Dräger

Staff Software Engineer

Dräger  •  $178k/yr  •  Andover, MA (Hybrid)  •  2 hours ago
Apply
AI can make mistakes so check important info. Chat history is never stored.

Job Description

Staff Software Engineer

  • Business Unit: Draeger Medical Systems, Inc., Job-ID: 1277
  • Location: Andover
  • Function: R&D
  • Work Location: Hybrid
  • Employment Type: Permanent

The Job Responsibilities

Draeger Medical Systems, Inc., Andover, MA seeks Staff Software Engineers - Design, develop, enhance, and maintain complex software components and subsystems supporting clinical and healthcare software products that include performing software development in C, C++, VC++/MFC/COM/ATL, C#.NET, Java and Objective-C. Perform 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 and design of real-time and distributed clinical software systems, ensuring reliability, performance, and scalability. Implement and support healthcare system interoperability and secure data exchange between clinical systems in compliance 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 integrated 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 and high-quality delivery of software modules and subsystems. Contribute to the development and validation of clinical software features while ensuring compliance with all internal SOPs and FDA regulations and medical device software standards. Ensure adherence to internal standard operating procedures and regulatory requirements by supporting audit trails, requirements traceability, and post-market surveillance activities. Drive the enhancement and 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 disrupting validated workflows. Plan and execute software verification activities, including unit, subsystem, and integration testing, as well as defect reproduction, analysis, and resolution.

Your Qualifications

Requires Bachelor’s (or foreign educ. equiv.) Degree in Electronics Engineering, Computer and Information Technology or related field and five (5) yrs. (post-degree, progressive) experience in Job Offered or related. Experience must have included Performing software development in C, C++, VC++/MFC/COM/ATL, C#.NET, Java and Objective-C; Full software development lifecycle including requirements analysis, architecture, design, implementation, verification/validation, release planning, risk analysis, and configuration management; Design and architecture of real time clinical systems including deterministic systems, server applications and distributed communication frameworks; Implementing and ensuring healthcare system interoperability and secure data exchange using standards including DICOM, HL7, IHE, and HIPAA-compliant protocols; Developing and integrating secure communication frameworks, including TLS for unicast and custom secure protocols for multicast; Designing and automating clinical workflows across imaging systems and the broader hospital device ecosystem; Leading and mentoring engineering teams, including architectural guidance, code reviews and cross-team coordination; Implementation of image processing algorithms for the ACR accreditation tests to determine the quality of the MRI coil elements and ensuring FDA software and regulatory compliance as it relates to 21 CFR Part 11, IEC 62304 and ISO 13485; Performing audit-trail, traceability, post-market surveillance and SOP compliance; Driving legacy system modernization, including refactoring and migrating monolithic C++/C# codebases without disrupting validated workflows; and Executing engineering and reliability verification through unit, subsystem, integration, stress/scale testing and detailed defect analysis. $178,131/yr.

Send resume to amy.covely@draeger.com and must refer to Ref. #1277.

Dräger Benefits

At Draeger, Technology for Life means supporting our people in every aspect of their lives. We offer a competitive benefits package that may include:
  • 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
Select locations also offer free parking, an on-site gym, cafeteria, and game room.
Talk to your Draeger recruiter to learn more!

Who we are

We’re hiring! If you want your contributions to make a real difference, check out this new career opportunity with us at Draeger where we are led by the guiding principle “Technology for Life”.
Draeger has several sites located across North America as well as field-based sales and service positions. Our North America headquarters is located in Telford, PA just north of Philadelphia. We also have US sites in Andover, MA, and Houston, TX. Our Canada site is located in Mississauga, Ontario.
Draeger is an Equal Opportunity Employer.

Interested?

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

Dräger

About Dräger

Dräger is an international leader in the fields of medical and safety technology. The family-owned company was founded in Lübeck, Germany, in 1889. The company’s long-term success is based on the four key strengths of its value-driven culture: customer intimacy, professional employees, continuous innovation and a commitment to outstanding quality.

Dräger offers its customers anaesthesia workstations, medical ventilation, patient monitoring as well as neonatal care for premature babies and newborns. With ceiling supply units, IT solutions for the OR, and gas management systems the company is at the customer’s side throughout the entire hospital.

Emergency response services, law and regulatory enforcement and the industry trust in Dräger’s integrated hazard management, in particular for personal protection and plant safety. This includes: respiratory protection equipment, stationary and portable gas detection systems, professional diving equipment and systems, as well as alcohol and drug impairment detection. In collaboration with its customers Dräger develops customized solutions, such as entire fire training systems, training concepts and workshops.

Dräger has more than 13.700 employees worldwide and is currently present in more than 190 countries. The company has sales and service subsidiaries in over 40 countries. Its development and production facilities are based in Germany, Great Britain, Sweden, South Africa, the USA, Brazil, the Czech Republic and China.

http://t4.life/dataprotection

Drägerwerk AG & Co. KGaA

Board of Managing Directors:

Stefan Dräger (Chairman),

Rainer Klug,

Gert-Hartwig Lescow,

Dr. Reiner Piske,

Anton Schrofner

Company registered at Lübeck Local Court

Register of Companies Number: HRB 7903 HL

Turnover tax identification number as per § 27a

Turnover Tax Law: DE 135082211

General partner:

Drägerwerk Verwaltungs AG

Company registered at Lübeck Local Court

Register of Companies Number: HRB 7395 HL

Industry
Manufacturing & Production
Company Size
10,000+ employees
Headquarters
Lübeck, DE
Year Founded
1889
Social Media