Packaging Engineer

Millenniumsoft•Covington, GA

6d•Onsite

About The Position

We are seeking a Packaging Engineer with FDA regulatory experience for a contract position in Covington, GA. This role involves the validation and testing of commercial package designs, recommending appropriate packaging materials and equipment, and developing prototypes. The engineer will also be responsible for designing/re-designing tooling and fixturing, utilizing various analysis techniques, and working with vendors to meet packaging requirements. This position requires detailed documentation of activities and active participation in project team meetings and design reviews.

Requirements

Proven ability to design/re-design existing commercial packaging
Proficient in the use of a personal computer with intermediate keyboarding skills and proficiency in the use of Microsoft Word, Excel, PowerPoint, Access, Microsoft Project, and various statistical software packages.
BS in Packaging Engineering or related field of study
Minimum 2 years experience or relevant experience
Regulated industry experience a plus
Microsoft Word, Excel, Project, PowerPoint and Access

Nice To Haves

FDA regulatory experience

Responsibilities

Validation and testing of commercial package design and any modifications to existing package design.
Recommends appropriate packaging equipment, tooling, and/or materials to meet regulatory requirement for package testing.
Converts customer/regulatory needs into existing package design.
Develops prototypes of concepts and subcomponent mechanisms.
Designs/re-designs and develops tooling and fixturing required to support existing or package design/re-design.
Utilizes design concepts and analysis techniques, including but not limited to: Failure Mode Analysis, Finite Element Analysis & modeling, Geometric Dimensioning, Statistical Analysis, Tolerancing Analysis, Stress/Strain Analysis.
Works with vendors and customers to identify appropriate materials and components to meet packaging requirements.
Analyzes existing design to ensure that the specifications (Product Performance Specifications) meet the customers’ and/or regulatory requirement.
Ability to detail re-designs to ensure manufacturability; proper dimensioning and tolerances stack-up analysis. Recommends modifications as required.
Establishes and maintains appropriate documentation of activities in accordance with existing policies and procedures (Divisions, Corporate, and Regulatory compliance).
Actively participates on MDR project team meetings and/or Design Reviews.