br></p><h2>Responsibilities</h2><ul><li>Conduct 50-75% lab work, focusing on research-grade production, biology tissue culture, solution preparation, and assay management.</li><li>Support paperwork and preparation for subsequent process steps, constituting approximately 25% of duties.</li><li>Collaborate with management and staff to determine the strategic direction of the GMP area, including scheduling and project timelines.</li><li>Maintain GMP resources and supply chain, ensuring materials inventory control to meet production goals.</li><li>Operate, calibrate, validate, and clean facility equipment and systems as specified in SOPs.</li><li>Assist in reviewing, revising, and remediating process documentation, and managing process change controls.</li><li>Work closely with GMP Management to identify and meet continuous improvement objectives using metrics and statistical methods.</li><li>Involved in making and developing viruses and some process development work.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in GMP, tissue, virology, biology, cell culture, solution preparation, microbiology, and mammalian cell culture.</li><li>Experience with eukaryotic cells, PCR, and assays.</li><li>Bachelor&#39;s degree in a life science field such as biochemistry, microbiology, or virology.</li><li>Minimum of 1+ years of experience in the scientific industry from a GMP or GLP setting.</li><li>Knowledge of aseptic techniques, cell culture, liquid separation techniques, and fluid handling.</li><li>Hands-on experience with mammalian or eukaryotic cells, gained either professionally or academically.</li><li>Chromatography experience and solution/buffer preparation skills.</li><li>Alliquoting experience and understanding of cell culture, transfections, suspension cells, or adherent cells.</li><li>Knowledge of GMP or bioprocessing.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with purification techniques.</li><li>Additional GMP experience.</li></ul><h2><br></h2>

<h1><strong>Job Title: Sr Scientist</strong></h1><p><br></p><h2>Job Description</h2><p>Join our team as a Sr Scientist, where you will support the Analytical Method Development Team as a Subject Matter Expert. You will be instrumental in test method transfer, analytical test method validation, and driving continuous improvement initiatives. Your expertise will also contribute to test method validation, process validation, and QC testing and development on lipid nanoparticles (LNPs). Additionally, you will support deviations and investigations for Out of Specification (OOS) results, Corrective and Preventive Actions (CAPA), and root cause analysis.</p><p><br></p><h2>Responsibilities</h2><ul><li>Serve as a Subject Matter Expert for test method transfer and analytical test method validation.</li><li>Assist with test method validation and process validation.</li><li>Support QC testing and development on lipid nanoparticles (LNPs).</li><li>Investigate deviations and support OOS, CAPA, and root cause analysis.</li><li>Drive continuous improvements in processes and methodologies.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in method development, analytical chemistry, and quality control.</li><li>Experience with HPLC, validation, LNP, and protein assays.</li><li>Strong knowledge of analytical method development, protein chemistry, ELISA, capillary electrophoresis, FDA regulations, and PCR.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor&#39;s degree with 10+ years of experience, Master&#39;s degree with 7+ years of experience, or PhD with 5+ years of experience.</li><li>Understanding of HPLC, capillary electrophoresis, and PCR.</li><li>Experience mentoring and supporting the development of junior scientists.</li></ul><h2>Work Environment</h2><p>This role is 100% onsite, operating Monday to Friday from 9:00 am to 5:00 pm. You will be an individual contributor with responsibilities to mentor other scientists, working within a team of nine and reporting directly to the Sr Manager of Method Validation. High degrees of collaboration and communication skills are essential in this dynamic and growth-oriented environment</p>

<blockquote><p class="ql-quote-block">We are seeking a Scientist to join our Analytical Method Development team. In this critical role, you will serve as a Subject Matter Expert (SME) in analytical method transfer and validation, supporting the development and quality control of lipid nanoparticles (LNPs). You will also play a key role in continuous improvement initiatives and provide technical leadership in investigations and root cause analyses.</p><p class="ql-quote-block"><br></p><p class="ql-quote-block">Please note: This role will eventually need to relocate to North Dakota. Relocation assistance is available.</p></blockquote><hr><h3>Key Responsibilities:</h3><ul><li>Act as SME for analytical method transfer and validation.</li><li>Support method and process validation activities.</li><li>Contribute to QC testing and development for lipid nanoparticles (LNPs).</li><li>Lead or support investigations into deviations, OOS results, and CAPAs.</li><li>Drive continuous improvement in analytical methodologies and lab practices.</li><li>Mentor and support the development of junior scientists.</li></ul><hr><h3>Required Skills &amp; Expertise:</h3><ul><li>Strong experience in analytical chemistry, method development, and quality control.</li><li>Hands-on experience with HPLC, capillary electrophoresis, PCR, and protein assays.</li><li>Proficiency in ELISA, protein chemistry, and regulatory compliance (e.g., FDA guidelines).</li><li>Demonstrated ability to troubleshoot and optimize analytical methods.</li></ul><hr><h3>Qualifications:</h3><ul><li>PhD in a relevant scientific discipline with5+ years of experience, or</li><li>Master’s degreewith7+ years, or</li><li>Bachelor’s degreewith10+ years of relevant experience.</li><li>Proven experience mentoring junior team members is highly desirable.</li></ul><hr><h3>Work Environment:</h3><ul><li>100% onsite role, Monday–Friday, 9:00 AM – 5:00 PM.</li><li>Individual contributor role with mentoring responsibilities.</li><li>Reports to the Sr. Manager of Method Validation.</li><li>Collaborative team environment with nine scientists.</li></ul>

