
Packaging Engineer II
Plymouth, MNFull-time$97–123K/yrSeen 4w ago
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Job overview
Abbott is hiring a Packaging Engineer II. The Packaging Engineer II at Abbott in Plymouth, MN will develop and validate packaging and labeling for new medical device products, design and test packaging solutions, manage documentation, and support equipment procurement while ensuring compliance with GMP, FDA, and ISO standards.
Key focus areas include Develop and validate packaging and labeling for NPI projects, Design, develop, and test packaging for protection, display, and handling of medical devices, and Support selection, procurement, installation, and validation of packaging and labeling equipment.
Important skills include Process FMEA, Packaging Design, Packaging Validation, Labeling Equipment Validation, Documentation Management, and Change Request Management.
Skills & qualifications
Skills
Qualifications
Benefits
Full job description
Job Duties
PACKAGING ENGINEER II – St. Jude Medical, an Abbott Labs Co. / Plymouth, MN
Responsible for developing and validating packaging and labeling for New Product Introduction (NPI) projects. Design, develop, and test packaging used for the protection, display, and handling of medical device products. Support the selection, procurement, installation, and validation of packaging and labeling equipment. Conduct Process FMEAs and identify and implement packaging and labeling process improvement projects. Determine packaging specifications according to the nature of the product, cost limitations, legal requirements, and the type of protection required, considering need for resistance to such external variables as moisture, corrosive chemicals, temperature variations, light, heat, rough handling, and tampering. Responsible for selecting and procuring packaging and labeling materials from vendors. Assist in designing package exteriors considering such factors as product identification, sales appeal, aesthetic quality, printing and production techniques. Responsible for documentation management and an understanding of Good Manufacturing Practices (GMPs). Manage and create change requests within the document control system. Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and support medical device manufacturing regulatory requirements, including FDA 21 CFR 820 and ISO 13485, 11607 and 20417. Comply with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments.
Bachelor’s or foreign equivalent degree in an Engineering field of study with at least 2 years of related professional engineering experience. In the alternative, will accept a Master’s or foreign equivalent degree. Each alternative requirement must include an academic or industrial background in: (i) designing, developing, and testing packaging used for the protection, display, and handling of medical device products; (ii) conducting Process FMEAs and identify and implement packaging and labeling process improvement projects; (iii) documentation management and an understanding of Good Manufacturing Practices (GMPs); and (iv) supporting medical device manufacturing regulatory requirements, including FDA 21 CFR 820 and ISO 13485, 11607 and 20417. Employer will accept any suitable combination of education, training, experience.
An EOE. 40 hrs/wk. $96,928 - $122,700/year. Send resumes to [email protected] or by mail to Abbott Laboratories, Attn: 26J14A, Willis Tower, 233 S. Wacker Dr., Floor 26, Dept. 32, Chicago, IL 60606. Refer to ad code: SJM-0081-ES
Minimum Education Required
Bachelor’s or foreign equivalent degree in an Engineering field of study with at least 2 years of related professional engineering experience. In the alternative, will accept a Master’s or foreign equivalent degree. Employer will accept any suitable combination of education, training, experience.
Minimum Experience Required
Each alternative requirement must include an academic or industrial background in: (i) designing, developing, and testing packaging used for the protection, display, and handling of medical device products; (ii) conducting Process FMEAs and identify and implement packaging and labeling process improvement projects; (iii) documentation management and an understanding of Good Manufacturing Practices (GMPs); and (iv) supporting medical device manufacturing regulatory requirements, including FDA 21 CFR 820 and ISO 13485, 11607 and 20417.
Shift
First (Day)
Number of Openings
1
Public Transportation Accessible
Yes
Compensation
$96,928.00 - $122,700.00 / Annually
Postal Code
55442
Job Type
Full Time
Place of Work
On-site
Requisition ID
SJM-0081-ES
Job Benefits
Medical Insurance
Retirement Plan
401(k)
Tuition Reimbursement
Dental
Vision
Holidays, PTO, Sick Days
Life Insurance
Application Instructions
Send resumes to [email protected] or by mail to Abbott Laboratories, Attn: 26J14A, Willis Tower, 233 S. Wacker Dr., Floor 26, Dept. 32, Chicago, IL 60606. Refer to ad code: SJM-0081-ES
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