Back to Search

Product Data Specialist

Date Posted: 9/14/2017

Apply Now

Job Description

A large, global medical device company in Irvine has an opportunity for a Product Data Specialist.
This position is an important individual contributor role in the TMVR department. The primary responsibility of this job is to plan and manage the configuration of documentation and parts associated with developing and manufacturing product data (DMR) throughout the product life cycle. This person will assist in and coordinate the creation and release of product information through the PLM system. He/she will drive timely release of change request according to project schedules through interaction with technical content owners and approvers from many levels of the organization as well as communicate status of documentation and parts configuration to engineers and project managers.
Responsibilities include:

  • Collaborate with engineers to create change request packages (ECRs) and assess impact of the proposed change by performing thorough impact assessments.
  • Initiate and facilitate change request in compliance with applicable procedures that support compliance with regulations and standards pertaining to EW quality system change management.
  • Assign part and processes numbers and assist internal customers in document formats, style, etc.
  • Responsible for data entry integrity when transferring changes to product data in multiple systems.
  • Responsible for ensuring that the best practices of Part/Document Change Management are followed.
  • Monitor parts and documents changes management process effectiveness and contribute to problem solving/continual improvement discussions with regard to change control process, including the impact of changes and takes the initiative to recommend process improvements.
  • Participate in department meetings and performs other tasks and related duties as assigned.
  • Super User for PLM Ignite
  • Proficient and in PLM and ERP systems
  • Participates in continuous process improvements focused on systems and reporting
  • Ensuring compliance with department and company procedures

work experience requirements
Technical and professional competencies for this position are as follows:
  • Associates degree required along with at least 2- 3 years of work experience
  • Requires a minimum of 1 years of experience in the Medical device or Pharma industry or automotive or aerospace
  • Has worked as a Documentation Specialist in Manufacturing or Engineer Tech, or Quality Tech
  • Will understand product structure and Item Master and Bills of Materials and routers
  • Must understand change process in a controlled fashion
 


 
  We are an equal opportunity employer.

Job Requirements

Associates degree required along with at least 2- 3 years of work experience

Requires a minimum of 1 years of experience in the Medical device or Pharma industry or automotive or aerospace

Has worked as a Documentation Specialist in Manufacturing or Engineer Tech, or Quality Tech

Will understand product structure and Item Master and Bills of Materials and routers

Must understand change process in a controlled fashion
Posted By: nphillips@ultimatestaffing.com

Apply Now Send to a Friend

Job Snapshot

  • Employee Type:Full-Time
  • Location:Irvine, CA
  • Job Type:Pharmaceutical
  • Experience:Not Specified
  • Education:Not Specified
  • Date Posted:9/14/2017
  • Contact: Nicole Phillips (949) 250-3511
  • Pay Range: $0.00 - $0.00 Annually
Get Job Alertsby Email
  • Receive alerts with new job opportunities that match your interests
  • Receive relevant communications and updates from our organization

Sign Up Now


Job Reference: JO-1709-9702