Manufacturing Engineer - Automation Lifecore Biomedical Inc.
THIS JOB HAS EXPIRED Job Description:
In this position, you will gain a detailed knowledge of, and contribute to process, manufacturing, and packaging engineering activities within Lifecore. You will investigate and correct problems involving the manufacturing processes and equipment, which adversely affect the process results; collect and analyze relevant process data to aid in changes which improve the manufacturing process; interact with all appropriate departments to facilitate the introduction of new manufacturing processes or changes to existing manufacturing processes; perform the installation of new manufacturing equipment and systems; ensure compliance with the Quality System and Design Control requirements; assist Maintenance in diagnosing equipment failures; ensure engineering project timelines are met and that each project meets the demands set forth by the Manufacturing Schedule; support the execution of experiments to identify solutions for satisfying manufacturing problems; demonstrate an understanding of the fermentation and syringe manufacturing process; demonstrate the ability to perform tasks associated with standard operating procedures and document understanding of the tasks during training; assist other departments as needed.
BS in Engineering or Automation Engineering Technology Degree with up to 5 years experience in a manufacturing environment; preferably medical device or biopharmaceutical.
?Hands On? mechanical aptitude and Engineering skill. Understanding of (cGMP) including acceptable documentation practices (i.e. SOP?s, preventative maintenance procedures, and technical drawings). Proficient in Microsoft Word, Excel with AutoCAD Electrical experience desirable. Ability to read and understand automation electrical wiring schematics. Planning and prioritizing skills related to long and short range goals.
Ability to work proactively with department supervisors to create a more robust manufacturing operation. Understanding of basic regulatory requirements affecting medical device and drug manufacturing, including software validation, design control, and tech transfer. Ability to implement and assist in the validation of all new automated equipment. Demonstrate understanding (i.e. programming, troubleshooting failures?) of Automation Electronics such as PLC?s and HMI?s (specifically Allen-Bradley), VFD?s, PID Controllers, Servo Drives, Vision Cameras, sensors, etc.
Medical and Dental Coverage
Flexible Spending Accounts
Short and Long Term Disability
Generous Paid Time Off
Employee Assistance Program
Hours: 5 day work week
||Chaska, MN |
THIS JOB HAS EXPIRED