Chemical Process Engineer

Trividia Health, Inc.•Lancaster, NH

7h•Onsite

About The Position

Responsible for developing manufacturing processes that minimize waste, maximize efficiency and increase the quality of finished products. Work closely with the engineering, quality, and production teams to improve existing processes and evaluate potential improvements. Work directly with vendors and customers to develop new formulas, or formula iterations. Manage associated documentation to support Process Engineering and R+D functions.

Requirements

Excellent verbal and written communication skills
Ability to present information to both internal and external customers
Ability to read, analyze, and interpret the most complex documents
Ability to respond effectively to the most sensitive inquiries or complaints
Ability to write speeches and articles using original or innovative techniques or style
Ability to make effective and persuasive speeches and presentations on controversial or complex topics to top management, public groups, and/or boards of directors
Ability to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations, and permutations
Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis
Ability to apply principles of logical or scientific thinking to a wide range of intellectual and practical problems
Ability to deal with nonverbal symbolism (formulas, scientific equations, graphs, musical notes, etc.) in its most difficult phases
Ability to deal with a variety of abstract and concrete variables

Nice To Haves

Knowledge of and experience with cGMP manufacturing facility
Association with appropriate engineering, science and industry trade groups
Experience in the pharmaceutical industry

Responsibilities

Monitoring and testing processes and products found in all phases of production
Developing and implementing safety procedures for staff working with dangerous chemicals and hazardous materials
Designing, planning and implementing the layout of manufacturing equipment to optimize production and decrease costs
Creating and executing cleaning protocols and cleaning validations
Staying up to date with new and emerging manufacturing processes
Creating and executing process validations & equipment qualifications
Troubleshooting problems associated with manufacturing processes
Creating and presenting cost analysis reports to upper management
Creating and executing bulk hold studies on finished and WIP goods
Work directly with the process engineering department & QA/QC department to implement process improvements
Work directly with the QA/QC department to facilitate required documentation
Creating and modifying manufacturing records
Creating new and modifying existing formulas