Bausch Health

  • Engineer II - Medical Device

    Location US-NY-Rochester
    Job ID
    Pos. Type
    Full Time
  • Overview

    • This engineer will support new contact lens product & process development activities
    • This engineer will participate and guide process development activities through writing experimental protocols, data gathering, and statistical analysis.
    • The candidate will be proficient in reporting and presentation of data analysis.
    • Candidate will analyze data and provide recommendations on trends, correlations, response variables, DOE’s etc in an effort to better understand process interdependencies.
    • The candidate will work with and help define automation requirements. They will also participate in and guide process capability finalization and process transfer to manufacturing.
    • The candidate will be interfacing with an internal cross functional team while working on these programs.


    • Drive new product & process validations.
    • Design, execute, and analyze experiments.
    • Provide process optimization.
    • Develop and support new manufacturing processes and technologies.
    • Support existing manufacturing processes, quality improvements and cost reductions.
    • Ensure product quality and all tasks are in accordance with established SOPs, GMPs, Divisional Specifications, and EHS standards.
    • Train manufacturing and junior personnel in required operations.
    • May be engineering lead on projects.

    Scope of Position:

    Support and/or Leading product development & process development activities, writing protocols, data gathering and analysis.


    Education:  Degree in Scientific or Engineering Discipline.

    Specialized Training:  Six Sigma Green Belt and DFSS experience preferred.  MiniTab/JMP Statistical software preferred.  Tableau a plus.


    Experience:  Minimum of 3 years in Engineering, Process Development, and/or Quality Engineering setting.  Hands-on experience and technical expertise in a development environment required.  ISO-9000, GMP, medical device manufacturing experience a plus.  Statistical analysis required within a development or manufacturing setting.  Experience with high volume and/or high precision manufacturing a plus.

    Special Skills:  Computer Literacy with skills in Microsoft Excel, Word, and Powerpoint, plus MiniTab, JMP (or equivalent software).  Experience & expertise in Statistical Analysis including DOE and SPC.  Communication, Organization, Report Writing, and Presentation skills a must.  Must be able to develop working relationships with various internal core competencies and work as a team member.


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