Packaging Engineer; EUMDR, Design Control

Position

Packaging Engineer (Must Have EUMDR, Design Control)

Franklin Lakes, NJ or Vernon Hills, IL or Salt Lake City, UT

6 Months

40.00

Medical Device Company

Engineering

Packaging COE (R&D)

Mid-Level

Contract on W2 (Need US Citizens or GC Holders Only)

• Franklin Lakes, New Jersey
• Vernon Hills, Illinois
• Salt Lake City, Utah

• Packaging design development for medical devices or pharma industry
• Packaging verification and validation for medical devices or pharma industry
• Design control process for medical devices
• CAD tools for packaging design
• Packaging standards and regulatory requirements for medical devices (i.e., ISO
  11607, EUMDR, etc.)

• Bachelor Degree equivalent in Packaging, Mechanical Engineering, Materials Engineering or in a related field of study.

• minimum 2 years of experience in Medical Device packaging

• Demonstrates working knowledge of package engineering principles and techniques
• Demonstrates working knowledge of legal requirements and documents.
• Designs, prototypes and qualifies standard new packaging concepts in accordance with design control requirements with moderate guidance.
• Evaluates and improves standard existing packaging concepts with moderate guidance.
  
  Identifies, analyzes and specifies standard packaging materials and equipment with moderate guidance.
• Supports external resource/contractors as required.
• Has developed knowledge and skills in packaging; still acquiring / expanding fundamental knowledge and higher-level skills.
• Applies knowledge and skills to a variety of standard activities.
• Works with moderate guidance in own area of knowledge.

• Effectively communicates technical knowledge and validates understanding of other packaging test methods/standards and related equipment.
• Medical device packaging system development for flexible and rigid packaging applications.
• Packaging system verification and validation experience
• Experience/knowledge with CAD tools for packaging design
• Experience with statistics and design of experiments.
• Knowledge of the following standards: ISO 11607, ISO 13485, ISO 14971

• Will not manage any direct reports.
• Will not be responsible for any functional areas.
• Knowledgeable and adherent to client Quality and Corporate Policies.