<p>We are actively hiring for a <span style="background-color: none; color: rgb(8, 7, 7);">Sr.</span> Scientist to join our expanding optimization team. This individual will play a key role in advancing greener, enzyme-optimized detergents. You&#39;ll drive detergent optimization projects in close collaboration with customers and global teams, helping shape new capabilities within our technical service function. A strong experience with detergent applications, formulations (liquids and unit dose), and industry knowledge is essential, as we focus on innovation, digitalization, and sustainable solutions.</p><p><br></p><p><strong>Description</strong></p><p>- Lead scientific progress and customer interactions within the household care sector.</p><p>- Collaborate with global teams in R&amp;D, formulation centers, marketing, and sales.</p><p>- Develop and apply ingredient, formulation, and process understanding for detergent systems.</p><p>- Deliver innovative services and technical solutions that create significant customer value.</p><p>- Work with enzymes in detergent formulations; experience with solid detergent formats is a plus.</p><p>- Perform data analysis using advanced statistical tools and generate technical reports.</p><p>- Build expertise in ingredient interactions and their synergy with enzyme-based solutions.</p><p>- Independently lead technical projects and mentor junior team members.</p><p>- Contribute to a collaborative, agile work environment with a focus on sustainability and digital innovation.</p><p><br></p><p><strong>Skills &amp; Qualifications</strong></p><p>- M.Sc. or Ph.D. in Chemical/Biochemical Engineering, or related field with relevant experience in industrial application of detergents </p><p>- Working experience (+10 years) in the household/home care industry or similar and understanding</p><p>- Strong experience with detergent applications and formulation (liquids and unit dose).</p><p>- Experience with enzyme-based formulations is highly desirable.</p><p>- Excellent communication and project management skills.</p><p>- Strong experimental and analytical skills.</p><p>- Ability to work cross-functionally and deliver in a fast-paced, global environment.</p><p>- Familiarity with agile methodologies and product ownership is a plus.</p><p><br></p>

<h1><strong>Job Title: Software Engineer</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a talented Software Engineer to join our dynamic team. The role involves developing high-quality software solutions for warehouse control systems and other material handling applications. This position offers an exciting opportunity to work on innovative projects, collaborate with cross-functional teams, and contribute to continuous improvement initiatives within our organization.</p><p><br></p><h2>Responsibilities</h2><ul><li>Participate in development meetings and code reviews.</li><li>Design, develop, and test high-quality software solutions for warehouse control systems (WCS) and other material handling applications.</li><li>Implement features, enhancements, and integrations based on customer and internal requirements.</li><li>Write clean, efficient, and maintainable code following best practices.</li><li>Assist in the creation of project specifications and design parameters.</li><li>Develop and support custom modules and interfaces with project teams.</li><li>Troubleshoot and resolve complex issues during implementation.</li><li>Review code, designs, and test plans for quality and consistency.</li><li>Travel to site to support software project engineers if required.</li><li>Ensure future development supports existing systems with an upgrade path if needed.</li><li>Provide Tier II support during working hours and potentially after hours.</li><li>Receive feedback for software enhancements to improve system support.</li><li>Identify opportunities to optimize software performance and enhance scalability.</li><li>Stay updated on industry trends and emerging technologies.</li><li>Contribute to the development of internal frameworks and reusable components.</li></ul><h2>Essential Skills</h2><ul><li>Bachelor’s Degree in computer science, engineering, or a related field preferred.</li><li>5+ years of experience in a software engineering environment.</li><li>Experience in managing and supporting software development life cycles.</li><li>Ability to work effectively in a team environment.</li><li>Excellent troubleshooting and customer service skills.</li><li>Proficiency in C# and SQL.</li><li>Understanding of warehouse workflows and integrations.</li><li>Strong verbal and written communication skills.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience in other object-oriented languages such as C++.</li><li>Knowledge of interface methodologies and data formats like sockets, RESTful, SOAP, XML, JSON, and EDI.</li><li>Experience in configuring and troubleshooting IT issues with servers, workstations, and printers.</li><li>Willingness to travel up to 33% of the time.</li></ul><h2><br></h2>

