Pro Staff

Packaging Engineer

6 days left

Employer
Pro Staff
Location
Plymouth, MN
Posted
Jun 25, 2018
Closes
Jul 25, 2018
Ref
328284
Contact
Pro Staff
Category
Other
Job Type
Employee
Employment Status
Full Time
Atterro has partnered with Cantel Medical to bring on an experienced Packaging Engineer to help head a key project! As the Labeling Project Leader, you will be responsible for the overall coordination, development and execution of Global Labeling Projects for Cantel Medical. You will provide project leadership and orchestration of labeling development activities interfacing with Marketing, R&D, Regulatory, Technical Communications, Legal, Package Engineering and site Operations. The Labeling Project Leader will also support the development of solutions for labeling initiatives, including recommending activities involving various areas.

Hours: Regular Business Hours
Pay: Depends on Experience
Duration: 6+ months

Job Duties:

  • Creation of global standard and templates for new and existing products including product labeling, IFU’s and other forms of regulated packaging material
  • Monitors changes in labeling regulations in the US and/or abroad and ensures that labeling meets all medical, legal, and regulatory requirements
  • Ensures all requested projects have appropriate labeling resources assigned to enable on-time completion of project goals
  • Monitor, evaluate and recommend improvements to labeling processes, quality, systems tools and/or policies
  • Leads, directs, and reviews the work of a team who exercise latitude and independence in their assignments
  • Establishes operational plans and implements policies and strategies
  • Strive for continuous improvement and consistency in deliverables
  • Communicates with internal and external customers and vendors regarding ongoing operations
  • Uses information exchange, influence and active persuasion without direct exercise of command to gain cooperation of other parties
  • Requirements:
  • Four-year college science-related Degree 
  • Minimum of 3 years labeling experience, preferably in the following areas:
  • Developing labeling for medical devices for FDA and global markets.
  • Developing or improving documentation (e.g. SOPs) in an FDA regulated industry.
  • Strong interpersonal skills
  • Project Management Professional desired
  • Strong relationship management and communication skills, both oral and written
  • Customer orientation and ability to adapt/respond to different types of characters
  • Must be able to listen to the customer’s requirements, desires and concerns, and then recommend solutions
  • Self-motivated and able to work independently
  • Moderate Knowledge of medical device regulations and standards relating to labeling and regulated documentation
  • Action-oriented and customer-focused 
  • Ability to function well under pressure
  • Flexible to balance day-to-day delivery
  • Experience with content management, translation, labeling graphics design and proofreading systems desirable
  • Skills in Microsoft Word, Excel, PowerPoint, Outlook, and Microsoft Project

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