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Packaging Engineer II

Abbott

Plymouth, MNFull-time$97–123K/yrSeen 4w ago

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At a glance

Compensation
$97–123K/yr
Location
Plymouth, MN
Schedule
Full-time
Work Authorization
Not specified

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Requirements

Credentials this posting asks for.

Bachelor's degree

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

RequiredNice to have

Skills

Process FMEAPackaging DesignPackaging ValidationLabeling Equipment ValidationDocumentation ManagementChange Request ManagementGood Manufacturing PracticesFDA 21 CFR 820ISO 13485ISO 11607ISO 20417

Qualifications

Bachelor's in EngineeringMaster's in Engineering or Equivalent2+ Years Professional Engineering Experience

Benefits

Medical Insurance
Dental Insurance
Paid Time Off
Tuition Assistance
401(k) Match

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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