Senior Process Engineer

Phibro•Salisbury, MD

3d•Onsite

About The Position

Phibro Animal Health Corporation is a publicly traded, global organization with a rich history in animal health and nutrition as a manufacturer and marketer of medicated feed additives, vaccines, nutritional specialty products, and mineral nutrition. We strive to be a trusted partner with livestock producers, farmers, veterinarians, and consumers who raise or care for farm and companion animals by providing solutions to help them maintain and enhance the health of their animals. Phibro is a diversified company in manufacturing and marketing products for ethanol performance, microbials for plants, home and industrial applications, and specialty chemicals for various industrial markets. In addition to, Phibro’s revenues are in excess of $1 billion and are supported by over 2,400 employees worldwide. At Phibro, people are our greatest asset. We strive to develop a diverse workforce that fosters an environment where people feel supported in openly sharing their creativity and skills that allows them to be the most successful that they can be. If you are interested in working for Phibro and feel that you do not meet all qualifications, we encourage you to apply as you might be the right candidate for this role or other positions. The Senior Process Engineer is an integral part of our Environmental Health & Safety team based out of our US - Salisbury, MD Plant site. Compensation range for this position is $100,000.00 - $130,000.00 Position Summary This position will be responsible for providing process engineering support of all Capital Expenditures, Equipment design, Production equipment layouts, Equipment purchases and Installations, Validation/Qualifications for Equipment and Processes, as well as Maintenance and Engineering for the site. The ideal candidate will use industry best practices to measure, analyze and specify requirements that lead to best in class quality products and design for manufacturability. We are looking for a highly motivated candidate, who can work cross-functionally.

Requirements

BS/MS in Engineering (Chemistry, Chemical Engineering, Material Engineering and/or Biology preferred) with 5+ years of experience in a manufacturing environment.
Food and Drug Administration, USDA and/or Drug Product Formulation & Aseptic Manufacturing experience is required.
Experience with Dust Control
Strong ability to do root-cause problem solving, and implementation of effective preventative action.
Able to interact effectively with all levels of colleagues and management across organizational boundaries.
Possess flexibility and agility to respond to constantly changing conditions and priorities.
Proficient computer skills such as Excel, Word, MS Visio, JMP, Minitab, Solid Works, or similar software.
Must be willing to quickly learn and become proficient in common systems used to manage the business – to include production schedule, quality deviations, ERP system, and change control.
Strong attention to detail

Responsibilities

Lead projects relating to the development and optimization of production processes, including plant design, process equipment/workflows, material handling and automation.
Evaluate existing manufacturing processes for improvements in capacity, efficiency and product quality in alignment with business needs.
Support production non-conformances and attend the Quality review meetings for technical expertise and disposition of product.
Investigates root cause of production issues impacting product quality or yield, support implementation of improvement and countermeasures.
Identify sources of variation within the manufacturing process and design solutions.
Develop user requirements for new capital equipment, survey potential equipment suppliers, submit RFQs, evaluate proposals from suppliers and provide recommendations for purchase.
Responsible for the entire capital process and all capital expenditures.
Recognizes need for and embraces concept of continuous improvement.
Creates new ideas and recommendations based on engineering data, facts, and observations.
May lead improvement tasks depending on their scale.
Create project timelines for validations/material qualifications that include risk mitigations to achieve required timelines.
Effectively partners with and motivates enabling support teams to improve operations for the advancement of the whole site and company.
Support quality control and safety standards.
Actively contribute to meeting business objectives around compliance, cost savings, and potentially capital spend requirements.
Identify, develop, plan, and implement Automation Opportunities for the site
Identify, develop, plan, and implement Process Improvement activities across the site.
Learn, and Understand the site Budgetting process for the Salisbury facility
Identify, Write, Execute, and provide Final Summary for all Validation and Qualifications for the Salisbury facility.
Have all Electrical and Mechanical P&ID drawings updated to our current state.
Work closely with the Regulatory & Technical groups to develop Quality centric process Improvements for the site.
Verify control schemes, interlocks, and safety devices designed by contractors
Maintain Distributive Control Systems and Programmable Logic Controllers in a valid state as required by the FDA
Train Production Operators in the proper operation of new equipment
Communicate with individuals at other facilities to coordinate process developments
Monitor, improve, and control Production output for each line to ensure that plant goals are achieved.
Responsible for updating all paperwork for the Production area, from daily output to lot specific batch sheets (when needed) as well as all Quality related items.
Coordinate with Production, Quality, and Maintenance Departments to develop strategies to increase production, such as: improvement of potencies, reduction of costs, and process control.
Other duties may be identified and assigned as necessary