Senior Software Engineer

<h1 style="font-weight: 700;">Job Title: <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">Senior</span></span> Software Engineer</h1><br><h2>Job Description</h2><p>We are seeking a highly skilled <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">Senior</span></span> Software Engineer to develop innovative software solutions that automate product manufacturing, laboratory testing, SQL data storage, and data analysis in a dynamic, customer-focused automotive environment.</p><br><h2>Responsibilities</h2><ul><li>Comply with cybersecurity standards, corporate governance, industry standards, and internal best practices to minimize software risks and eliminate vulnerabilities.</li><li>Utilize the latest source code control methodologies to maintain an organized and well-documented code base.</li><li>Develop enterprise-level data reporting and management solutions.</li><li>Implement continuous improvement initiatives to support internal and customer-focused requirements.</li><li>Plan and deliver timely solutions in a hybrid development environment.</li><li>Lead system architecture, software design, and security reviews.</li><li>Create system and subsystem software documentation.</li><li>Provide mentorship and training to engineers and interns.</li><li>Demonstrate expertise in electromechanical and automation systems.</li><li>Consult on the concept, design, and implementation of hardware solutions to meet testing requirements.</li><li>Provide operational feasibility feedback to manufacturing teams.</li></ul><h2>Essential Skills</h2><ul><li>Expert in TestStand</li><li>Experience in LabVIEW</li><li>5-7 years of experience in software development</li><li>Proficiency in SQL Server</li><li>Strong skills in C++ and .NET</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience in developing software solutions for electromechanical and automation systems</li><li>Ability to lead and conduct security reviews</li><li>Strong documentation skills for system and subsystem software</li></ul><h2>Work Environment</h2><p>The work environment is fast-paced and customer-focused, centered around the automotive industry. The role involves working with state-of-the-art technologies and methodologies in a hybrid development environment, with opportunities for continuous improvement and innovation.</p><br>

<h1><strong style="color: windowtext;">Job Title: Software Engineer</strong></h1><p>Location: Newark, CA</p><p>Job Type: Contract</p><p><br></p><h2><span style="color: windowtext;">Job Summary</span></h2><p>We are seeking a skilled and detail-oriented Software Engineer to join our client. The ideal candidate will be responsible for designing, developing, implementing, testing, and maintaining business and computer applications software, including mainframe and client/server applications. This role also involves enhancing existing systems and delivering high-quality software solutions tailored to client requirements.</p><p><br></p><h2><span style="color: windowtext;">Key Responsibilities</span></h2><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">        </span>Design and implement software solutions across various platforms.</p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">        </span>Gather and analyze system requirements, document technical specifications.</p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">        </span>Write clean, efficient, and well-documented code based on specifications.</p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">        </span>Prepare comprehensive test plans.</p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">        </span>Conduct unit testing and debugging of new and existing programs.</p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">        </span>Create and manage migration packages for system testing, user acceptance testing, and deployment.</p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">        </span>Perform quality assurance reviews and post-implementation validation.</p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">        </span>Troubleshoot and resolve software issues in both new and legacy systems.</p><p><br></p><h2><span style="color: windowtext;">Qualifications</span></h2><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">        </span>Bachelor’s degree in Computer Science, Engineering, or a related field.</p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">        </span>5–7 years of professional experience in software development.</p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">        </span>Strong foundation in computer science, including data structures, algorithms, and software design.</p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">        </span>Proven experience in large systems software design and development.</p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">        </span>Proficient in troubleshooting, debugging, and unit testing.</p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">        </span>Experience with both modern and legacy production systems.</p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">        </span>Excellent problem-solving and analytical skills.</p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">        </span>Strong communication and documentation abilities.</p>

<h1><strong><span style="color: rgb(8, 7, 7); background-color: none;">Senior</span> Software Engineer - Level 5</strong></h1><p><br></p><h2>Job Description</h2><p>The qualified candidate will be responsible for evaluating operational software problems and providing immediate solutions to restore service, as well as integration and verification of new baselines.</p><p><br></p><h2>Responsibilities</h2><ul><li>Support troubleshooting, maintenance, and documentation of software applications.</li><li>Troubleshoot and isolate sources of system errors or unexpected performance.</li><li>Perform testing, integration, and delivery of new software baselines.</li><li>Conduct in-depth analysis and assessment with an end-to-end perspective of a complex system in operations.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in Java and C++.</li><li>Strong <span style="color: rgb(8, 7, 7); background-color: none;">background</span> in software development and software integration.</li><li>Bachelor&#39;s Degree in Science, Technology, Engineering, or Mathematics (STEM).</li><li>Minimum of 8 years of prior relevant experience.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with software configuration management systems such as Git or Bitbucket.</li><li>Ability to work in a structured configuration-controlled environment.</li><li>Linux/Unix, SQL experience.</li><li>Experience with JIRA, BitBucket, and Confluence is desired.</li></ul><h2>Work Environment</h2><p>The work environment is primarily focused on the support and maintenance of real-time software applications on an Operations and Maintenance (O&amp;M) contract. This role will involve working in a structured configuration-controlled setting</p>

