Packaging Engineer

Stark Pharma Solutions Inc

Mansfield, MA

JOB DETAILS
SKILLS
Analysis Skills, Biology, Biotech and Pharmaceutical, Code of Federal Regulations, Continuous Improvement, Cross-Functional, Data Analysis, Design Verification, Documentation, Engineering, Ethylene, FDA (Food and Drug Administration), ISO (International Organization for Standardization), Laboratory Testing, Leadership, Maintain Compliance, Material Science, Mechanical Engineering, Medical Equipment, Performance Testing, Problem Solving Skills, Process Improvement, Process Validation, Product Development, Product Lifecycle, Product Packaging, Product Support, Product/Service Launch, Project Management Software, Project/Program Coordination, Project/Program Management, Quality Assurance, Quality Assurance Methodology, Regulations, Regulatory Compliance, Requirements Management, Research & Development (R&D), Risk Analysis, Root Cause Analysis, Sample/Specimen Processing, Statistics, Sterilization, Sustainability, Technical Writing, Test Data, Test Lab, Test Plan/Schedule, Testing, Validation Testing
LOCATION
Mansfield, MA
POSTED
5 days ago

Hi,

My name is Karthik Mutyala, and I am a Recruitment Manager with Stark Pharma Solutions, specializing in opportunities across the Pharmaceutical, Biotechnology, Medical Device, and Life Sciences industries.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.

Role: Packaging Engineer III (Medical Devices)

Location: Mansfield, MA

Duration: Long Term

Position Overview

We are seeking an experienced Packaging Engineer III to support product development, packaging design, validation, and commercialization activities for sterile and non-sterile medical devices. This role will lead packaging initiatives across new product introductions (NPI), sustaining engineering, and continuous improvement projects while collaborating with cross-functional teams in a regulated medical device environment.

The ideal candidate will have strong expertise in medical device packaging, package validation, and sterilization processes, with specific knowledge of EO (Ethylene Oxide) sterilization interactions with packaging systems.

Key Responsibilities

Packaging Development & Design

  • Lead the design, development, validation, and implementation of packaging systems for sterile and non-sterile medical devices.
  • Define packaging requirements related to functionality, safety, manufacturability, regulatory compliance, sustainability, and business objectives.
  • Collaborate with R&D, Quality, Regulatory, Operations, Labeling, and suppliers throughout the product lifecycle.
  • Support new product development, product transfers, and packaging improvements.

Verification & Validation

  • Develop and execute package validation strategies, including Design Verification (DV), Design Validation (DVal), and Packaging Process Validation activities.
  • Author test plans, protocols, reports, IQ/OQ/PQ documentation, and technical specifications.
  • Conduct package performance testing, data analysis, and statistical evaluations.
  • Support packaging equipment qualification and process characterization activities.

Packaging Testing & Compliance

  • Assist with operation of the package testing laboratory, including sample preparation, testing, and reporting.
  • Ensure compliance with FDA, ISO, ASTM, and ISTA packaging standards.
  • Perform risk assessments and root cause investigations related to packaging performance.
  • Maintain packaging documentation and Design History File (DHF) deliverables.

Project Leadership

  • Lead packaging workstreams within cross-functional development teams.
  • Coordinate project schedules, tooling requirements, equipment needs, and supplier activities.
  • Drive continuous improvement initiatives focused on quality, cost, efficiency, and standardization.

Required Qualifications

  • Bachelor's degree in Packaging Engineering, Mechanical Engineering, Materials Science, or related technical discipline.
  • 5+ years of packaging engineering experience within the medical device industry.
  • Strong knowledge of sterile barrier systems, thermoform trays, pouches, sealing technologies, and packaging materials.
  • Experience supporting EO sterilization and understanding its impact on packaging systems.
  • Hands-on experience with packaging validation, package testing, and process qualification activities.
  • Knowledge of:
  • ISO 11607
  • FDA 21 CFR Part 820
  • ISO 13485
  • ASTM & ISTA Packaging Standards
  • Experience developing technical specifications and engineering documentation.
  • Strong analytical, project management, and problem-solving skills.

About the Company

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Stark Pharma Solutions Inc