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<h3>Job Description</h3>
Our client, a leading pharmaceutical company focused on discovering, developing, manufacturing, and commercializing therapeutic treatments is currently seeking a Senior Document Control Specialist to join their team for a 6-month contract (potential to extend). This person will be responsible for overseeing the management, organization, and maintenance of all controlled documents within the company’s quality management system (QMS), supporting the efficient operation of the pharmaceutical development and manufacturing processes.
 
Responsibilities:
 
 Document Management: 
<ul>
<li>Manage the lifecycle of controlled documents, including creation, revision, review, approval, distribution, and archival</li>
<li>Ensure documents are accessible, accurate, and up-to-date within the electronic document management system (EDMS).</li>
<li>Coordinate with cross-functional teams to ensure timely review and approval of documents. </li>
</ul>
 
 Compliance: 
<ul>
<li>Ensure all document control activities comply with current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP), and per company Procedures.</li>
<li>Maintain audit readiness by ensuring documents are in a state of compliance and available for internal and external audits. </li>
</ul>
 
 Process Improvement: 
<ul>
<li>Identify and implement process improvements to enhance the efficiency and effectiveness of the document control system.</li>
<li>Develop and maintain document control procedures, work instructions, and training materials. </li>
</ul>
 
 Training &amp; Support: 
<ul>
<li>Provide training and support to employees on document control processes</li>
<li>Act as a subject matter expert for document control during audits and inspections. </li>
</ul>
 
 Reporting &amp; Metrics: 
<ul>
<li>Generate and analyze document control metrics and reports to monitor performance and identify areas for improvement.</li>
<li>Present findings to management and recommend corrective actions as needed. </li>
</ul>
 
Qualifications
<ul>
<li>Bachelor’s degree in a related field (e.g., Life Sciences, Quality Assurance, or Regulatory Affairs) and a minimum of 5-7 years of experience in document control within the pharmaceutical, biotechnology, or medical device industry.</li>
<li>Strong knowledge of cGMP, GDP, and regulatory requirements (e.g., FDA, EMA).</li>
<li>Proficiency in using electronic document management systems and other relevant software.</li>
<li>Excellent organizational, communication, and interpersonal skills.</li>
<li>Ability to work independently and as part of a team in a fast-paced, dynamic environment.</li>
<li>Detail-oriented with a commitment to quality and accuracy.</li>
<li>Certification in Document Control or Quality Management preferred</li>
<li>Experience with lean or continuous improvement methodologies preferred</li>
<li>Familiarity with global regulatory requirements and international document control standards preferred</li>
</ul>
 
Salary: $45-55/hr
 
 
 If you are interested in this position, please send your resume to <a href="mailto:apowell@daleyaa.com" target="_blank">apowell@daleyaa.com</a>

Sr. Quality, Document Specialist

<h3>Job Description</h3>
About the job
 
Ailux is the biologics drug discovery division of XtalPi Inc., a global leader in AI drug discovery. By leveraging proprietary AI models and comprehensive wet-lab capabilities, Ailux partners with biotech and large pharmaceutical companies around the world to deliver highly differentiated drug candidates that meet unmet medical needs. 
We are seeking a highly motivated and experienced technical communications manager to join the Ailux communications team. You will leverage your scientific background and communication skills to craft compelling technical content and thought-leadership insights for targeted audience. With a growth mindset and strong interest in antibody drug discovery, you will play a pivotal role in refining our product strategy and elevating our brand reputation. 
 
Key Responsibilities
<ul>
<li>Collaborate seamlessly with R&amp;D, communications/branding, and BD team to create and deliver impactful technical content, including platform case studies, posters, white papars, flyers, and other multi-media contents</li>
<li>Create high-quality materials for BD opportunities, including platform partnership, research collaboration, and drug licensing </li>
<li>Conduct market research and strategic analysis to ensure technical contents remain competitive and relevant</li>
<li>Actively involved in internal development and product portfolio strategy</li>
<li>Promote brand awareness and thought leadership in major conferences</li>
</ul>
Qualifications
<ul>
<li>Ph.D. degree in biology, biotechnology, bioengineering, or a related field, with a minimum of 2 years of business experience in technical marketing, scientific communication, market research, consulting, or related functions within the life sciences industry. A Master's degree with highly relevant experience will be considered. </li>
<li>Extensive reserach or working experience in therapeutic drug discovery. A basic understanding of AI/ML is preferred.</li>
<li>Exceptional skills in scientific writing, visualization, and communication.</li>
<li>Experience in brand awareness and/or lead-generation campaigns.</li>
<li>Results-driven.</li>
<li>Strong intellectual curiosity and eagerness to acquire new knowledge and skills.</li>
</ul>