Senior Software Engineer - Level 5

<h1><strong>Sr. Software Engineer - Unreal</strong></h1><h2>Job Description</h2><p>As a Software Engineer specializing in Unreal Engine, you will play a pivotal role in shaping innovative solutions from concept to implementation. You will be responsible for designing and developing Unreal Engine applications and advanced immersive technologies. Collaborating closely with a team of experts in a dynamic environment, you will tackle complex challenges, optimize performance, and ensure seamless integration with various real-time platforms. Your contributions will help drive the evolution of spatial computing, enhancing user experiences and pushing the boundaries of what&#39;s possible in this exciting field.</p><p><br></p><h2>Responsibilities</h2><ul><li>Solve complex problems in real-time systems using Unreal Engine, sensor fusion, simulation, and spatial computing.</li><li>Contribute to the design and development of innovative solutions for client projects and internal products.</li><li>Participate in code reviews, design discussions, and knowledge sharing to foster a culture of continuous improvement.</li><li>Collaborate with cross-functional team members to drive project success and enhance client experiences.</li></ul><h2>Essential Skills</h2><ul><li>5+ years of experience and Deep experience working in the Unreal Engine and several native features such as Replication, Mass, and Chaos.</li><li>Proficiency in C++ programming from scratch and Blueprints Visual Scripting.</li><li>Experience in training, simulation, and gaming industries.</li><li>Familiarity with various headsets including Meta Quest, HTC Vive, Magic Leap, Apple Vision Pro.</li><li>Experience in augmented reality (AR) and virtual reality (VR) technologies.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience in a high-autonomy startup environment, showcasing adaptability and discipline.</li><li>Enthusiasm for innovation in immersive experiences and a drive to constantly push creative boundaries.</li></ul><h2>Work Environment</h2><p>Due to the nature of the work being completed, must  be able to comply with government regulations. Our projects involve hands-on work with specialized hardware at our lab, so it&#39;s essential that you reside in or near the Orlando, FL area and can commute as needed.</p>

Senior Software Engineer - Unreal Engine

<h1><strong>Sr. Software Engineer - Unreal</strong></h1><p><br></p><h2>Job Description</h2><p>As a Software Engineer specializing in Unreal Engine, you will play a pivotal role in shaping innovative solutions from concept to implementation. You will be responsible for designing and developing Unreal Engine applications and advanced immersive technologies. Collaborating closely with a team of experts in a dynamic environment, you will tackle complex challenges, optimize performance, and ensure seamless integration with various real-time platforms. Your contributions will help drive the evolution of spatial computing, enhancing user experiences and pushing the boundaries of what&#39;s possible in this exciting field.</p><p><br></p><h2>Responsibilities</h2><ul><li>Solve complex problems in real-time systems using Unreal Engine, sensor fusion, simulation, and spatial computing.</li><li>Contribute to the design and development of innovative solutions for client projects and internal products.</li><li>Participate in code reviews, design discussions, and knowledge sharing to foster a culture of continuous improvement.</li><li>Collaborate with cross-functional team members to drive project success and enhance client experiences.</li></ul><h2>Essential Skills</h2><ul><li>Deep experience working in the Unreal Engine and several native features such as Replication, Mass, and Chaos.</li><li>Proficiency in C++ and Blueprints Visual Scripting.</li><li>Experience in training, simulation, and gaming industries.</li><li>Familiarity with various headsets including Meta Quest, HTC Vive, Magic Leap, Apple Vision Pro.</li><li>Experience in augmented reality (AR) and virtual reality (VR) technologies.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience in a high-autonomy startup environment, showcasing adaptability and discipline.</li><li>Enthusiasm for innovation in immersive experiences and a drive to constantly push creative boundaries.</li></ul><h2>Work Environment</h2><p>Due to the nature of the work being completed, must  be able to comply with government regulations. Our projects involve hands-on work with specialized hardware at our lab, so it&#39;s essential that you reside in or near the Orlando, FL area and can commute as needed.</p>

