Automation Engineer II

NorthStar Medical Radioisotopes•Beloit, WI

2d•Onsite

About The Position

The Automation Engineer II will contribute to the development and execution of automation engineering tasks through design, planning, procurement, and execution, as well as coordinating with vendors and contractors. Some of these tasks include programming of PLC and HMI as well as associated documentation. Also included are assisting in the development and implementation of Manufacturing Execution Systems (MES) and associated networking and data management systems. This individual will be required to work with cross functional teams, including RA/QA and Process Engineering to apply efficient cGMP processes to preserve data integrity and the quality of the drug product, including the safety of all production and non-production personnel. The Automation Engineer II is responsible performing automation engineering tasks for the support of automated production systems at the Beloit campus. This includes the support of existing production system automation control software and hardware and transfer of automated equipment/systems and the associated control systems into production and providing the ongoing support of these systems to include some standby support. The Automation Engineer II will have responsibility on a project level from conception to final commissioning and validation. This position supports production in a 24-hour manufacturing facility and may require availability to provide support during evenings, nights, weekends, and some holidays, as needed (generally up to 15%).

Requirements

Bachelor’s degree in Engineering and minimum three (3) years of experience with a concentration in Automation or Process Control; or combination of education and experience.
Knowledge of automation hardware design and maintenance required.
Specific knowledge of Siemens automation products and experience in a regulated pharmaceutical/medical device manufacturing environment is preferred.
Each successful applicant will be required to complete the Form I-9, Employment Eligibility Verification, demonstrating both identity and employment authorization, on or before the first day of employment.
Under federal law, only truthful information may be provided on the Form I-9.

Nice To Haves

Specific knowledge of Siemens automation products and experience in a regulated pharmaceutical/medical device manufacturing environment is preferred.

Responsibilities

Design, revise and commission PLC, HMI, and DCS based automation systems with input from cross-functional teams and senior staff.
Design, code, test, debug and document programs and systems as needed in support of new designs and current production systems.
Implement automation changes to existing control system hardware and software, supervising hardware and software modifications done by outside vendors, and development of specifications and testing documentation.
Create, modify, and maintain automation system documentation including project documentation, specification documents, and SOPs in a cGMP compliant state.
Troubleshoot various automation systems and provide training to operations personnel on automated operations.
Ensure effective maintenance and availability of automation system controls and equipment.
Provide automation technical knowledge for troubleshooting, investigations and training associated with Automation software as well as integrated automation system related hardware including sensors, valves, pneumatics, conveyors, robotics, vision systems, filling systems, automatic packaging equipment, etc.
Support the validation of automation systems per cGMP and Regulatory guidance.
Provide automation system design in relation to data acquisition, integrity and retention, required for system tracking and trending, including development of data interfaces between disparate systems to include 21CFR Part 11 and Annex 11.
Understand and create electrical schematics and wiring diagrams and present drawings and project progress to peers and management.
Participate in process risk and hazard reviews and modify equipment/designs as necessary to ensure safe operation and appropriate specifications are captured.
Understand and interpret P&ID drawings, electrical schematics and wiring diagrams; PLC based logic and system integration (Siemens TIA preferred); and NFPA, UL, CE, NEC requirements.
Continuously adapt to an ever-changing regulatory environment such that the Company is in compliance with current regulations.
Develop and strengthen team capabilities through mentoring, training, and technical oversight of less experienced engineers.