Packaging & Labeling Manufacturing Engineer II

Anteris Technologies; Maple Grove (MN); On-site; USD 90,000 - 110,000; Full time

Benefits offered by this job

Medical, Dental, Vision

401k + Company Match

Life, AD&D, STD/LTD

Bonus Plan Eligibility

Employee Equity Program

Paid Holidays & Vacation

Employee Assistance Program

Job summary

Anteris Technologies, a global structural heart company, is seeking a Manufacturing Engineer II in Minnesota to drive packaging and labeling process improvements. You will partner across Quality, Regulatory, R&D, and Production to ensure GMP-compliant, scalable packaging solutions for clinical products.

The role requires hands-on manufacturing engineering with 2+ years in medical device packaging, proficiency in 3D CAD (SolidWorks), and strong technical writing.

Qualifications

• BS with 2+ years in medical device manufacturing or MS with 1+ years.
• Experience in product packaging and labeling.
• Knowledge of statistics, quality systems and regulatory requirements.
• Collaborative, works with minimal supervision.
• Strong technical writing and documentation skills.
• Proficient in 3D CAD (SolidWorks) and labeling tools.

Responsibilities

• Serve as the Manufacturing Process SME for packaging and labeling.
• Provide day-to-day production support to ensure GMP compliance.
• Develop and maintain manufacturing documentation.
• Own process risk documentation and assist in risk analysis.
• Co-own 50+ packaging and labeling specifications.
• Support schedules with Supply Chain, QA, Regulatory, R&D.

Skills

Packaging

Labeling

GMP Compliance

Statistics

MS Office

3D CAD (SolidWorks)

Problem Solving

Communication

Education

Bachelor's degree or higher in relevant field

Packaging Engineering degree preferred

Tools

Bartender

Labelview

Easylabel

GS1 labeling

Job description

Anteris Technologies, a global structural heart company, is seeking a Manufacturing Engineer II in Minnesota to drive packaging and labeling process improvements. You will partner across Quality, Regulatory, R&D, and Production to ensure GMP-compliant, scalable packaging solutions for clinical products.

The role requires hands-on manufacturing engineering with 2+ years in medical device packaging, proficiency in 3D CAD (SolidWorks), and strong technical writing.