<h1><strong>Job Title: Software Manufacturing Process Engineer</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a LabVIEW Developer to lead manufacturing test systems development efforts. This position supports our new product design initiatives by developing manufacturing and test systems, creating and improving processes within the team, and ensuring adherence to all processes. As part of a project team, you will collaborate on product design with an emphasis on manufacturability to fulfill lean manufacturing objectives for electronic assemblies such as joysticks, controllers, displays, and sensors for off-road equipment.</p><p><br></p><h2>Responsibilities</h2><ul><li>Lead development of process controls and functional tests in the LabVIEW programming environment.</li><li>Recommend new technologies including AI, VR, robotics, and light-guided assembly to improve manufacturing quality and efficiency.</li><li>Develop and maintain product configuration tools.</li><li>Understand requirements for production through knowledge of embedded and application software.</li><li>Lead design of production cells for new product introductions, including assembly automation, testing, and packaging.</li><li>Develop and approve specifications, implement processes for assembly and testing of new/revised products, establish goals, train team members, and evaluate results.</li><li>Design, develop, test, source, and cost-justify various tools, machinery, and equipment for recommended manufacturing methods.</li><li>Confer with vendors to determine product specifications and arrange for the purchase of machinery and equipment according to specifications and quality standards.</li><li>Prepare project documentation, including diagrams or layouts.</li><li>Provide verbal or written project status reports to project teams, management, subcontractors, or customers.</li></ul><h2>Requirements</h2><ul><li>Bachelor&#39;s degree in Electrical Engineering or Computer Engineering, or related engineering field.</li><li>4+ years of experience with LabVIEW.</li><li>4+ years of developing test systems for manufacturing environments.</li><li>Experience in developing complex LabVIEW test systems from scratch.</li><li>Familiarity with additional software systems such as Python, C++, and C#.</li><li>Nice to have: LabVIEW Development, Test Stand, National Instruments experience.</li><li>CLD Certified LabVIEW Developer and CLA Certified LabVIEW Architect.</li><li>Software development skills (LabVIEW, Python, C#, C++).</li><li>Database architecture design for storing and analyzing production information.</li><li>Proficiency in SVN or other code management systems for source code control.</li><li>Expertise in communication protocols (CAN) and debugging techniques.</li><li>Experience with Mechanical/Electrical drawings for industrial equipment.</li><li>Informal leadership skills for guiding team members to accomplish project tasks.</li><li>Ability to manage tasks and collaborate on project schedules.</li><li>Ability to identify and drive improvement initiatives within the team.</li><li>Effective communication skills for conveying information to development engineers, production operators, and management teams.</li><li>Ability to define problems, collect data, establish facts, and draw valid conclusions.</li><li>Ability to interpret extensive technical instructions in mathematical or diagram form and handle abstract and concrete variables.</li><li>Ability to read and interpret test specifications and electrical schematics for determining proper test methodology.</li></ul>

Senior Software Manufacturing Process Engineer

<p><strong>Description</strong></p><p>Will help lead the structural engineering team, providing leadership, mentoring, and oversight of work given to junior staff.   Will work on the analysis and design of various commercial, institutional, and/or industrial buildings, and will include structural steel, reinforced concrete, and masonry.   Will develop designs, drawings, and specifications for the main building structural frame and foundations.    Will sign off on drawings and be responsible for the construction administration.   Will use Revit and RISA.    This can be a hybrid role, and their policy is 4 days remote, 1 day in office for experienced engineers, 4 days in office for junior/entry-level.  Can be flexible on this depending on the experience of the candidates.  Could include occasional travel to job sites. If person has PE and 10 years or more of experience, they could consider a fully remote person.</p><p><br></p><p><strong>Additional Skills &amp; Qualifications</strong></p><p>MUST HAVES:</p><p>Bachelors in Civil Engineering with a Structural focus</p><p>5-10+ years of experience</p><p>Relevant project experience: Industrial, Institutional, and/or Commercial projects</p><p>Revit experience</p><p>RISA3D and/or RISAFloor experience</p><p>PE or ability to obtain one in 6-12 months</p><p><br></p><p>BONUS:</p><p>Masters degree</p><p>Michigan PE license</p><p>12 plus years of experience</p>

Senior Structural Engineer

<p><strong>Job Description:</strong></p><p>We are urgently hiring a <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">Senior</span></span></span> Superintendent with SCIF, clean room, or semiconductor experience. This company works on aerospace &amp; defense, higher education, government, industrial, and other project types. This company was founded over 100 years ago and operates in 34 states.</p><p><br></p><p><strong>Why You Should Be Interested:</strong></p><ul><li>Starting salary of $150K+</li><li>Company truck + gas card</li><li>Bonuses</li><li>Flex time every other week</li><li>Competitive PTO, 401k match, and other benefits</li></ul><p><strong>Qualifications:</strong></p><ul><li>10+ years of experience as a Superintendent at a GC</li><li>Ground-up commercial experience ranging from $15-35M</li><li>Experience with at least 1 SCIF, clean room, or semiconductor project</li></ul><p><strong>Work Environment:</strong></p><p>Projects in Denver Metro – Boulder, Golden, Thornton, and surrounding areas. 12 Superintendents total.</p><p><br></p><p><strong>Salary Range: </strong></p><p>Starting at $150,000</p>