Technical Communications Manager

<h3>Job Description</h3>
The Principal Solution Architect will lead IT transformation efforts, including cloud adoption, AI solution development, and enterprise roadmaps. This role operates at the highest level of architectural leadership and will guide the entire solutions architecture function.
Responsibilities:
<ul>
<li>Define the long-term T architecture strategy and roadmaps.</li>
<li>Lead cloud migration and AI solution adoption across programs.</li>
<li>Evaluate vendors and participate in technology selection strategies.</li>
<li>Guide and mentor other architects (Lead + Senior Architects).</li>
<li>Partner with executives and stakeholders to drive large-scale transformation initiatives.</li>
</ul>
Qualifications:
<ul>
<li>15+ years of experience in IT architecture roles, with significant leadership responsibilities.</li>
<li>Proven track record leading cloud transformations and AI-driven initiatives.</li>
<li>Strong experience in solutions engineering and enterprise architecture.</li>
<li>Ability to influence at the executive level while staying hands-on in technical design.</li>
<li>Healthcare/Medicaid IT domain experience strongly preferred.</li>
</ul>

Principal Solution Architect

<h3>Job Description</h3>
Job Description
For more than 50 years, EdgeTech has been the industry leader in the design and manufacture of advanced underwater sonar systems for applications involving seabed survey, target detection, object identification, mooring instrumentation, and acoustic tracking/positioning.&nbsp; Our products are used to support a variety of customers, from offshore oil and gas to fisheries/science/underwater research, defense, and police/fire search and rescue
We’re looking for an engineer/scientist with interest in applying signal processing to develop algorithms that enable new capabilities in next-generation sonar systems. Typical assignments include algorithm design, analysis, and implementation; sonar system analysis; involvement in software and hardware prototyping and test activities; documentation and planning; as well as sea testing, data collection, and post-trial analysis.
Job Responsibilities
<ul>
<li>Design algorithms for processing of sonar signals including waveform design, beamforming, broadband processing, and detection.</li>
<li>Develop processing algorithms and assess their performance. Interpret results.</li>
<li>Collaborate with real-time code developers and modeling/simulation analysts to develop and integrate system software.</li>
<li>Develop simple and reliable signal processing algorithms for a variety of processors, to include ARM’s, SoC’s/SoM's and FPGAs</li>
<li>Assist with the development of signal processing specifications and their implementation</li>
<li>Test software, firmware and full sonar solutions in simulation, hardware-in-the-loop, and field demonstrations</li>
<li>Collaborate with a cross-functional team testing your contributions and analyzing performance</li>
<li>Support the engineering, production, and sales/marketing teams with productization of technologies and solutions</li>
<li>Understand broad product objectives to develop and maintain relationships with major customers.</li>
<li>Collaborate with other engineers, customers and the technical community to advance sonar capabilities for current and future applications</li>
</ul>
Job Requirements
<ul>
<li>This job can be filled at multiple levels, depending upon the successful candidate’s education and experience. Minimum education required is an M.S. degree in an engineering or science related discipline plus five year’s related experience or an equivalent combination of education and experience.</li>
<li>Experience with signal processing theory and applications</li>
<li>Experience with scripting and analysis tools such as Matlab and Python</li>
<li>Experience with planning and conducting sea trials and surveys.</li>
<li>Highly effective written and verbal communication skills</li>
<li>Ability to work effectively in a team and set priorities</li>
<li>Work with sonar imaging technologies or hydrographic applications is a big plus.</li>
<li>Familiarity with hardware (amplifiers, antennas/transducers, filters), and digital processing with FPGAs, GPUs, CPUs, is desirable but not required.</li>
<li>Work will include a mix of field and office assignments, with domestic and international travel as part of the job.</li>
</ul>
If interested, please contact:
Kevin Igo
<a href="mailto:Kevin.igo@edgetech.com" target="_blank">Kevin.igo@edgetech.com</a>
EdgeTech is an equal opportunity employer.
Company DescriptionEdgeTech is a leading manufacturer of underwater technology solutions. The company is known worldwide for its high quality products which include: side scan sonars, sub-bottom profilers, bathymetry systems, AUV and ROV-based sonar systems, combined and customized solutions. In addition to the full line of underwater survey products, EdgeTech provides reliable USBL systems, transponder beacons, deep sea acoustic releases, shallow water and long life acoustic releases, MRUs and customized underwater acoustic command and control systems. 
<h3>Company Description</h3>
EdgeTech is a leading manufacturer of underwater technology solutions. The company is known worldwide for its high quality products which include: side scan sonars, sub-bottom profilers, bathymetry systems, AUV and ROV-based sonar systems, combined and customized solutions. In addition to the full line of underwater survey products, EdgeTech provides reliable USBL systems, transponder beacons, deep sea acoustic releases, shallow water and long life acoustic releases, MRUs and customized underwater acoustic command and control systems.

