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Intern St Jude Medical Device Jobs (NOW HIRING)

Abbott

Packaging Engineer II

Minneapolis, MN · On-site

$96K - $122K/yr

Job Duties PACKAGING ENGINEER II - St. Jude Medical, an Abbott Labs Co. / Plymouth, MN Responsible ... medical device products. Support the selection, procurement, installation, and validation of ...

Providence

Dermatologist

Yorba Linda, CA · On-site

$461K - $695K/yr

St. Jude Heritage Medical Group seeks a full-time Dermatologist to join its established team in beautiful Yorba Linda, California. You will be joining St. Jude Heritage Medical Group, an independent ...

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How much do intern st jude medical device jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for intern st jude medical device in the United States is $17.04, according to ZipRecruiter salary data. Most workers in this role earn between $14.42 and $19.23 per hour, depending on experience, location, and employer.

What does an intern at St. Jude Medical Device do?

An Intern at St. Jude Medical Device is typically involved in supporting engineering, research, or business teams by assisting with projects, data analysis, and process improvements. Interns gain hands-on experience with medical devices, participate in team meetings, and may contribute to product development or testing. The internship is designed to provide valuable industry exposure while developing relevant technical and professional skills.

What types of projects or tasks can an intern at St. Jude Medical Device expect to work on?

As an intern at St Jude Medical Device, you can expect to be involved in a variety of hands-on projects that support ongoing product development, quality assurance, or research initiatives. Interns often assist with data analysis, testing of medical devices, preparing technical documentation, and collaborating with cross-functional teams such as engineering, regulatory, and marketing. This role provides valuable exposure to the medical device industry, and you'll gain practical experience by contributing to real-world projects under the guidance of experienced professionals. The supportive environment encourages learning and growth, making it an ideal opportunity to develop industry-specific skills.

What are the key skills and qualifications needed to thrive as an intern at St. Jude Medical Device?

To thrive as an Intern at St. Jude Medical Device, you generally need a background in biomedical engineering, life sciences, or a related field, along with a strong academic record. Familiarity with laboratory equipment, data analysis software (such as MATLAB or Excel), and knowledge of regulatory standards like FDA guidelines are valuable. Attention to detail, willingness to learn, and effective communication skills help interns excel in collaborative, fast-paced environments. These skills and qualities are crucial for contributing to innovative projects, ensuring safety and compliance, and gaining meaningful hands-on experience in the medical device industry.

What is the difference between Intern St Jude Medical Device vs Intern Abbott Medical Devices?

AspectIntern St Jude Medical DeviceIntern Abbott Medical Devices
Required CredentialsEnrolled in biomedical, electrical, or related engineering programs; some technical certificationsSimilar educational background; certifications vary by role
Work EnvironmentManufacturing facilities, R&D labs, clinical settingsManufacturing plants, R&D centers, clinical support environments
Employer & Industry UsagePart of Abbott, focusing on cardiovascular devicesPart of Abbott, covering diverse medical device sectors

Both Intern St Jude Medical Device and Intern Abbott Medical Devices roles typically require students pursuing engineering or related degrees, with similar work environments in manufacturing and R&D. The main difference lies in the specific product focus: St Jude Medical specializes in cardiovascular devices, while Abbott Medical Devices covers a broader range of medical technologies within the same parent company.

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Intern St Jude Medical Device jobs near you
Infographic showing various Intern St Jude Medical Device job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $35,436 per year, or $17 per hour.

Packaging Engineer II

Abbott

Minneapolis, MN • On-site

$96K - $122K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

This job post has expired 2 days ago. Applications are no longer accepted.

Abbott rating

7.8

Company rating: 7.8 out of 10

Based on 138 frontline employees who took The Breakroom Quiz

170th of 545 rated manufacturers

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 AbbottJobs1@abbott.com 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 AbbottJobs1@abbott.com 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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