Senior Superintendent

<p><strong>Job Description:</strong></p><p>We are urgently hiring a <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">Senior</span></span></span></span> Superintendent with SCIF, clean room, or semiconductor experience. This company works on aerospace &amp; defense, higher education, government, industrial, and other project types. This company was founded over 100 years ago and operates in 34 states.</p><p><br></p><p><strong>Why You Should Be Interested:</strong></p><ul><li>Starting salary of $150K+</li><li>Company truck + gas card</li><li>Bonuses</li><li>Flex time every other week</li><li>Competitive PTO, 401k match, and other benefits</li></ul><p><strong>Qualifications:</strong></p><ul><li>10+ years of experience as a Superintendent at a GC</li><li>Ground-up commercial experience ranging from $15-35M</li><li>Experience with at least 1 SCIF, clean room, or semiconductor project</li></ul><p><strong>Work Environment:</strong></p><p>Projects in Denver Metro – Boulder, Golden, Thornton, and surrounding areas. 12 Superintendents total.</p><p><br></p><p><strong>Salary Range: </strong></p><p>Starting at $150,000</p>

<h1><strong>Job Title: Systems Engineer</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a Systems Engineer responsible for developing electro-mechanical systems and system architecture, along with associated documentation per established quality procedures. This individual will lead multidisciplinary teams to meet product and project requirements, collaborating with engineers from various companies and industries. In addition to systems engineering duties, this individual will serve as the Hardware Engineer on the project team and act as the technical liaison for the customer.</p><p><br></p><h2>Responsibilities</h2><ul><li>Serve as the primary technical contact for customers on projects.</li><li>Coordinate and facilitate interdisciplinary technical discussions within project teams.</li><li>Accountable for the technical project scope and effort.</li><li>Lead hardware engineering efforts on the project team.</li><li>Coordinate and document system-level analysis including system modeling, algorithm development, simulations, and system architecture.</li><li>Create and build internal requirement sets and assist the customer in developing user requirements when needed.</li><li>Support the development of risk management plans and reports.</li><li>Ensure product verification and validation, and ensure traceability is met for all requirements.</li><li>Perform and participate in technical design reviews during product realization.</li></ul><h2>Essential Skills</h2><ul><li>Bachelor&#39;s degree in Electrical Engineering or Computer Engineering.</li><li>Five or more years of experience, preferably in the medical device field, in systems engineering.</li><li>Five or more years developing electronic hardware in regulated environments with system designs compliant with IEC, ISO/EN, and IEC standards.</li><li>Substantial experience in Hardware Development prior to transitioning into a systems role.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Master’s Degree in Engineering is a plus.</li><li>Experience with requirements management tools is a plus.</li><li>Experience with modeling tools such as Matlab and Simulink is a plus.</li><li>Knowledge of FDA 510(k), PMA, and De Novo pre-market submission processes is a plus.</li><li>Experience developing Class II and III medical devices is a plus.</li></ul>

Senior Systems Engineer

<h1><strong>Job Title: Principal Systems Engineer</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a skilled Principal Systems Engineer who will play a crucial role in the design and development of defense systems, ensuring they meet stringent specifications and performance requirements. This position requires a strong <span style="color: rgb(8, 7, 7); background-color: none;">background</span> in systems engineering and a keen understanding of defense industry standards. The ideal candidate will thrive in a fast-paced environment and work collaboratively with cross-functional teams.</p><p><br></p><h2>Responsibilities</h2><ul><li>Support the logical and systematic conversion of customer or product requirements into total systems solutions, considering technical, schedule, and cost constraints.</li><li>Perform functional analysis, timeline analysis, detail trade studies, requirements allocation, and interface definition studies to translate customer requirements into hardware and software specifications.</li><li>Troubleshoot and resolve system issues, collaborating with cross-functional teams to identify root causes and implement solutions.</li><li>Deliver technical guidance and recommendations to the engineering team, driving innovation and advanced prototype concepts in automation, modeling and simulation, software architectures, and integration outcomes.</li><li>Conduct system integration and testing to verify and validate the functionality, performance, and security of defense systems.</li><li>Participate in, lead, and coordinate preparation, conduct, and closeout of internal and external customer reviews, including SRR, PDR, CDR, TRR, and Stage Gate reviews.</li><li>Identify potential risks and costs associated with system development and implementation.</li><li>Ensure compliance with defense industry standards and regulations.</li></ul><h2>Essential Skills</h2><ul><li><strong><em>12 + years of proven experience in systems engineering within the Defense Industry (Missile Systems or Weapons)</em></strong></li><li>Strong <span style="color: rgb(8, 7, 7); background-color: none;">background</span> in systems engineering.</li><li>Ability to manage and collaborate across cross-discipline teams (Electrical, Mechanical, Software, GNC, Manufacturing, Operations, etc.).</li><li>Intermediate experience in MS Word, MS Excel, MS Visio, MS Project, and/or other applicable tools.</li><li>Integration, test, verification, and validation experience.</li><li>Ability to generate block diagrams and interface control diagrams (electrical, logical, software, etc.).</li><li>Ability to obtain necessary security clearances.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s degree in engineering or a related field preferred.</li><li>Desired - Model-based engineering and tools (MBSE, SysML, or equivalent).</li><li>Desired - Configuration management experience.</li><li>Rapid development skills.</li><li>Requirements development, management, and requirements configuration control.</li></ul><h2>Work Environment</h2><p>The work environment consists of office, research and development, test, and small manufacturing settings. The company offers an industry-leading position in GPS/PNT, with a small company feel and vibe. This is a permanent position with negotiable PTO and holiday benefits.</p>

