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<h3>Job Description</h3>
Job Description
Job Title: Senior Project Manager / Project Manager (K-12)
Location: Florida (Miami | Ft Lauderdale | West Palm Beach | Orlando)
Job Description:We are seeking an experienced Project Manager to oversee the financial, technical, and operational success of construction projects. The role involves managing all phases of project planning and execution, ensuring compliance with company policies and client expectations. The Project Manager will lead the project team, manage resources, and drive performance to achieve project goals.
Requirements:
<ul>
<li>Education: Bachelor’s degree in Construction Management, Civil Engineering, or a related field preferred.</li>
<li>Experience: 5-10 years in project management within the construction industry, particularly with large-scale or commercial projects.</li>
<li>Skills:
<ul>
<li>Proficient in industry-standard software (e.g., Vista, Procore, Microsoft Project, Bluebeam, Textura, OPEX).</li>
<li>Strong leadership, financial management, and problem-solving capabilities.</li>
<li>Excellent communication and team management skills.</li>
<li>Ability to oversee technical and operational project aspects, ensuring safety and quality compliance.</li>
</ul>
</li>
<li>Certifications:
<ul>
<li>PMP (Project Management Professional) certification preferred.</li>
<li>OSHA 30-Hour certification required.</li>
</ul>
</li>
</ul>
Key Responsibilities:
<ul>
<li>Leadership &amp; Team Development: Lead and develop the project team, promoting accountability and teamwork.</li>
<li>Project Planning &amp; Execution: Participate in pre-construction activities, manage schedules, oversee logistics, and lead the buy-out phase.</li>
<li>Document Control &amp; Risk Management: Manage project documents and proactively address risks.</li>
<li>Cost Control: Implement cost control measures, forecast financials, manage change orders, and oversee pay applications.</li>
<li>Quality, Safety &amp; Compliance: Ensure adherence to safety and quality standards throughout the project.</li>
<li>Client &amp; Stakeholder Management: Manage relationships with clients and stakeholders, lead OAC meetings, and ensure timely communication.</li>
<li>Project Closeout &amp; Post-Project Review: Ensure efficient project closeout and conduct post-project reviews for continuous improvement.</li>
<li>Business Development: Support business development initiatives and represent the company at industry events.</li>
</ul>

Senior Project Manger / Project Manager

<h3>Job Description</h3>
Job DescriptionDEKA Research &amp; Development is seeking a Software Engineer Co-Op&nbsp;to join our Software team for Fall 2025. This position will give exposure to several different aspects of software development including test automation, hands on trouble shooting, implementation based on software requirements and working on a product that directly improves user’s lives. DEKA offers Internships and Co-Ops for full time students* (must be at least 18 years of age). Applicants must be available&nbsp;for a 4-6 month&nbsp;Co-Op from July/August 2025 to December 2025. How you will make an impact as a Software Engineer Co-Op:
<ul>
<li>Use software engineering knowledge to solve issues found in embedded and test software</li>
<li>Improve DevSecOps via automated testing in CI/CD pipelines.</li>
<li>Conduct through investigation and code debugging</li>
<li>Perform verification and validation activities using automated software testing and test fixtures</li>
<li>Support development of software</li>
<li>Learn software processes</li>
</ul>
To be successful in this role as a Software Engineer Co-Op, you need the following skills and experience:
<ul>
<li>Must be currently enrolled in an undergraduate Computer Science, Software Engineering or equivalent program</li>
<li>Must have C++ programming experience&nbsp;</li>
<li>Python programming experience a plus</li>
<li>Have successfully completed at least one year of programming course(s)</li>
<li>Must be a self-starter eager to contribute in a team environment</li>
<li>Must have excellent verbal and written communication skills</li>
<li>Must be detail oriented</li>
</ul>
About DEKA:
One hour from the beach, Boston, and the mountains, the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research and Development, where we are taking the same innovation and cutting-edge technology into the modern age.
Behind DEKA’s brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering, design, and manufacturing. Here at DEKA, some of the most innovative and life-changing products of our time are created, and new ideas are always welcome and explored. Additional Information:
*Applicants should be aware that short-term housing options in Manchester, NH are limited and that DEKA is not able to financially assist with housing.&nbsp;
Public transportation is available and routes/schedules can be found by visiting the Manchester Transit Authority website,&nbsp;<a href="http://www.mtabus.org" target="_blank">www.mtabus.org</a>.