Sonar System Engineer

<h3>Job Description</h3>
Third Pole is on a mission to expand the lifesaving benefits of Nitric Oxide inhalation therapy, making it accessible to millions of respiratory challenged newborns and adults around the world. This is a rare opportunity to be part of a rapidly growing team, making a huge social impact, touching the lives of those we love and care about most.
 
We are a fast-paced startup developing a game-changing technology that generates Nitric Oxide on demand, at the patient location, from the air we breathe. Our Third Pole community is grounded in the values of collaboration, embracing diverse ideas, commitment, and transparency without the politics found in most companies. Our motto is we are only successful if we all cross the finish line together! Sound like you?
 
The Principal Software Engineer provides expertise in the design, development, characterization, and testing of complex software/firmware used to drive and manage complex electromechanical medical devices. In this role you will interface with a strong multidisciplinary team across the full product development life cycle including requirements, risk, implementation and testing activities. This position is full-time onsite in Waltham, MA.
 
Responsibilities:
<ul>
<li>Collaboratively work with System’s Engineering to translate system level requirements into product architectures making tradeoff decisions regarding hardware and software partitioning</li>
<li>Uses modeling, hardware-in-the-loop simulation and actual devices to develop, debug and test complex systems to meet required performance</li>
<li>Develop software subsystem architectures aligned to product level requirements and architectures including software requirements definitions and sub-system designs</li>
<li>Design and develop software/firmware utilizing C and C++ on embedded real time operating systems (RTOS) following company and industry requirements and best practices</li>
<li>Performs advanced risk analyses using FMEA and fault tree methods. Works with other engineering disciplines to develop, implement, and verify solutions</li>
<li>Perform software verification including code reviews, writing unit test cases, and running static analysis</li>
<li>Document system design inputs and outputs using the Third Pole’s design control and document management system</li>
<li>Evaluates product performance on an on-going basis and initiates and evaluates required changes to the designs to improve and optimize performance</li>
<li>Solve complex software issues by analyzing critical factors and recommending corrective or alternative actions</li>
<li>Ensures adherence to company quality system, product specifications, industry standards, and quality and regulatory procedures and requirements</li>
<li>Maintains accurate documentation of concepts, designs, drawings, and processes through lab notebooks or other methods</li>
</ul>
 
Requirements:
<ul>
<li>Bachelor’s Degree in Software or Electrical Engineering. Master’s degree preferred.</li>
<li>10+ years Software Engineering experience in the design and development of complex, real time software driven electromechanical Class II medical devices in C and C++; Class III experience preferred</li>
<li>Detailed knowledge of key regulatory requirements included ISO 13485, ISO 14971, ISO 62304 as well as FDA QSR 21 CFR Part 820</li>
<li>Recent microcontroller experience</li>
<li>Experience with electronic design control and document management systems preferred</li>
<li>Ability to work independently with high competency and little guidance.</li>
<li>Must be a creative problem solver that can think outside of the box to develop novel solutions to complex problems</li>
<li>Must be able to work in a fast paced, high energy, collaborative team that possesses a strong sense of urgency</li>
<li>Strong design control and documentation skills</li>
<li>Strong analytical and leadership skills</li>
</ul>
 
Third Pole, Inc. provides equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law.

