Andover, MA

Engineer Jobs in Andover, MA

4 jobs found

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14d ago

Staff Software Engineer

Draeger Medical Systems, Inc. Andover, MA

Andover, MA

14d ago

$178k - $178k/yr Full time Backend Developer Integration Java Language

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Job Description

Draeger Medical Systems, Inc. is seeking a Staff Software Engineer in Andover, MA on a hybrid schedule to design, develop, and validate real-time clinical software systems. This role blends technical leadership with hands-on engineering to ensure reliable, regulatory-compliant software across complex healthcare workflows. The position carries a annual salary of USD 178,131.

Responsibilities

Design, develop, enhance, and maintain complex software components and subsystems that support clinical and healthcare software products, with expertise across C, C++, VC++/MFC/COM/ATL, C#.NET, Java, and Objective-C.
Engage in full software development lifecycle activities, including requirements analysis, system and software design, implementation, build and deployment, verification and validation, release planning, risk analysis, and configuration management.
Define and contribute to the architecture of real-time and distributed clinical software systems to ensure reliability, performance, and scalability.
Implement and support healthcare system interoperability and secure data exchange between clinical systems in alignment with industry standards and regulatory requirements.
Develop, integrate, and validate secure communication mechanisms to protect clinical data exchanged across distributed healthcare and medical device environments, including TLS for unicast and custom secure protocols for multicast.
Design, optimize, and automate clinical workflows across imaging, patient monitoring, and hospital systems to improve operational efficiency and clinical usability.
Coordinate and lead software engineering activities by providing technical guidance, conducting design and code reviews, and mentoring engineers to ensure timely, high-quality delivery.
Contribute to the development and validation of clinical software features while ensuring compliance with internal SOPs and FDA regulations and medical device software standards.
Support audit trails, requirements traceability, post-market surveillance, and adherence to regulatory requirements.
Drive modernization of existing software systems by improving architecture, maintainability, and scalability while preserving validated clinical workflows, including refactoring and migrating monolithic C++/C# codebases without disruption.
Plan and execute software verification activities, including unit, subsystem, and integration testing, as well as defect reproduction, analysis, and resolution.

Requirements

Bachelor’s degree in Electronics Engineering, Computer and Information Technology or related field, plus five years of progressive post-degree experience.
Experience performing software development in C, C++, VC++/MFC/COM/ATL, C#.NET, Java, and Objective-C.
Experience with the full SDLC including requirements analysis, architecture, design, implementation, verification/validation, release planning, risk analysis, and configuration management.
Experience in the design and architecture of real-time clinical systems, including deterministic systems, server applications, and distributed communication frameworks.
Proficiency implementing healthcare system interoperability and secure data exchange using standards such as DICOM, HL7, IHE, and HIPAA-compliant protocols.
Experience developing and integrating secure communication frameworks, including TLS for unicast and custom protocols for multicast.
Ability to design and automate clinical workflows across imaging systems and the broader hospital device ecosystem.
Experience leading and mentoring engineering teams, providing architectural guidance, conducting code reviews, and coordinating cross-team efforts.
Experience implementing image processing algorithms for ACR accreditation tests and ensuring FDA software and regulatory compliance related to 21 CFR Part 11, IEC 62304, and ISO 13485.
Experience performing audit trails, traceability, post-market surveillance, and SOP compliance.
Experience driving legacy system modernization, including refactoring and migrating monolithic C++/C# codebases without disrupting validated workflows.
Proven ability to execute engineering and reliability verification through unit, subsystem, integration, stress/scale testing and detailed defect analysis.

Technologies

C
C++
VC++/MFC/COM/ATL
C#.NET
Java
Objective-C

Benefits

Medical, dental, and vision insurance
Life, short- and long-term disability coverage
401(k) with company match
Over 4 weeks of paid time off, plus holidays and parental leave
Flexible spending accounts and employee assistance program
Free parking, on-site gym, cafeteria, and game room (select locations)

About Draeger

Draeger emphasizes the guiding principle “Technology for Life” and offers opportunities across North America. The North America headquarters is in Telford, PA, just north of Philadelphia, with US sites in Andover, MA and Houston, TX, and a Canada site in Mississauga, Ontario. Draeger is an Equal Opportunity Employer.

How to apply

Please apply directly through our career portal. We look forward to receiving your application.

