Thursday 20 February 2020

Senior Project Engineer for BAXTER @Cleveland, Mississippi.

Hi,
My name is David. I am a Staffing Coordinator at Veda info, I am reaching out to you on an exciting job opportunity with one such direct client.
Please find the below requirement details. Kindly send me your recent updated resume.
Feel free to reach me at 310-589-4480
 
Senior Project Engineer at Cleveland, Mississippi
12 Months contract

About the Position:
This position is a key role in the Injection Molding and Devices. Primary focus will be on implementing continuous improvement, new business, and capacity expansion projects. Additional focus will also be on manufacturing equipment reliability and process support work within the Injection Molding and Devices Operations. Cross-functional project management will be involved in this role as well.
The contract duration should be for 12 months with the option to extend to 24 months depending in final approved project scope, timeline, and funding.
Specific project work for this contract opportunity will include
Upgrading obsolete hardware on existing automated assembly machines (new pressure decay testers, ultrasonic welders, molded part vibratory feeders).
Design/installation/commissioning of multiple new automated device assembly machines into existing cleanroom space.
Modifying existing cleanroom space to match requirements for the new equipment footprint and desired process flow.
Installation/commissioning of new molds and mold machines into existing cleanroom space for new molded components.
Relocation of some existing mold machines to optimize cleanroom space and make room for new mold machines.
Validation/Qualification activities for new molds, machines, assembly equipment, and cleanroom modifications.
Assist Project Manager with required project planning, project controls, and procurement work

Essential Duties and Responsibilities:
Utilize engineering principles to design/modify precision assembly and/or manufacturing equipment.
Manage multiple projects with minimal supervision.
Prepare estimates for various tasks and projects.
Manage capital projects both directly and through coordinating engineers.
Research the purchase of new equipment or upgrades to existing equipment.
Drive Continuous Improvement Activities.
Interface with plant and corporate groups as well as contractors and vendors.
Must be able to interact with all levels of employees and functions such as quality, validation, manufacturing, purchasing, maintenance, etc.
Manage start-up, debug, and commission of new manufacturing processes.
Equipment life cycle management including: upgrades, replacement, and decommissioning
Product life cycle management including: product design changes, material changes, Supplier Notice of Change (SNC) assessments, specification changes, etc.
Provide technical support/troubleshooting to all plant departments.
Demonstrate proactive communication and problem solving.
Responsible for supporting and achieving Value Improvement Projects (VIP's).
Responsible for adhering to FDA Design Control standards at all times.
Responsible for adhering to and maintaining all department Standard Operating Procedures (SOPs), forms, log books.
Perform process reviews and prepare technical reports detailing equipment operation and preventative maintenance.
Develop User Requirement Specifications, Technical Specifications, and Design Specifications for new equipment or upgrades to existing equipment.
Author and executes protocols to include FAT, SAT, IQ, OQ and PQ.
Must be able to read and interpret blueprints, technical drawings, schematics, and computer-generated reports.
Must be able to meet all cleanroom garbing & personnel protective equipment (PPE) requirements for areas of manufacturing where work needs to be done.
Must be able to work flexible hours including some overtime work on nights and weekends as needed to support manufacturing/project activities.

Qualifications:
Bachelor degree in Engineering required. (Mechanical, Industrial, Electrical, or Computer degrees are preferred)
7+ years Engineering / Manufacturing experience required. FDA manufacturing experience is preferred.
Programming/troubleshooting experience with automation controls, automated assembly, control systems, PLC's, HMI's, servo's, and vision inspection systems is preferred.
Programming/troubleshooting experience with BMS, HVAC, automated assembly is preferred.
Design software experience (like AutoCAD, Solid Works, etc.) is preferred.
Six Sigma Master Black Belt Certification or industry standard equivalent is preferred.
Plastic injection molding experience is a plus.
Project Management skills and experience (including Microsoft Project software) are a plus.
Lean Manufacturing skills and experience are a plus
 
Thanks,
David Miller
Senior Recruiter
Phone: 310-589-4480
Vedainfo Inc, Hawthorne Blvd, Suite B-01, Torrance, CA 90505
Sent by david@us.vedainfo.com in collaboration with
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