<h1><strong>Job Title: Sr Systems Engineering Analyst</strong></h1><p><br></p><h2>Job Description</h2><p>As a member of the MDA MASC-F team, you will contribute to the development and qualification of missile defense system hardware and software. This role involves supporting the Modeling and Simulation Contract – Framework and Tools (MASC-F), which ensures readiness against evolving threats through system assessments, engagement conditions, and target phenomena evaluations.</p><p><br></p><h2>Responsibilities</h2><ul><li>Support the development and qualification of missile defense system hardware and software.</li><li>Evaluate system configurations, engagement conditions, and target phenomena.</li><li>Run &#39;what-if&#39; scenarios to ensure effective system configurations.</li><li>Provide products and tools to support modeling and simulation enterprise.</li><li>Assess operational effectiveness and survivability through critical data analysis.</li><li>Integrate real-world hardware and constructive models into one accurate system.</li><li>Evaluate fielded and conceptual architectures against various threats.</li></ul><h2>Essential Skills</h2><ul><li>Experience with Red Hat Enterprise Linux OS.</li><li>Proficiency in Python or similar technology.</li><li>Exposure to MDA system technology.</li><li>Secret security clearance to start.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Interface experience with phenomenology knowledge.</li><li>Technical-depth knowledge with at least one sensor (RF or EOIR).</li><li>Ability to deliver technical briefings at high levels.</li><li>Understanding of 6-DOF trajectory analysis.</li><li>Real-time understanding of blocking calls and semaphore impacts.</li><li>Knowledge of TCP/IP and Unicast.</li><li>Core Truth Model experience is a plus.</li></ul><h2>Work Environment</h2><p>The work will be performed onsite in Huntsville, AL, with the option of a 9/80 schedule. A government security clearance of SECRET or higher is required</p>

Senior Systems Engineering Analyst

<h1><strong>Job Title: Technical Writer</strong></h1><p><br></p><h2>Job Description</h2><p>Collaborate with various teams to capture technical information and transcribe it into clear documentation for internal and external use in a medical device environment.</p><p><br></p><h2>Responsibilities</h2><ul><li>Distill technical information into accessible documentation.</li><li>Support the formatting and proofreading of the Design History File (DHF) for the generator New Product Introduction (NPI).</li><li>Work with software architecture documents, operator manuals, and labeling instructions.</li><li>Comprehend and document embedded and firmware medical device products.</li><li>Develop trace matrixes and upstream documentation.</li><li>Support new contract manufacturers by writing and releasing design change orders.</li><li>Provide oversight on proper documentation for regulatory submissions.</li></ul><h2>Essential Skills</h2><ul><li>Medical device experience and understanding of an ISO13485 environment.</li><li>Proficiency in technical writing, specifically within medical devices.</li><li>Experience with DHF, firmware, change orders, quality inspection plans, regulatory submissions, and design control.</li><li>Experience working with complex products such as electromechanical devices, robotics, generators, and diagnostics/biotech.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with Verge Quality Management System (QMS) is a plus.</li><li>Quality Experience <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">background</span></span> is preferred.</li><li>5 years of professional experience in a medical device environment.</li></ul><h2>Work Environment</h2><p>The role initially requires working Monday through Friday from 9am to 5pm, transitioning to a hybrid model with 3 days on-site once performance is steady. Work in a state-of-the-art facility in Santa Clara, contributing to innovative electronic product development.</p>

Senior Technical Writer

<h1><strong>Job Title: Technical Writer</strong></h1><p><br></p><h2>Job Description</h2><p>Collaborate with various teams to capture technical information and transcribe it into clear documentation for internal and external use in a medical device environment.</p><p><br></p><h2>Responsibilities</h2><ul><li>Distill technical information into accessible documentation.</li><li>Support the formatting and proofreading of the Design History File (DHF) for the generator New Product Introduction (NPI).</li><li>Work with software architecture documents, operator manuals, and labeling instructions.</li><li>Comprehend and document embedded and firmware medical device products.</li><li>Develop trace matrixes and upstream documentation.</li><li>Support new contract manufacturers by writing and releasing design change orders.</li><li>Provide oversight on proper documentation for regulatory submissions.</li></ul><h2>Essential Skills</h2><ul><li>Medical device experience and understanding of an ISO13485 environment.</li><li>Proficiency in technical writing, specifically within medical devices.</li><li>Experience with DHF, firmware, change orders, quality inspection plans, regulatory submissions, and design control.</li><li>Experience working with complex products such as electromechanical devices, robotics, generators, and diagnostics/biotech.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with Verge Quality Management System (QMS) is a plus.</li><li>Quality Experience <span style="color: rgb(8, 7, 7); background-color: none;">background</span> is preferred.</li><li>5 years of professional experience in a medical device environment.</li></ul><h2>Work Environment</h2><p>The role initially requires working Monday through Friday from 9am to 5pm, transitioning to a hybrid model with 3 days on-site once performance is steady. Work in a state-of-the-art facility in Santa Clara, contributing to innovative electronic product development.</p>