Principal Algorithms & Embedded Software Engineer

<h3>Job Description</h3>
Job Description
Hybrid Office Schedule - 3 days in office in Ayer, MA 
No Sponsorship - Must have US Citizenship or Green Card 
We are seeking a Senior Digital Transformation Engineer for our client's manufacturing company in Ayer, MA. This role leads strategic initiatives that align technology with business goals, driving the transition to modern digital systems and scalable solutions that enhance efficiency, automation, and customer experience.
Responsibilities
<ul>
<li>Lead enterprise-level digital projects including ERP, order management, fulfillment, eCommerce, and platform integrations</li>
<li>Develop, mentor, and guide software developers and digital transformation engineers</li>
<li>Serve as an internal consultant to identify process gaps and implement scalable, automated digital solutions</li>
<li>Manage external vendors and offshore development teams; ensure project timelines and quality standards are met</li>
<li>Write and maintain Python scripts (Pandas, NumPy) to automate data workflows, API integrations, and reporting</li>
<li>Partner with Finance and Operations to build data reports, reconcile inventory, and optimize analytics</li>
<li>Evaluate technology vendors (ERP, MES, CMMS, B2B/B2C, analytics, personalization, etc.) and make recommendations</li>
<li>Build business cases with ROI analysis to support digital investment decisions</li>
<li>Oversee multiple company websites, domains, and analytics tools while ensuring GDPR/CCPA compliance</li>
<li>Collaborate with IT and Help Desk partners to document infrastructure and ensure business continuity</li>
</ul>
 
MUST HAVES:
<ul>
<li>Bachelors degree in Computer Science, Software Engineering, Information Technology, or a related technical field</li>
<li>6+ years of experience in digital strategy, customer experience, or business operations</li>
<li>Proven ability to leverage digital technologies to drive efficiency, innovation, and process improvement</li>
<li>Hands-on experience developing, debugging, and implementing software solutions, including Python (Pandas, NumPy).</li>
<li>Experience leading MVP builds, defining technical architecture, and managing vendor or client relationships.</li>
<li>Skilled in building business cases and performing ROI analysis to support technology investments.</li>
</ul>
This is a hybrid position with 3 days in office in Ayer, MA.

Senior Digital Transformation Engineer

<h3>Job Description</h3>
Principal Systems Engineer
Location: Andover, MA (In-person)
 
Company Overview
Digital Health Solutions (DHS) is a premier consulting firm dedicated to advancing medical device innovation. We partner with companies across the medical technology spectrum to deliver safe, effective, and compliant solutions. With deep expertise in IEC 62304, ISO 13485, and FDA/EU regulatory frameworks, DHS helps clients accelerate product development while ensuring patient safety and clinical impact remain at the core. Our mission is simple yet powerful: to guide the development of medical technologies that improve and save lives.
 
Position Overview
We are seeking an accomplished Principal Systems Engineer to join our growing team. This role is ideal for a highly experienced systems thinker who thrives at the intersection of engineering, clinical application, and regulatory compliance. The Principal Systems Engineer will lead complex projects across Class II and III medical devices, bringing together cross-functional teams to deliver innovative solutions in areas such as neurostimulation, cardiac support, and medical imaging.
At DHS, you won’t just contribute technical, you will shape strategy, mentor emerging engineers, and influence the next generation of patient-focused technology. This is a hands-on leadership role where you’ll translate clinical needs into actionable requirements, architect and validate systems, and drive design control excellence from concept through commercialization.
We are looking for a candidate who combines technical depth, regulatory fluency, and leadership presence. The ideal candidate is someone who can balance innovation with compliance, build consensus across diverse stakeholders, and drive projects to successful completion in fast-paced environments.
 
