ackaging & Labelling Engineer
Published on CazVidat Siri Info Solutions Inc
Title : Packaging & Labelling Engineer Location – Franklin Lakes, NJ Duration : 6+ Months Job Description: Prior experience mandatory in the medical devices dom
Salary
$50 per hour
Location
Franklin Lakes, New Jersey, United States
Employment type
Full time
Workplace
Not provided
ackaging & Labelling Engineer
$50 per hour
Job description
Title : Packaging & Labelling Engineer Location – Franklin Lakes, NJ Duration : 6+ Months Job Description: Prior experience mandatory in the medical devices domain. Design and develop packaging systems compliant with ISO 11607-1 & 2. Author rationales, protocols, and strategies for packaging changes. Conduct and analyze packaging validation tests (seal strength, integrity, aging, distribution), hold design reviews. Manage sample builds and lead cross-functional design reviews. Prepare validation reports and maintain accurate documentation. Implement labelling changes using Adobe InDesign in compliance with regulatory requirements. Collaborate with Regulatory Affairs to ensure correct symbols, UDI, and multilingual content. Drive packaging and labelling projects independently, coordinating with manufacturing, quality, and regulatory teams.
Frequently asked questions
Do I need prior experience in the medical devices industry for this role?
Yes, you must have prior experience specializing in designing and developing packaging systems compliant with ISO 11607-1 & 2 standards in the medical devices industry.
Is this position remote or on-site?
This is an on-site position located in Franklin Lakes, New Jersey.
What are the main responsibilities for the Packaging & Labelling Engineer?
You will lead packaging validation tests, author protocols and strategic plans, manage sample builds, update labelling using Adobe InDesign, and collaborate with Regulatory Affairs and other teams.
What is the hourly pay for this job?
The position pays USD 50 per hour.
Will I be working with regulatory compliance and documentation?
Yes, you will prepare validation reports, maintain documentation for regulatory compliance, and work closely with Regulatory Affairs on labelling requirements.