Integra LifeSciences

Product Lifecycle Management (PLM) Specialist

Vacancy ID
2017-22350
Location
FR-Saint Priest
Position Type
Regular Full-Time
Category
Information Technology

Overview

Integra LifeSciences, a world leader in medical technology, is dedicated to limiting uncertainty for surgeons, so they can concentrate on providing the best patient care. Integra offers innovative solutions in orthopedic extremity surgery, neurosurgery, reconstructive and general surgery, and regenerative wound care.  Founded in 1989 Integra is headquartered in Plainsboro, New Jersey and has nearly 4,000 employees worldwide. Integra's common stock is listed on The NASDAQ Stock Market under the symbol "IART."

 

Integra LifeSciences has entered into an acquisition agreement of Codman Neurosurgery.   This transformational acquisition creates compelling value for our shareholders, employees and patients, and enhances our global position in neurosurgery by adding a complementary product portfolio and the world-recognized Codman brand. This expansion position is open as a result of this exciting acquisition.

 

SUMMARY DESCRIPTION       

 

Responsibilities

 

ESSENTIAL DUTIES AND RESPONSIBILITIES

 

  • Partner with functional leaders on business requirements cross functional work streams (Oracle Manufacturing, Oracle Order to Cash …)
  • Work on product master data (parts, documents, drawings, Bills of Material, and related information) with Business teams
  • Work on deploying new functionalities or improvement
  • Assist end users (change management, training, support …)
  • Support documentation/Validation processes (FDA CFR Part 11 related)

 

Qualifications

QUALIFICATIONS:

  • Experience in Documentation Control, Engineering, and/or Product Management (BOMs, Routings, Change Orders)
  • 3-5 years of experience participating in cross-functional projects
  • Very comfortable with computers, with concepts, with data sets manipulations (SQL, Excel, …)
  • Comfort working in a regulated environment is a plus: FDA Quality Systems and Design Controls (21 CFR 820.30, ISO 13485, Part 11) and other related medical device regulations preferred
  • Medical devices or technology experience is a plus
  • Product Life Cycle Management/ERP software experience; Oracle/Agile PLM experience preferred

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