Please be aware that we try to make sure that our internship/Co-Op opportunities are well defined and will provide a unique experience. We understand that most candidates would like to know if they have a placement as soon as possible, but at DEKA it takes more time than other companies at we review every application that is submitted.&nbsp; We will try to let you know as soon as we can, but encourage you to pursue other opportunities as well.
*A full time student is defined as being enrolled in a minimum of 12 credits per semester at an undergraduate program, or a minimum of 9 credits per semester for a graduate program.
 &nbsp;
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Software Engineer Co-Op- Fall 2025

<h3>Job Description</h3>
Job Description
"All candidates must be directly contracted by ASK Consulting on their payroll and cannot be subcontracted. We are unable to provide sponsorship at this moment".
Job Title: CSV Analytical and Enterprise Validation Specialist
Location: Portsmouth, NH (03801)
Duration: 12 months
Pay rate: $66 hr on W2 AI
Job Description:
<ul>
<li>CSV, Analytical and Enterprise Validation specialist IV will lead validation activities including, but not limited to, software updates, new system introduction, Administration of systems and applications, and decommissioning activities as appropriate. This person will work closely with other functional groups like Manufacturing, Operations Technology, Computer System Validation, Engineering, and Quality Assurance to support updates to help the site remain in compliance and contribute to quality, on-time delivery and right first-time performance.</li>
<li>Provide Subject Matter Expert support to Quality Control, Manufacturing and other departments for the design, operation and troubleshooting of CSV, analytical and enterprise systems/applications.</li>
<li>Review and Approval of Installation Qualifications/Operational Qualifications and drafting Performance Qualifications as required.</li>
<li>Assist in generating User Requirements Specification Documentation, Electronic Records/Electronic Signatures, Data Integrity Risk Assessments and Audit Trail Risk Assessments.</li>
<li>Prepare Administration and Configuration specification document with support from vendor user manual.</li>
<li>Procurement of Analytical Equipment which includes ensuring system meets specifications, quotes, budgets and installations.</li>
<li>Performs user and application software administration on Enterprise systems. Works on troubleshooting assignments that are complex in nature where considerable judgment and initiative are required in making creative and effective recommendations to solve problems.</li>
<li>Create and or Revise SOPs for CSV, Analytical and enterprise systems and applications.</li>
<li>Participate on Risk Assessments</li>
<li>Review/Approve Commissioning Qualification Validation Documents</li>
<li>Perform other duties as assigned.</li>
</ul>
Education: Bachelor of Science - Science related discipline or relevant experience in the field Experience 5-10 Years
About ASK:&nbsp;ASK Consulting is an award-winning technology and professional services recruiting firm servicing Fortune 500 organizations nationally. With 5 nationwide offices, two global delivery centers, and employees in 42 states-ASK Consulting connects people with amazing opportunities
ASK Consulting is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all associates.