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1mo ago

Sr Software Engineer - Windows Applications

Draeger Medical Systems, Inc. Andover, MA

Andover, MA

1mo ago Closed

$115k - $127k/yr Full time Senior Developer Engineering

This position is no longer accepting applications (closed Jul 10, 2026).

Job Description

Responsibilities

Collaborate with cross-functional teams of engineers and test professionals to deliver high-quality software across all phases of development, including design, implementation, integration, testing, and support
Design and develop software architectures, translate technical specifications into robust solutions, and deliver well-tested, maintainable code
Diagnose, troubleshoot, and resolve complex software defects independently
Provide technical leadership, including defining requirements, guiding design decisions, and mentoring team members
Coordinate engineering activities and drive timely delivery of software modules and subsystems by establishing clear goals and expectations
Perform and guide unit, subsystem, and integration testing to ensure software quality and reliability, while promoting best testing practices across the team
Support system-level activities by partnering with clinical, quality, service, and test engineers to reproduce issues, execute tests, and document findings in defect tracking systems
Contribute to program planning, strategic initiatives, and continuous process improvements across the organization
Mentor and support the development of junior engineers through technical coaching, code reviews, and feedback
Ensure compliance with internal standard operating procedures and applicable FDA and industry regulations
Maintain and improve software development processes, tools, and configuration management practices

Requirements

5 to 8 years of experience in software design, analysis, and troubleshooting in an engineering environment, or 3 to 6 years with a Master's degree
Proven experience providing technical leadership within a complex software development environment
Strong background in Windows application development, including Win32 and MFC
Experience with Windows batch scripting
Demonstrated curiosity and ability to explore Windows internals to diagnose and resolve complex system behaviors
Proficiency in C++ and Python
Experience debugging applications using Visual Studio
Working knowledge of TCP/IP and UDP networking
Ability to elicit, document, analyze, review, and trace software requirements
Bachelor's degree

Technologies

Win32
MFC
Windows batch scripting
C++
Python
Visual Studio
TCP/IP
UDP networking
C#
CMake
Ninja
UWF
Secure Boot
BitLocker

Benefits

Medical, dental, and vision insurance
Life, short- and long-term disability coverage
401(k) with company match
Over 4 weeks of paid time off, plus holidays and parental leave
Flexible spending accounts and employee assistance program
Free parking
On-site gym
Cafeteria
Game room

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1mo ago

Software Engineer II

Draeger Medical Systems, Inc. Andover, MA

Andover, MA

1mo ago Closed

$91k - $101k/yr Full time C++ Database Developer

This position is no longer accepting applications (closed Jul 6, 2026).

Job Description

Draeger Medical Systems, Inc. offers a hybrid Software Engineer II role based in Andover, MA within R&D. You will contribute to software architecture, design, implementation, testing, and ongoing improvements to development efficiency, software quality, and product cost. The position carries a salary range of USD 91,299 - 100,900 per year.

This role supports collaboration across clinical, quality, service, and test personnel to deliver robust software solutions in a dynamic, regulated environment.

Responsibilities

Collaborate with a team of engineers and test personnel to produce high quality deliverables across design, implementation, integration, testing, and support phases of product development.
Diagnose, debug, and resolve defects with minimal supervision.
Design small software modules and functions.
Translate designs into functional, tested software.
Adhere to internal SOPs as well as FDA and industry regulations.
Utilize the software configuration management system to maintain software files correctly.
Build software and install it in development and product environments.
Support clinical, quality, service, and test personnel by executing tests, reproducing defects, and documenting defect analysis in a defect tracking tool.
Take direction from senior engineering staff and seek guidance as needed; respond to coaching.
Analyze successes and failures to drive improvements and tackle unfamiliar tasks.
Provide feedback during code and design reviews.

Requirements

2-5 years of hands-on experience in software design, analysis and troubleshooting in an engineering environment (1-3 years of experience with a MS degree).
Ability to effectively provide code and design feedback and communicate internally.
C/C++ development experience.
Experience with one of the following: Red Hat Enterprise Linux, UNIX/Linux development environment tools, or UNIX/Linux systems programming.
Qt software development framework experience or equivalent GUI experience.
NoSQL database development technologies.
TCP/IP programming experience.
Bash shell scripting.
Wireshark packet capture analysis experience.
X11 Windows programming.
Education: BS in Computer Science or Electrical Engineering.

