Position: Entry level

Job type: Full-time

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Job content

Summary

PerkinElmer is seeking a highly motivated candidate to join the Hopkinton Applied Genomics R&D team. This role will be responsible for supporting PerkinElmer Automation Liquid Handling and Microfluidics product lines. This position will require the ability to interface to a multi-disciplinary group as well as cross functions for the timely completion of projects. The successful candidate will have strong software design experience, as well as excellent interpersonal and communication skills required to work in an interdisciplinary environment with an internationally distributed team.

Duties And Responsibilities
  • Improve performance and quality of existing software by solving bugs identified by business, field service support/engineers, manufacturing and assay development teams
  • Actively participate in daily stand-ups to prioritize/assign tasks to external contracting software development partner and ensuring implementation of more effective technical solutions to meet business requirements within given deadlines
  • Provide project status during biweekly software team meeting
  • Software lead on new software functionalities for new assay development; create new release documentation.
  • Champion quality throughout the development process — direct risk assessment and mitigation activities
Education And Experience
  • B.S. or M.S. in Computer Science or equivalent
  • At least 2-3 years of industry experience in Software Engineering
  • Track record of products launched successfully while executing end-to-end software development life cycle
Job Requirements
  • Proficiency with C#/C++/C programming language and .NET/Visual Studio development
tools
  • Experienced with Agile Scrum development methodologies
  • Experienced with version control (TFS), bug tracking systems and procedures
  • Experience with communication protocols, such as TCP/IP
  • Microfluidics product development experience preferred
  • Firmware development experience preferred
  • Knowledgeable with SQL Server preferred
  • Familiarity with FDA regulations on development of medical device (21 CFR Part 11) preferred
  • Excellent interpersonal, written and oral communication and collaboration skills
  • Strong sense of ownership and detailed-oriented
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Deadline: 09-06-2024

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