CSV Analytical and Enterprise Validation Specialist (263330)

<h3>Job Description</h3>
Job DescriptionWilcox Industries is looking for passion people who are excited to enable warfighters with leading edge tactical solutions. We currently have an opening for a full-time Quality Assurance Engineer (QE). This is an on-site position.&nbsp; This position is responsible for guiding efforts to identify and manage risks that could adversely affect plant or manufacturing business operations.&nbsp; This broad primary role includes loss elimination, risk management, and life cycle management. Roles and Responsibilities
<ul>
<li>Support the Quality Management Systems.</li>
<li>Formulates or helps to formulate Quality Assurance policies and procedures.</li>
<li>Perform internal audits, generate audit reports, and communicate results.</li>
<li>Designs and evaluates quality assurance processes, sampling systems, procedures, and statistical techniques. </li>
<li>Works with Engineering on new products development to establish standards, testing and acceptance criteria. </li>
<li>Designs or specifies inspection and testing mechanisms and equipment; analyzes production and service limitations and standards. </li>
<li>Conducts training on quality assurance concepts, and tools.</li>
<li>Evaluates, recommends, and facilitates lean activities for process improvement.</li>
<li>Collects, organizes, monitors, and distributes information related to quality and process improvement functions, including but not limited to compliance to and documentation of quality management standards. </li>
<li>Generates and analyze reports; distributes those reports to various users in the organization, customers and/or suppliers.</li>
<li>Perform other duties as necessary when directed to do so to support business needs. &nbsp;</li>
</ul>
Qualifications and Requirements
<ul>
<li>Bachelor’s Degree in Science or related work experience plus 2+ years’ experience in quality, production management, engineering, or operations or a combination of education and experience. </li>
<li>Background in Defense Industry a plus.</li>
<li>Regular on-site attendance is a necessary function of this position. </li>
<li>Ability to develop and manage good working relationships with internal departments (production, sales, logistics, accounting), contractors, suppliers inspectors and customers.</li>
<li>Experience with ISO 9100: 2015 a plus</li>
<li>Strong written and verbal communication skills.</li>
<li>High attention to detail and excellent time management skills.</li>
<li>Ability to identify issues and provide recommendations.</li>
<li>Ability to work independently and as part of a team.&nbsp; Meet daily, weekly and monthly deadlines. </li>
</ul>
 **Compensation offered may vary depending upon job-related knowledge, skills, and experience.&nbsp;&nbsp; Wilcox provides equal employment opportunity to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities LINKED&nbsp;
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QA Engineer - Optical

<h3>Job Description</h3>
Job DescriptionLooking for an experienced Product Safety Engineer to evaluate medical devices within our Product Safety Lab. The lab has full capability to test to the IEC 60601-1 and its related collateral standards. There is internal EMC capability as well. This person will support device design teams during concept and development with technical input and preliminary testing. Towards the end of development IEC 60601 TRFs will need to be generated for inclusion in an FDA 510k submittal.How you will make an impact as a Product Safety Test Engineer:
<ul>
<li>Work closely with project teams to become familiar with the operation and intended use of the medical devices being evaluated</li>
<li>Collaborate with project teams to steer product designs and risk management approach toward standards compliance&nbsp;</li>
<li>Provide design support during all phases of development and recommend appropriate investigational testing and design changes</li>
<li>Understand and interpret safety standards as they apply to DEKA devices and communicate to the project team</li>
<li>Author/review test cases and compliance test reports</li>
<li>Work with project teams to determine applicable operating and configuration modes for evaluation and testing</li>
<li>Conduct testing using internal work instructions and test standards</li>
<li>Record test data using good documentation practices</li>
<li>Contribute to design failure investigations and root-cause analyses as needed, making recommendations for design changes needed for compliance</li>
<li>Coordinate and oversee testing with contract test laboratories</li>
<li>Participate in the continued improvement of the Product Safety Lab including better efficiency and the expansion into new standards and test methods</li>
<li>Keep current with the latest FDA Guidelines and standards as they apply to DEKA devices</li>
<li>Maintain test equipment, lab supplies and a clean workspace</li>
</ul>
Skills you will need to be successful: 
<ul>
<li>3+ years’ experience in a Test Engineer role with Product Safety- related experience preferred</li>
<li>1 – 2 years of experience in a laboratory setting</li>
<li>BS degree in electrical, biomedical, mechanical engineering or other relevant field</li>
<li>Experience with general lab equipment such as DMM, oscilloscopes, and power supplies</li>
