Hologic

Systems Engineer, R&D Cytology

Hologic$97K — $152K *
Healthcare
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • BSc/BA in Engineering with 5-8 years or MSc/MA with 3-5 years experience in relevant industries.
  • Certified Systems Engineering Professional (INCOSE ASEP, CSEP) preferred.
  • Experience in electromechanical design, automation, robotics, and embedded firmware development, preferably in medical devices.
  • Strong systems integration skills across mechanical, electrical, and software components.
  • Proficient in SolidWorks and equivalent CAD tools.
  • Knowledgeable in Design for Manufacturability (DFM), Design for Test (DFT), and FMEA methodologies.
  • Good communication skills with the ability to collaborate across departments.

Responsibilities

  • Select new concepts and approaches for electromechanical design and development.
  • Conduct engineering analysis and cost evaluations of designs and processes.
  • Perform formal requirements engineering following INCOSE standards.
  • Document mechanical specifications, designs, and technical procedures.
  • Implement new electromechanical designs within scheduled cost and performance criteria.
  • Provide technical consultation for ongoing product improvement and problem investigations.
  • Collaborate with cross-functional teams such as Manufacturing, Service, and Supply Chain.

Benefits

  • Hybrid work environment.
  • Opportunity to contribute to innovative product development in the medical field.
  • Engagement with cross-functional teams, enhancing collaborative skills.
  • Potential for personal and professional growth in a leading company.
Full Job Description
Job Description

In this role, you will be responsible for a wide range of product development activities including the specification, design, component selection, systems integration, verification testing of electromechanical subsystems.

This is a hybrid position in Marlborough, MA.

Essential Duties and Responsibilities
  • Selection of new concepts and approaches for the electromechanical design/development of new or improved products and processes
  • Performs engineering analysis, performance and cost evaluations of the aforementioned designs and processes.
  • Formal requirements engineering per INCOSE standards.
  • Communicate effectively & constructively with peers, suppliers, and external design partners.
  • Responsible for engineering documentation of mechanical specifications, designs, modifications, and technical procedures
  • Responsible for the implementation of new electromechanical designs, modifications, etc. within a scheduled cost and performance criteria
  • Provide technical consultation for existing product line problem investigation and ongoing product improvement.
  • Experience in the design of new products involving mechanisms, automation, firmware, optics, and electromechanical systems.
  • Ideate, design and prototype fixtures and establish methods to support design verification/validation activities.
  • Work with cross-functional teams that include: Manufacturing, Service and Supply Chain.

Expected Education and Experience:
  • BSc/BA Engineering Degree, with 5 - 8 years of experience in relevant industries, or
  • MSc/MA with 3 - 5 years of experience in relevant industries

Required Skills and Qualifications
  • Preferably a Certified Systems Engineering Professional (INCOSE ASEP, CSEP)
  • Experience in a variety of electromechanical design areas including automation, electro-mechanical/robotics, embedded firmware development, particularly in the medical device field.
  • Systems integration experience with marrying electrical, mechanical, and software components.
  • Preferably with knowledge of model-based engineering and SysML.
  • Proficiency using SolidWorks and SolidWorks PDM or equivalent CAD design tools.
  • Understanding of Design for Manufacturability (DFM), Design for Test (DFT), Root Cause, Root Cause Failure Analysis Methodologies, Failure Mode and Effect Analysis (FMEA).
  • Ability to communicate effectively and constructively with peers, and other departments.
  • Programing experience or ability to write embedded code to test designs is a plus.
  • Experience with FDA regulated medical devices is a plus.
  • Experience with servicing medical devices is a plus.
  • Agile PLM or equivalent PLM system knowledge is a plus.

The annualized base salary range for this role is $97,600 to $152,700 and is bonus eligible. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, geography, education, business needs, and market demand.

If you have the right skills and experience, apply today!

#LI-RF1 #Mid-level

Agency and Third Party Recruiter Notice:

Agencies that submit a resume to Hologic must have a current executed Hologic Agency Agreement executed by a member of the Human Resource Department. In addition, Agencies may only submit candidates to positions for which they have been invited to do so by a Hologic Recruiter. All resumes must be sent to the Hologic Recruiter under these terms or they will not be considered.

About Hologic

Hologic, Inc. is an American medical technology company that develops and manufactures diagnostic products, medical imaging systems, and surgical products. The company's products are used in a wide range of medical applications, including breast cancer screening, cervical cancer screening, and osteoporosis diagnosis. Hologic is headquartered in Marlborough, Massachusetts, and has operations in North America, Europe, and Asia. The company was founded in 1985 and has grown to become one of the largest medical technology companies in the world.
Learn more about Hologic
Size
6,705 employees
Market Cap
$18.5 billion
Industry
Net Income
$1.3 billion
Founded
1985
5 Year Trend
+9.7%
Revenue
$4.5 billion
NASDAQ

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