Principal Engineer

Bausch Health
Posted on

Type

Practitioner / consultant

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  • Location US-NY-Rochester

Overview

Candidate will be a lead contributor on new contact lens product & process development activities.  This person will perform data analysis and provide statistical based guidance for contact lens R+D product and process feasibility, technology development and technical transfer.  Will ensure robust design of products and processes with understanding of process interdependencies are delivered to global manufacturing facilities while fulfilling our customers’ and commercial needs.  The candidate will be skilled in reporting and presentation of data and subsequent technical recommendations.

Responsibilities

Execute DOEs and provide consultation to others for design of experiments, data analysis, and data modeling and optimization.

Analyze data and provide technical recommendations including process capability and performance analysis

Provide statistical rationale to support sample size justification for sampling plans, validations, etc

Provide leadership for SPC implementation

Provide leadership for process and parameter tolerance setting/budgeting

Standardize and streamline the process of data analysis and report writing for department

Provide training seminars in areas of statistics, quality tools, and data analysis

 

Qualifications

Degree in Scientific or Engineering Discipline.

Special Skills:  Computer Literacy with skills in Microsoft Excel, Word, Project and Powerpoint. Strong Communication, Organization, Report Writing, and Presentation skills a must.  Must be able to develop working relationships with various internal core competencies, manage outside suppliers, influence others outside of their immediate control and lead team members.

Specialized Training:  Six Sigma Black Belt and DFSS experience preferred.  MiniTab/JMP Statistical software preferred, Tableau is a plus. Knowledge of SPC.

10-20 years in Engineering, Process Development, and/or Quality Engineering setting.  Hands-on experience and technical expertise in a development environment a must.  ISO, FDA, medical device manufacturing experience from ideation through commercialization a plus.  Demonstrated use of statistical tools required within a development or manufacturing setting.  Experienced with high volume and/or high precision manufacturing a plus.

Options

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More Information

Posted on

Type

Practitioner / consultant

Irvine%2C%20United%20States

Irvine , United States