<li>Ability to work as part of an interdisciplinary team</li>
<li>Self-motivated and able to self-prioritize</li>
<li>Ability to clearly communicate verbally and in writing</li>
</ul>
Preferred Skills:
<ul>
<li>Familiarity with IEC 60601 collateral and particular standards </li>
<li>Experience with Risk Management and ISO 14971</li>
<li>Proficiency in electrical circuit analysis with an understanding of transformers, insulation and power electronics</li>
<li>Experience with applying knowledge of industry standards such as IEC 62368-1, IEC 62133-2, and&nbsp; 61010-1</li>
<li>Experience with technical writing</li>
</ul>
About DEKA: One hour from the beach, Boston, and the mountains, the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research &amp; Development, where we are taking the same innovation and cutting-edge technology into the modern age. Behind DEKA’s brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering, design, and manufacturing. Here at DEKA, some of the most innovative and life-changing products of our time are created, and new ideas are always welcome and explored. &nbsp;
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Product Safety Test Engineer

<h3>Job Description</h3>
Job Description
About Sequel&nbsp;
Sequel Med Tech is an early-stage company developing the next generation of precision drug delivery devices in the diabetes space.&nbsp;
Job Overview&nbsp;
We are seeking a Salesforce System Engineer to serve as the technical lead and solution architect for our CRM platforms. This individual will own the system design, configuration standards, and technical implementation of Salesforce Health Cloud, Sales Cloud, and related solutions. As a key technical partner to the Salesforce Product Manager, you will translate business requirements into scalable, secure, and future-ready solutions.&nbsp;
You’ll collaborate with cross-functional teams (Commercial, Clinical Ops, Customer Support, Data/Integration, and IT Security), ensure platform performance, guide platform enhancements, and lead the technical delivery of a HIPAA-compliant CRM that supports our rapid growth.&nbsp;
This role blends architectural thinking, configuration expertise, integration design, and hands-on build.&nbsp;
Job Responsibilities and Essential Duties&nbsp;
Platform Architecture &amp; Design&nbsp;
<ul>
<li>Lead the system architecture and technical design of Salesforce Health Cloud and Sales Cloud solutions.&nbsp;</li>
<li>Define data models, object relationships, sharing rules, and platform integration patterns.&nbsp;</li>
<li>Ensure alignment between business goals, product roadmaps, and scalable system architecture.&nbsp;</li>
</ul>
Configuration &amp; Technical Implementation&nbsp;
<ul>
<li>Translate functional requirements into robust technical designs and declarative solutions.&nbsp;</li>
<li>Implement and optimize Flows, Process Builder, Custom Objects, Page Layouts, Validation Rules, and Permissions.&nbsp;</li>
<li>Review and guide Apex code and Lightning component development (via internal or external developers).&nbsp;</li>
</ul>
Integration &amp; Data Engineering Support&nbsp;
<ul>
<li>Partner with data and integration teams on APIs, ETL pipelines, and external data connections (e.g., Snowflake, S3, MuleSoft).&nbsp;</li>
<li>Design secure, scalable, and performant integration architectures between Salesforce and adjacent systems.&nbsp;</li>
</ul>
Release Management &amp; Change Control&nbsp;
<ul>
<li>Coordinate with the Product Manager to plan and execute platform releases, enhancements, and testing cycles.</li>
<li>Support change control processes including sandbox management, deployment automation, and documentation.&nbsp;</li>
<li>Identify and resolve deployment risks and cross-environment dependencies.&nbsp;</li>
</ul>
Compliance, Security &amp; Governance&nbsp;
<ul>
<li>Ensure the Salesforce environment adheres to HIPAA, FDA, and internal security and data retention requirements.&nbsp;</li>
<li>Partner with IT Security and Compliance to implement appropriate encryption, access controls, and audit logging.&nbsp;</li>
</ul>
Documentation &amp; Support&nbsp;
<ul>
<li>Create technical documentation for configurations, data models, and integrations.&nbsp;</li>
<li>Mentor admins or junior engineers, and support troubleshooting as a Tier 3 resource for Salesforce issues.&nbsp;</li>
</ul>
Minimum Requirements&nbsp;
<ul>
<li>Bachelor’s degree (4-year) in Computer Science, Engineering, Information Systems, or related technical discipline preferred, or equivalent combination of education and experience.&nbsp;&nbsp;</li>
<li>5+ years of experience as a Salesforce System Engineer, Technical Consultant, or Solution Architect.&nbsp;</li>
<li>3+ years working directly with Salesforce Health Cloud and/or Sales Cloud in regulated environments.&nbsp;</li>
<li>Active Salesforce certifications (e.g., Platform App Builder, Advanced Administrator, Data Architect, or Integration Architect) are strongly preferred.&nbsp;</li>
</ul>
Required Knowledge, Skills and Abilities&nbsp;
<ul>
<li>Deep understanding of Salesforce declarative tools (Flows, Permissions, Object Model, Profiles, Sharing Settings).&nbsp;</li>
<li>Experience integrating Salesforce with external platforms using REST/SOAP APIs, middleware, or file-based data loads.&nbsp;</li>