Key Responsibilities
<ul>
<li>Lead systems engineering activities across the full product lifecycle, from concept through verification, validation, and commercialization.</li>
<li>Translate user and clinical needs into system, subsystem, and component requirements while maintaining rigorous traceability.</li>
<li>Participate in hardware and software design and development activities, working with engineers to ensure the design will meet requirements.</li>
<li>Ensure requirements can be verified in compliance with design controls and other QMS SOPs.</li>
<li>Architect system-level solutions, define interfaces, and guide trade-off analyses to achieve optimal design outcomes.</li>
<li>Oversee risk management activities (HA, FMEA, risk-benefit analysis) ensuring compliance with ISO 14971 and related standards.</li>
<li>Direct verification and validation strategies, author test protocols/reports, and coordinate testing with external labs.</li>
<li>Drive design control documentation and ensure adherence to ISO 13485, IEC 60601, IEC 62304, and FDA/EU regulations.</li>
<li>Collaborate cross-functionally with clinical, quality, regulatory, and manufacturing teams to resolve conflicts and ensure alignment.</li>
<li>Mentor junior engineers, fostering professional growth and building DHS’s technical leadership bench.</li>
<li>Contribute to program management activities including project planning, deliverable tracking, and executive reporting.</li>
<li>Support business development efforts through technical input to proposals, client engagement, and thought leadership.</li>
</ul>
 
Preferred Qualifications
<ul>
<li>Master’s degree in Biomedical, Electrical, Systems, or related Engineering field (PhD a plus).</li>
<li>10+ years of experience in systems engineering within Class II/III medical devices.</li>
<li>Proven track record in requirements management, system architecture, and verification/validation.</li>
<li>Strong knowledge of regulatory compliance (FDA 21 CFR Part 11/820, EU MDR, ISO 13485, IEC 60601, IEC 62304, ISO 14971).</li>
<li>Experience leading cross-functional teams, managing CAPAs, and closing complex regulatory gaps.</li>
<li>Skilled in tools such as JIRA, Confluence, and test management platforms.</li>
<li>Strong interpersonal skills with the ability to communicate effectively across technical and non-technical audiences.</li>
</ul>
 
What We Offer
<ul>
<li>Competitive salary and benefits package, including health insurance, 401(k) plan with employer match, vision, dental and paid time off.</li>
<li>The opportunity to work on cutting-edge medical technologies that directly improve patient lives.</li>
<li>Exposure to a broad range of projects and modalities, from implantable devices to advanced imaging systems.</li>
<li>Mentorship and collaboration with leading experts in systems engineering, regulatory affairs, and product development.</li>
<li>A role where your technical leadership and strategic insight shape both client success and DHS’s growth.</li>
<li>The satisfaction of delivering solutions that balance innovation, compliance, and patient safety—making a tangible impact in healthcare.</li>
</ul>

Principal Systems Engineer

<h3>Job Description</h3>
We are seeking an experienced Cloud Engineer to join our engineering team and help design, implement, optimize, and maintain scalable cloud-based solutions. In this role, you will work closely with development and operations teams to ensure reliable and secure cloud infrastructure, streamline deployment processes, and guide teams on cloud best practices and new initiatives.
A successful candidate will be a proactive problem-solver with strong technical expertise in AWS and a collaborative approach to delivering efficient and secure cloud environments.
Key Responsibilities:
<ul>
<li>
Collaborate with engineering and development teams to evaluate and identify optimal cloud solutions.
</li>
<li>
Design, develop, automate, and deploy modular and scalable cloud-based systems.
</li>
<li>
Ensure the efficient operation and security of cloud infrastructure in compliance with company policies and industry best practices.
</li>
<li>
Identify, analyze, and resolve issues related to application deployment and cloud performance.
</li>
<li>
Regularly review existing systems and recommend improvements for scalability, performance, and security.
</li>
<li>
Provide cloud support and technical guidance to internal teams based on evolving business needs.
</li>
</ul>
Qualifications:
<ul>
<li>
Bachelor’s degree in computer science, Engineering, Mathematics, or a related field.
</li>
<li>
Minimum of 5 years of hands-on experience in cloud design, development, and deployment.
</li>
<li>
Proven experience leading enhancements and implementations on AWS cloud platforms.
</li>
<li>
Deep expertise in AWS services, tools, and architecture best practices.
</li>
<li>
Strong troubleshooting, analytical, and problem-solving skills.
</li>
<li>
Excellent communication and teamwork abilities.
</li>
<li>
Ability to stay current with emerging cloud technologies and industry trends.
</li>
</ul>
What We Offer:
<ul>
<li>
A collaborative and innovative environment where your expertise will shape scalable and secure cloud solutions.
</li>
<li>
Opportunities for professional growth and continued learning in cloud engineering and architecture.
</li>
</ul>

