Senior Medical Device Packaging Engineer - Cross-Site Leader

Brooksource

New Brighton (MN)

On-site

USD 76,000 - 90,000

Full time

14 days+
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Benefits offered by this job

Competitive benefits
401k with company match
Paid time off
Paid holidays
Employee Assistance Program

Job summary

Brooksource in New Brighton, MN is seeking a Senior Packaging Engineer to lead design, development, and validation of packaging for medical devices. You will ensure regulatory compliance across sites, mentor junior engineers, and collaborate with R&D, Regulatory, Quality, and Manufacturing teams.

The role focuses on sterile/non-sterile packaging, transit tests, shelf-life, seal integrity, and ongoing sustainability initiatives.

Qualifications

  • Bachelor's degree in Packaging Engineering, Mechanical Engineering, Biomedical Engineering, or related field.
  • 5+ years of packaging engineering experience in medical devices, pharma, or life sciences.
  • Experience with sterile barrier systems, validation, and regulatory compliance (ISO 11607, FDA QSR, EU MDR).
  • Proven ability to lead cross-functional packaging projects from concept through commercialization.

Responsibilities

  • Lead design, development, and qualification of sterile and non-sterile packaging for new products and line extensions.
  • Serve as technical lead across R&D, Regulatory, Quality, Manufacturing, and Supply Chain.
  • Develop and execute packaging validation protocols per ISO 11607, FDA/EU requirements.
  • Provide mentorship to junior engineers and cross-site teams.

Skills

Packaging engineering
Sterile packaging
Regulatory compliance
Cross-functional leadership
SolidWorks
Statistical analysis

Education

Bachelor's degree in Packaging Engineering or related

Tools

SolidWorks
Minitab
JMP

Job description

Brooksource in New Brighton, MN is seeking a Senior Packaging Engineer to lead design, development, and validation of packaging for medical devices. You will ensure regulatory compliance across sites, mentor junior engineers, and collaborate with R&D, Regulatory, Quality, and Manufacturing teams.

The role focuses on sterile/non-sterile packaging, transit tests, shelf-life, seal integrity, and ongoing sustainability initiatives.

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