<li>Knowledge of Apex, SOQL, Lightning Web Components (LWC), and deployment tools (Change Sets, VS Code, DevOps Center, or CI/CD pipelines).&nbsp;</li>
<li>Familiarity with Salesforce Connect, External Objects, data sync strategies, and error handling.&nbsp;</li>
<li>Experience in designing and optimizing data models for both B2B and B2C use cases.&nbsp;</li>
<li>Strong working knowledge of HIPAA and data privacy standards.&nbsp;</li>
<li>Experience supporting technology in med-tech, healthcare, or other FDA-regulated domains preferred.&nbsp;</li>
<li>Strong systems thinking, documentation skills, and the ability to break down complex requirements.&nbsp;</li>
<li>Ability to collaborate effectively with business users, architects, and technical partners.&nbsp;</li>
<li>Comfortable in fast-paced environments where flexibility and initiative are key.&nbsp;</li>
<li>Proven track record managing cross-functional projects and facilitating workshops or requirement sessions.&nbsp;</li>
<li>Comfortable working in Agile environments and using tools like Jira or Aha! for backlog and roadmap management.&nbsp;</li>
<li>Ability to travel a few times a year to the Manchester, NH office.&nbsp;</li>
</ul>
Sequel Med Tech provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.&nbsp;
At Sequel, we believe that when you thrive, we thrive. That’s why we’ve designed a benefits package that’s as thoughtful as it is generous. From day one, you’re automatically enrolled in our 401k plan—no waiting, no worries—with a 6% company match and 100% immediate vesting. We prioritize your well-being, especially for our employees and their families living with diabetes, with capped out-of-pocket insulin costs and GLP-1 coverage across all plans. With multiple medical plans through Aetna, including a 100% company-paid high-deductible plan paired with employer HSA contributions, you can select what suits your needs. Additional benefits include vision and dental plans, employer-paid short-term disability, and voluntary options like accident and pet insurance.&nbsp;&nbsp;
Need time to relax and recharge? You’ll enjoy flexible PTO and generous paid holidays, all while being part of a culture that values hard work, fun, and support. We don’t just offer jobs—we offer careers that build futures. Join us, and let’s grow together!&nbsp;&nbsp;
Environmental/Safety/Physical Work Conditions&nbsp;
<ul>
<li>Ensures environmental consciousness and safe practices are exhibited in decisions&nbsp;</li>
<li>Use of computer and telephone equipment and other related office accessories/devices to complete assignments&nbsp;</li>
<li>May work extended hours during peak business cycles&nbsp;</li>
<li>Physical requirements such as lifting specific weights&nbsp;</li>
<li>Some travelling is expected&nbsp;</li>
</ul>
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Salesforce System Engineer (CRM & Health Cloud)

<h3>Job Description</h3>
Job Description
DEKA Research &amp; Development, located in Manchester, NH, is seeking a Senior Systems Validation Engineer to work in a dynamic medical device R&amp;D environment. This is a high visibility role with a&nbsp;direct impact on the success of our projects. It will be a great opportunity to work on some amazing projects that make a positive impact on the world. Do you want to make a difference with your work? At DEKA you can!
How you will make an impact:
<ul>
<li>Writing test plans, test procedures&nbsp;and other activities involving performance, durability, and reliability assessments</li>
<li>Understand device design and core technologies in order to inform test method development</li>
<li>Determining test coverage for revisions to design</li>
<li>Creating and evaluating test fixtures needed for product design verification</li>
<li>Contributing to design failure investigations that may impact Risk Assessment, Hazard Analysis, and FTAs</li>
<li>Participating and contributing toward regulatory and agency submissions</li>
<li>Authoring Quality Plans, Test Summaries, and other documents</li>
</ul>
What you need to be successful:
<ul>
<li>BS in Physics, Electrical, Mechanical and/or Biomedical Engineering</li>
<li>3+ years' experience testing&nbsp;electro-mechanical medical devices</li>
<li>Leadership and/or mentoring experience&nbsp;</li>
<li>Knowledge and deep understanding of engineering fundamentals</li>
<li>Capability to create and clearly explain team objectives and write procedures for others to follow</li>
<li>Demonstrated problem solving ability and techniques</li>
<li>Ability to work as part of an interdisciplinary team</li>
<li>Self-motivated and able to self-prioritize</li>
<li>Must have excellent verbal and written communication skills</li>
</ul>
Preferred skills and experience:&nbsp;
<ul>
<li>Knowledge of FDA&nbsp;Quality System Regulations (QSRs) and/or ISO&nbsp;13485, and other medical device industry experience</li>
<li>Experience with&nbsp;research, development, and product testing</li>
<li>Experience writing procedures for others to follow</li>
<li>Experience with data and failure analysis</li>
<li>Broad measurement instrument knowledge</li>
</ul>
About DEKA:
One hour from the beach, Boston, and the mountains, the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research and Development, where we are taking the same innovation and cutting-edge technology into the modern age.
