St Jude Medical Requires TCE Program Analyst for Penang

St Jude Medical Requires TCE Program Analyst for Penang

St Jude Medical Requires TCE Program Analyst for PenangSt. Jude Medical, a Fortune 500 company is a premier high-tech medical device company that develops innovative medical technology, products and services that improve the lives of patients all over the world. A St. Jude Medical device is implanted into a human being every 3 seconds of every hour of every business day. Headquartered in St. Paul, Minnesota, St. Jude Medical is a global company with research, development and manufacturing facilities around the globe. We have four focus areas that include cardiac rhythm management, atrial fibrillation, cardiovascular and neuromodulation. Our products treat patients in more than 100 countries and we employ more than 15,000 people worldwide.

St. Jude Medical in Penang is our latest state of the art facility involved in the manufacturing of life saving devices. We plan to invest US$300 million over the next few years in our Penang facility and create more than 1,000 career opportunities.

If you would like to join us in saving lives, we would like to hear from you! Selected individuals will be trained and certified in an innovative and high technology environment.

Position: TCE Program Analyst
Work Location: Penang

Responsibilities:
  • Administer Team Center Engineering (TcE) system, provide application support, design and develop customization programs.
  • Architecture solution to PDM/PLM interfaces like ERP, MES and other enterprise systems.
  • The candidate should have good knowledge in managing the projects, and should be a good team player work with other co-site administer.

Requirements:
  • Degree in Computer Science or any Engineering
  • At least 5 years experience in managing Siemen’s PDM/PLM systems (Preferably in Team Center Engineering)
  • Provide direct expertise in TcE software installation and configuration
  • Design and develop TcE ITK, Java, C++ programming for customizations
  • Good knowledge in Oracle database, SQL, PL/SQL, Unix Shell scripts and Perl scripting
  • Good knowledge in Linux (Preferable Suse or RedHat)
  • Good knowledge in middleware apps Jboss, WebLogic or WebSphere
  • Good knowledge in ERP system (Preferable in SAP and Mfg/pro), knowledge in materials management
  • Good knowledge in change management, workflow design, electronic approval process and Bill of Materials process
  • Good knowledge in business intelligence, data analytics and report generation
  • Familiarity with corrective and preventive Action (CAPA), Device master records (DMR), Design history file (DHF) and QMS concepts
  • Effective verbal and written communication skills to interact with international associates
  • Ability to prioritize responsibilities and ensure deadlines are met
  • Working knowledge of entire software development and test cycle with regulated Medical or Healthcare industry
  • Knowledge in international regulations and standards ISO, FDA and TUV.

Interested candidates may apply by clicking "Apply Online" below with a comprehensive CV stating academic qualifications, personal details, detailed experiences, personal contact details, names & contacts of 2 referees, current & expected salary. Candidates who do not provide the details as requested herein will not be considered.

If you think you have the right qualification and the skills for this Job, do not hesitate to send us your application by clicking on the "Apply Now" below.

"Only shortlisted candidates who meet our requirements will be notified"


Closing Date: 5 February 2012

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