Cloud Engineer 3 / AWS / Onsite / Webster, MA

<h3>Job Description</h3>
Overview: \nWe’re seeking an experienced AWS Architect to join our team and lead the design, implementation, and optimization of cloud solutions on Amazon Web Services. This role will be responsible for translating business needs into secure, scalable, and reliable cloud architectures while providing technical leadership and guidance across teams. The ideal candidate will have deep AWS expertise, strong leadership skills, and a passion for innovation in cloud technologies.
Key Responsibilities:
<ul>
<li>
Design and implement end-to-end cloud architectures aligned with business goals.
</li>
<li>
Lead cloud migration projects from on-premises environments to AWS.
</li>
<li>
Ensure security, scalability, and high performance across all cloud systems.
</li>
<li>
Optimize cloud infrastructure for efficiency and cost-effectiveness.
</li>
<li>
Provide expert guidance on AWS services, best practices, and emerging technologies.
</li>
<li>
Mentor and support technical teams to strengthen AWS knowledge and architectural capabilities.
</li>
</ul>
Qualifications:
<ul>
<li>
Bachelor’s degree in computer science, Information Technology, or a related field.
</li>
<li>
10+ years of experience in IT or software development, including hands-on AWS architecture experience.
</li>
<li>
Proven track record in designing and deploying AWS solutions at scale.
</li>
<li>
Strong understanding of AWS computer, networking, storage, and security services.
</li>
<li>
Experience with Infrastructure as Code (Terraform, CloudFormation, or Ansible) and scripting (Python or Shell).
</li>
<li>
Excellent problem-solving, communication, and collaboration skills.
</li>
</ul>
Why Join Us:
<ul>
<li>
Work on impactful, large-scale cloud transformation projects.
</li>
<li>
Collaborate with talented teams and drive innovative AWS solutions.
</li>
<li>
Enjoy a supportive environment that values growth, creativity, and technical excellence.
</li>
</ul>

Cloud Architect / DevOps / Onsite / Webster, MA

<h3>Job Description</h3>
Job Title: Senior Software Engineer – Medical Devices 
Location: Andover, MA; 
 
Company Overview:
At Digital Health Solutions, we specialize in developing and supporting next-generation medical technologies — from embedded systems and connected mobile apps to cloud platforms, regulatory strategy, and contract manufacturing. As an ISO 13485-certified partner, we work with innovators building Class I–III medical devices, SaMD, and connected digital health solutions.
We are looking for a Senior Software Engineer to support our growing portfolio of medical device software projects. This is a hands-on role for someone who enjoys building secure, scalable systems across both cloud and mobile platforms and is comfortable working within a regulated product development environment.
 
Responsibilities:
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Design, develop, and maintain cloud-based services and APIs using C#/.NET and Azure
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Build and support React-based frontends for clinician and patient-facing applications
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Develop and maintain native Android applications in Java, integrating with BLE-connected medical devices and cloud services
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Work closely with firmware, systems, QA, and regulatory teams to ensure software meets medical device quality and compliance standards
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Participate in code reviews, design discussions, and SDLC documentation including risk control, architecture, and verification support for FDA submissions
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Follow best practices for cybersecurity, authentication, and privacy, aligned with HIPAA and FDA guidance
Required Qualifications:
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Minimum 5 years of professional software engineering experience
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Minimum 3 years of hands-on experience with cloud development using C#, .NET, React, and Azure
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Minimum 2 years of experience developing native Android apps in Java
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Experience working in regulated industries such as medical devices, healthcare, or life sciences
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Strong understanding of REST APIs, CI/CD pipelines, Git, and cloud security principles
Nice to Have
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Familiarity with FDA regulations, IEC 62304, or ISO 13485
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Experience with Bluetooth Low Energy (BLE) or connected health devices
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Exposure to tools like Jira, GitHub, Azure DevOps, or document automation systems used in FDA submissions
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Prior experience in consulting or multi-client environments
What We Offer:
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Competitive salary and benefits package, including health insurance, 401(k) plan with employer match, vision, dental and paid time off.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Opportunity to work with cutting-edge technology in the medical device industry.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;A supportive, collaborative work environment that fosters professional growth and development.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;The chance to make a meaningful impact on the safety and effectiveness of medical devices, ultimately improving patients' lives.

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