Behind DEKA’s brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering, design, and manufacturing. Here at DEKA, some of the most innovative and life-changing products of our time are created, and new ideas are always welcome and explored.
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Senior Test Engineer

<h3>Job Description</h3>
Job DescriptionMerrimack Manufacturing is a&nbsp;medical device manufacturer located in the Manchester Millyard. We are a growing manufacturing company that&nbsp;will play a crucial part in bringing innovative and life changing products to life. Duties &amp; Responsibilities:&nbsp; As the Project Manager you will initially be responsible for managing tasks related to the implementation of a new ERP system within the organization. You will work with cross-functional teams in Quality, Engineering, Finance, Manufacturing and Materials to ensure compliance with all required standards and processes are implemented on time within the new system. How success is defined in this position:
<ul>
<li>This initial project will be measured through the successful rollout of the ERP system per the required timelines</li>
<li>Future projects will be measured through the product realization process and meet all manufacturing performance metrics – on-time, yield, throughput, product costs, etc</li>
<li>Lessons learned through each project are identified and read across to future projects</li>
</ul>
 Preferred skills and experience:
<ul>
<li>Recent experience in an ERP implementation program. Experience with ExactMAX and Epicore Kinetic are a strong plus</li>
<li>Recent experience in a medical device manufacturing environment would also be a strong plus</li>
<li>Ability to manage effectively cross-functional teams without direct authority</li>
<li>High proficiency utilizing project management software (i.e. MS Project) and continually refining systems to help identify best practices</li>
<li>Direct experience leading projects from initial concept through design and release while working to standardize launch processes</li>
<li>Prioritizes the success of the team above individual goals.&nbsp; Acknowledges personal weaknesses and willing to improve.</li>
<li>Bachelor’s Degree in a relevant field or suitable combination of education and experience</li>
</ul>
How you will make an impact long term:
<ul>
<li>Lead new product realizations with cross-functional technical teams to bring projects from design authority to release to manufacturing</li>
<li>Translate high-level project goals into individual tasks;&nbsp;working with both internal and external project stakeholders</li>
<li>Drive delivery of aggressive goals while managing project schedule, cost, and project objectives</li>
<li>Interface with design authority and manage relationships to ensure crisp communication and alignment of objectives</li>
<li>Drive day-to-day project activities including removing roadblocks, managing resource conflicts, upholding high-performance standards, and meeting commitments</li>
<li>Work to standardize and continuously improve the product realization process</li>
<li>Work closely with management team to provide project schedules, resolve roadblocks, and effectively escalate problems when they arise </li>
<li>Experience in the development and validation of complex electromechanical devices</li>
<li>Preferred experience with structured problem solving tools, such as 5-Why, A3, Six Sigma, etc.</li>
<li>Experience working directly with suppliers and/or customers</li>
</ul>
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ERP Specialized Project Manager

<h3>Job Description</h3>
Job Description
DEKA Research &amp; Development, located in Manchester, NH, is seeking a Senior Systems Engineer&nbsp;to join a&nbsp;multi-disciplinary team for a medical device product development program. This exciting&nbsp;opportunity as a Senior Systems Engineer at DEKA will have a direct impact on the overall success of the project for an innovative and life-changing product.&nbsp;
A day in the role of a Senior Systems Engineer:
<ul>
<li>Overall electro-mechanical system architecture design, system specifications and upper-level design descriptions</li>
<li>Defining critical interfaces between subsystems and leading subsystem team leads in the integration of sophisticated software-driven electro-mechanical devices to ensure proper system function</li>
<li>System level test strategy, test specifications and protocols</li>
<li>Hazards analysis, failure modes analysis and mitigation design</li>
<li>Supporting program management to drive design goals within the entire project team; design goals may include product cost, size, weight, durability, manufacturability, and serviceability, among others</li>
<li>Supporting the development of project plans by estimating the effort required to complete design tasks</li>
<li>Providing guidance to manufacturing process development including process development, PFMEA review, and manufacturing test criteria</li>
</ul>
What are we looking for in a Senior Systems Engineer?