Technologies

C/C++ Development
Qt Software Development Framework
NoSQL Database Development Technologies
TCP/IP Programming
Bash Shell Scripting
Wireshark Packet Capture Analysis
X11 Windows Programming
Red Hat Enterprise Linux
UNIX/Linux Development Environment Tools
UNIX/Linux Systems Programming

Benefits

Medical, dental, and vision insurance
Life, short- and long-term disability coverage
401(k) with company match
Over 4 weeks of paid time off, plus holidays and parental leave
Flexible spending accounts and an employee assistance program
Free parking, an on-site gym, cafeteria, and game room

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2mo ago

Associate Engineer, RNA Starting Material MS&T

Sarepta Therapeutics Andover, MA

Andover, MA

2mo ago Closed

$62k - $78k/yr Full time Biotech Pharma Engineering Manufacturing

This position is no longer accepting applications (closed Jun 16, 2026).

Job Description

The Associate Engineer, RNA Starting Material MS&T role at Sarepta Therapeutics in Andover, MA focuses on supporting synthesis, purification, analysis, and characterization of nucleoside-based and lipid building blocks for PMOs, next-generation PMO, and siRNA platforms, with involvement in development, scale-up, and tech transfer of RNA starting materials manufacturing.

Responsibilities

Collaborate in a team performing lab-scale organic synthesis, purification, analysis, and characterization of nucleoside-based and lipid building blocks used in Sarepta's PMO, next-gen PMO, and siRNA platforms.
Prepare reference markers and standards and contribute to supervised RNA starting materials manufacturing process chemistry development and scale-up projects to optimize routes and troubleshoot syntheses.
Engage in cross-functional training, coordinate with Analytical/QC resources, and interpret data from HPLC, GC, KF, and NMR analyses.
Draft experimental protocols and generate technical reports, applying strong organic chemistry knowledge and problem-solving skills.

Requirements

Bachelor of Science in Chemical Engineering, Chemistry, or a related discipline, with 0-2 years of relevant experience.
Solid grounding in organic chemistry and the ability to interpret data from GC, LC-MS, HPLC, NMR, and KF; practical experience running HPLC methods is strongly preferred.
Ability to manage multiple tasks and meet deadlines in a fast-paced environment.
Effective written and verbal communication skills.
Strong interpersonal skills and meticulous attention to detail.
May require up to 5% travel, domestically or internationally.

Technologies

HPLC
GC
LC-MS
NMR
KF

Benefits

Physical and Emotional Wellness
Financial Wellness
Support for Caregivers

The Importance of the Role

Supports lab-scale synthesis, purification, analysis, and characterization of nucleoside-based and lipid building blocks for PMOs, next-generation PMO, and siRNA platforms.
Contributes to the synthesis of reference markers and participates in supervised RNA starting materials process chemistry development and scale-up to optimize syntheses.
Involves cross-functional training and regular collaboration with Analytical/QC teams, including interpretation of HPLC, GC, KF, and NMR data.
Includes protocol writing and report generation, requiring strong organic chemistry and problem-solving capabilities.

The Opportunity to Make a Difference

Support commercial supply assurance for RNA starting materials by synthesizing nucleoside reference markers and standards.
Execute development studies independently or as part of a supervised team.
Assess scalability of proposed changes and run experiments to mimic large-scale operations.
Participate in technology transfer of improved processes to manufacturing sites.
Build a solid understanding of Sarepta’s manufacturing processes to support process improvements, troubleshooting, and technology transfers.
Perform synthesis and purification of nucleoside analogs to support production and development goals.
Contribute to impurity profiling and collaborative efforts to characterize and manage impurities in intermediates.
Use scientific judgment to identify likely sources of impurities and design experiments to test hypotheses within cross-functional teams.
Compile data, interpret results, document study outcomes, and present conclusions.
Attend vendor update meetings and provide input on ongoing vendor production projects.

More About You

Bachelor of Science in Chemical Engineering, Chemistry, or related discipline, 0-2 years of experience.
Technical competence in organic chemistry and familiarity with GC, LC-MS, HPLC, NMR, and KF data; experience running HPLC methods preferred.
Able to multitask and meet deadlines in a dynamic setting.
Strong written and verbal communication skills.
Excellent interpersonal skills and careful attention to detail.
May require travel up to 5 percent of time, domestically or internationally.

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Engineer Jobs in Andover, MA

Staff Software Engineer

Sr Software Engineer - Windows Applications

Software Engineer II

Associate Engineer, RNA Starting Material MS&T

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