<h1><strong>Job Title: Hardware Test Engineer</strong></h1><p><br></p><h2>Job Description</h2><p>As a member of the Verification and Validation engineering team, you will be responsible for supporting product verification, validation, and compliance test activities on electrical and mechanical medical device components and systems. Your expertise will be applied to all levels of product development, from prototype components to final system design. This role involves planning, developing, executing, and validating test methods, and creating associated documentation. You will interface with and support various groups, including R&amp;D, Project Management, Quality, and Manufacturing.</p><p><br></p><h2>Responsibilities</h2><ul><li>Develop and execute verification test methods, protocols, and reports for the verification of requirements on components and systems.</li><li>Drive quality into product development through analysis, testing, and timely feedback of test results to the cross-functional team.</li><li>Reverse engineer designs, review requirements, and fully understand design features to perform test impact assessments, create test strategy, and develop full test plans.</li><li>Design test cases including methodology, setups, materials, equipment, procedure, and acceptance criteria based on requirement and standard.</li><li>Conduct functional testing of mechanical assemblies, electrical circuits, and systems.</li><li>Serve as a key contributor to cross-functional team meetings and design reviews.</li><li>Review and analyze requirements and compliance standards as part of test development.</li><li>Support the hardware team in product development, concept feasibility, pre-compliance, and change activities by developing tests and providing test data.</li><li>Design hardware and/or software tools and fixtures for executing test methods and analyzing data.</li><li>Review, understand, and characterize electrical/mechanical designs to develop test methods ensuring requirement coverage.</li><li>Lead small teams through test projects for electromechanical components and systems.</li><li>Read and understand medical compliance standards and requirements, evaluate risks, and develop test procedures that ensure requirements are met, including leading test execution at third-party medical device safety test labs.</li></ul><h2>Essential Skills</h2><ul><li>3+ years of experience with electromechanical systems.</li><li>3+ years of experience conducting functional testing of hardware and software systems.</li><li>1+ year of experience in a regulated setting such as Medical, Automotive, or Defense.</li><li>Experience developing test procedures from requirements.</li><li>Bachelor’s degree in Electrical Engineering, Computer Engineering, or Biomedical Engineering.</li><li>Experience with test engineering and using test equipment such as oscilloscopes.</li><li>Experience with system and component level V&amp;V testing, plans, procedures, and reports.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience using electrical and mechanical lab equipment, such as oscilloscopes, DMM, power supplies, force/pressure gauges, calipers, thermometers, flow meters, and scales.</li><li>Experience with hardware test and validation procedures.</li></ul><h2>Work Environment</h2><p>This role is based in an office environment with a lab setting. You will work with large pieces of capital equipment, simulating end-user conditions. Testing will occur after software updates have been implemented.</p>

Senior Test Engineer

<h1 style="text-align: center;"><strong>Validation Engineer</strong></h1><p>The Validation Engineer will play a crucial role in commissioning and qualification efforts for equipment, utilities, and processes. This position requires consulting with site technical services for process and cleaning validation, while reporting to the Director of Manufacturing Engineering.</p><p><br></p><h2>Responsibilities</h2><ul><li>Lead all validation activities and maintain the validation master plan for the site.</li><li>Manage and/or lead the validation team in all CQV activities to meet site goals and timelines.</li><li>Create commissioning, qualification, and validation documentation, including user requirement specification, design qualification, protocols, and final summary reports.</li><li>Conduct commissioning, qualification, and validation according to approved corporate standards and protocols.</li><li>Collaborate with the system owner to define user requirements and establish an appropriate CQV strategy.</li><li>Support quality systems such as change control, deviations, CAPA, audits, quality metrics, and annual product reviews.</li></ul><h2>Essential Skills</h2><ul><li>Proven experience in pharmaceutical and biotech environments.</li><li>Expertise in validation testing and protocols.</li><li>Knowledge in process validation and equipment validation.</li><li>Excellent technical writing skills.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor&#39;s or Master&#39;s degree in a scientific discipline or related field.</li><li>Minimum of 5 years of experience in commissioning, qualification, and validation of cGMP or cGXP.</li><li>Specific knowledge of biological and pharmaceutical cGMPs (USDA and EU).</li><li>Strong verbal, written, interpersonal, organizational, and communication skills.</li></ul><h2><br></h2>

Senior Validation Engineer

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