<ul>
<li>MS/BS in Engineering with 5-10&nbsp;years' experience in electro-mechanical machine and/or product design</li>
<li>Demonstrated experience in new product development environments including embedded software, complex mechanical systems, and electronics (PLC a plus)</li>
<li>Demonstrated technical leadership skills</li>
<li>Demonstrated history of inventive solutions to technical problems</li>
<li>Experience with requirements definition and management for performance, standards compliance, and testing</li>
<li>Experience with innovative first-generation product development, preferably in the medical device market</li>
<li>Experience with product testing, experimental methods and statistical techniques</li>
<li>Knowledge of manufacturing processes a plus</li>
<li>Prior experience with disposable products a plus</li>
</ul>
About DEKA:
One hour from the beach, Boston, and the mountains, the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research and Development, where we are taking the same innovation and cutting-edge technology into the modern age.
Behind DEKA’s brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering, design, and manufacturing. Here at DEKA, some of the most innovative and life-changing products of our time are created, and new ideas are always welcome and explored.
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Senior Systems Engineer

<h3>Job Description</h3>
Job DescriptionCompany Description 
We work as trusted business partners and always strive to deliver the most value and highest return on investment for our clients. We are highly trained business professionals with strong understanding of clients need. We work closely with the leading staffing trade associations, training, and research organizations to ensure we are knowledgeable of the latest industry trends and technologies.
Job Description 
We are seeking a highly skilled Senior Test Engineer specializing in 5G Protocol Systems to join our team in Manchester, United States. As a key member of our Anritsu testing division, you will play a crucial role in ensuring the quality and reliability of our 5G protocol testing solutions.
<ul>
<li>Develop and execute comprehensive test plans for 5G protocol systems using Anritsu test equipment</li>
<li>Analyze and interpret complex test results to identify and resolve issues in 5G network protocols</li>
<li>Design and implement automated test scripts to improve efficiency and coverage of testing processes</li>
<li>Collaborate with cross-functional teams to troubleshoot and debug system-level issues</li>
<li>Stay up-to-date with the latest 5G technologies and 3GPP specifications</li>
<li>Contribute to the development of new test methodologies and tools for emerging 5G features</li>
<li>Prepare detailed technical reports and documentation on test results and procedures</li>
<li>Mentor junior engineers and provide technical guidance on 5G protocol testing</li>
<li>Participate in industry forums and standards meetings to represent the company's interests in 5G testing.</li>
<li>5+ years of experience in wireless telecommunications testing, with a focus on 5G and LTE technologies</li>
<li>Proven expertise in 5G protocol testing and familiarity with Anritsu test equipment</li>
<li>Strong knowledge of wireless communication protocols and 5G network architecture</li>
<li>Proficiency in programming languages such as Python and C++</li>
<li>Experience with network simulation tools and protocol conformance testing</li>
<li>In-depth understanding of 3GPP specifications and standards</li>
<li>Excellent analytical and problem-solving skills with a detail-oriented approach</li>
<li>Strong debugging abilities and experience in troubleshooting complex system issues</li>
<li>Effective communication skills and ability to work collaboratively in a team environment</li>
<li>Relevant certifications in 5G technologies are preferred</li>
<li>Willingness to travel occasionally for on-site testing or industry events</li>
</ul>
Regards,
Mohammed ilyas,
PH - 229-264-4024 or Text - 229-469-1455 or You can share the updated resume at Mohammed@vtekis. com
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