Sorry, this job is no longer accepting applications. See below for more jobs that match what you’re looking for!

Software Development Manager - 149

Expired Job

Infor Saint Paul , MN 55102

Posted 3 months ago

Software Development Manager

St. Paul, MN


  • Manage the day to day activies of direct reports

  • Encourages the growth of all direct and indirect reports

  • Mentor and measure staff performance

  • Maintain technical knowledge

  • Provide reporting and metrics on key initiatives

  • Manage customer issues to resolution

  • Assign and review project work of direct reports setting priorities

  • Resolve problems including identifying causes to prevent reoccurrence


  • Four year Bachelor's degree or Master's degree in Computer Science/Engineering/Mathematics

  • Prior programming experience

  • 5+ years building and managing development teams.


  • Strong communication and organizational skills

  • Ability to manage multiple products and projects

  • Highly motivated with the ability to drive initiatives across multiple development teams

  • Organizational, technical leadership, and interpersonal skills.


  • Prior experience with Infor Products

  • Project management experience

Infor does not discriminate in employment opportunities or practices on the basis of race, color, creed, religion, sex, gender identity or expression, sexual orientation, national origin, genetics, disability, marital status, age, veteran status, protected veterans, military service obligation, citizenship status, individuals with disabilities, or any other characteristic protected by law applicable to the state in which you work.

In compliance with the ADA/AODA, should you have a disability and would like to request an accommodation in order to apply for a currently open position with Infor, please call (678) 319-8000 or email us at

Applicants to and employees of most United States private employers, state and local governments, educational institutions, employment agencies and labor organizations are protected under Federal law from discrimination. For additional information please see EEO is the Law poster, the EEO Supplemental as well as the Statement of Policy.

See if you are a match!

See how well your resume matches up to this job - upload your resume now.

Find your dream job anywhere
with the LiveCareer app.
Download the
LiveCareer app and find
your dream job anywhere

Boost your job search productivity with our
free Chrome Extension!

lc_apply_tool GET EXTENSION

Similar Jobs

Want to see jobs matched to your resume? Upload One Now! Remove
Staff Software Development Quality Engineer

Abbott Laboratories

Posted 1 week ago

VIEW JOBS 12/2/2018 12:00:00 AM 2019-03-02T00:00 At Abbott, we're committed to helping people live their best possible life through the power of health. For more than 125 years, we've brought new products and technologies to the world -- in nutrition, diagnostics, medical devices and branded generic pharmaceuticals -- that create more possibilities for more people at all stages of life. Today, 99,000 of us are working to help people live not just longer, but better, in the more than 150 countries we serve. JOB DESCRIPTION: We are seeking an experienced, high caliber Staff Software Development Quality Engineer. This position is responsible for maintaining a strong collaborative partnership with cross-functional team members that facilitates organizational success by protecting patient/user safety and meeting business needs. We are team-oriented, fast-paced and progressive. We value people with great ideas who partner with others both internally and externally to take action and accomplish goals. Impact this role will have on Abbott: * Oversee and manage the operational aspects of ongoing SW projects activities * Compliance with SW development and validation SOP/WIs and participate in process improvement initiatives * Develop mechanisms for monitoring project progress and for intervention and problem solving with software teams * Design verification and validation test planning and execution * Design verification and validation test protocols and reports * Design input output trace matrix * Quality Planning, including internal product development, OEM-based, Clinical Product Development (CPDP), and design change projects * Provides project management assurance that software products meet customer requirements. Monitors and analyzes quality trends in software to assure that quality problems are resolved, achieving cost and quality improvements and customer satisfaction. * Fosters communication and cooperation between software quality, software development, information technology, software support teams and the user community. * Promote risk based validation process by ensuring the defined software validation policies and procedures are appropriate and followed for each system being validated. * Ensure DHF content completion, integrity, and regulatory & standards compliance; collaboratively communicating & resolving gaps * Requirements review * Lead Risk Management activities from product Concept through Commercialization * Design specification reviews * Design change plan/reports * Ability to work independently with minimal/no supervision * Ability to coach/mentor junior and/or entry-level Engineering personnel/staff * Maintain high standards for content completion, integrity, and regulatory & standards compliance; collaboratively identifying, communicating & resolving gaps * Comply with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, company policies, operating procedures, processes, and task assignments * Maintain positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors * Support all Divisional initiatives as identified by divisional management and in support of quality management systems (QMS), environmental management systems (EMS), and other regulatory requirements * Perform other duties and responsibilities as assigned by functional management based on the current project/business objectives including 10% travel, including international travel and regular predictable attendance Your experience(s), education and knowledge will further expand Abbott's marketplace success: * Bachelor level degree in an Engineering Discipline * 10+ years' experience * Previous Quality engineering experience and demonstrated use of Quality tools/methodologies * Working understanding of FDA, GMP, and ISO 13485 * Solid verbal, written, and interpersonal skills with ability to effectively communicate at multiple levels in the organization * Ability to leverage and/or engage others to accomplish projects. * Multitasks, prioritizes and meets deadlines in timely manner. * Ability to work both within a team, and independently, in a fast-paced, changing environment. * Project management experience Your preferred qualifications and education: * Advance degree * Prior medical device experience preferred * Degree in Mechanical, Biomedical, or Electrical Engineering * Team leadership experience * R&D Experience * Experience working in a broader enterprise/cross-division business unit model * Working understanding of the following standards 60601, 14971, &/or 62304 JOB FAMILY:Engineering DIVISION:CAHF Cardiac Arrhythmias & Heart Failure LOCATION:United States > Minnesota : One St Jude Medical Drive ADDITIONAL LOCATIONS: WORK SHIFT:Standard TRAVEL:Yes, 10 % of the Time MEDICAL SURVEILLANCE:Not Applicable SIGNIFICANT WORK ACTIVITIES:Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday) Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans. EEO is the Law link - English: EEO is the Law link - Espanol: Abbott Laboratories Saint Paul MN

Software Development Manager - 149

Expired Job