Manufacturing/Production Engineer-I position at A10 in Raritan

A10 is currently seeking to employ Manufacturing/Production Engineer-I on Fri, 31 May 2013 01:22:58 GMT. Manufacturing/Production Engineer-I Location : RARITAN, NJ Position Type : Contract Experience Level : Start Date / End Date : 06/03/2013 / 06/02/2015 Description PRODUCTION ENGINEER (1of 2 Description Global Supply Chain, Medical Devices and Diagnostics (MD&D) is recruiting for a Manufacturing Engineer. This position will support Ortho-Clinical Diagnostics (OCD) in Raritan, NJ. Medical...

Manufacturing/Production Engineer-I

Location: Raritan New Jersey

Description: A10 is currently seeking to employ Manufacturing/Production Engineer-I right now, this position will be placed in New Jersey. Further informations about this position opportunity kindly see the descriptions. Location :
RARITAN, NJ

Position Type : Contract

Experience Level :
Start Date / End Date : 06/03/2013 / 06/02/2015
Description
PRODUCTION ENGINEER (1of 2

Description

Global Supply Chain, Medical Devices and Diagnostics (MD&D) is recruiting for a Manufacturing Engineer. This position will support Ortho-Clinical Diagnostics (OCD) in Raritan, NJ. Medical Devices & Diagnostics Global Services, LLC., represents more than 60 manufacturing sites and 26,000

employees who plan, source, manufacture and deliver high-quality and cost-effective medical products to our customers around the globe each day. Work of the MD&D SC supports a multitude of product platforms, new products and delivery systems that are used in a wide range of procedures throughout the healthcare industry, including interventional cardiology, electrophysiology, minimally invasive surgery, hospital sterilization, clinical laboratory testing, diabetes management, joint replacement surgery and vision care. Ortho Clinical Diagnostics serves the transfusion medicine community and laboratories around ! the world. We're a leading provider of total solutions for scr! eening, diagnosing, monitoring and confirming diseases early, before they put lives at risk. Our single focus is to help hospitals, laboratories and blood centers worldwide deliver results that help patients experience a better quality of life. For more information please visit www.orthoclinical.com

The Manufacturing Engineer will be responsible for:
•Managing and closing aged non-conformances/aged corrective action-preventive action (CAPAÂ's)

•Managing and closing aged Change Orders (CO) Assisting in resolving manufacturing & process challenges

•Provide maintenance systems support including equipment reliability, as needed

•Assisting in developing robust processes, simplifying Router Structure/accuracy

•Creating Standard Operating Procedures (SOPÂ's) and training documentation, as required

The Manufacturing Engineer will plan, determine funding, and coordinate manufacturing projects as assigned to meet c! ost, quality, safety and environmental criteria. The individual will work in direct support of the Raritan business operating units and designated project teams to support equipment upgrades and process improvements. Responsibilities will also include developing, coordinating, documenting, and delivering equipment with the associated regulatory and change management actions.

Qualifications

Requires a minimum of a Bachelors degree in an Engineering discipline plus a minimum of 2 years of medical device and/or pharmaceutical facilities and/or manufacturing project management experience. Candidate must possess excellent verbal and written communications skills to convey technical content to management and auditing agencies as required. Must also be knowledgeable of cGMP based process and equipment validation activities. Must have a working knowledge of engineering and project controls required in the successful design and construction of production and facili! ty systems.

System knowledge specifically in the following are! as is desirable: PLC programming, vision systems, labeling equipment, servo motors and automated filling, packaging and assembly equipment. Knowledge of FDA and other regulatory guidance is helpful. Sterile manufacturing, Six Sigma Methodology Certification, Aseptic processing and parenteral knowledge is desirable. Proficiency in Microsoft MS Office Suite (Word, Excel and PowerPoint) is required. This position will be based in Raritan, NJ.
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If you were eligible to this position, please email us your resume, with salary requirements and a resume to A10.

If you interested on this position just click on the Apply button, you will be redirected to the official website

This position starts available on: Fri, 31 May 2013 01:22:58 GMT



Apply Manufacturing/Production Engineer-I Here

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