Packaging Engineer II

Job Title: Packaging Engineer II Job Description
We are seeking a Packaging Engineer II to join our team and support packaging development activities for medical devices. This role involves owning packaging projects from concept through validation, ensuring compliance with regulatory requirements and internal quality standards. The successful candidate will support packaging system design, validation activities, design controls, risk management, labeling, and manufacturing support. A strong project management skill set, documentation ownership, and the ability to work cross-functionally throughout the product development lifecycle are essential.
Responsibilities
- Own and manage packaging projects from concept through validation.
- Ensure compliance with regulatory requirements and internal quality standards.
- Support packaging system design and validation activities.
- Manage design controls, risk management, labeling, and manufacturing support.
- Work independently on multiple projects simultaneously.
- Collaborate cross-functionally with engineering, manufacturing, quality, and regulatory teams.
Essential Skills
- Medical device packaging design experience, including sterile barrier systems and terminally sterilized products.
- Strong knowledge of ISO standards and packaging validation requirements.
- Experience owning documentation, design history files (DHF), testing protocols, and regulatory deliverables.
- Proficient with CREO for packaging design and drawing creation.
- Working knowledge of FDA Part 820, GMP requirements, risk management, and medical device design controls.
- Experience with steam sterilization packaging systems, ASTM standards, Six Sigma, ISTA testing, and labeling development.
Additional Skills & Qualifications
- Bachelor’s Degree in Packaging Engineering, Mechanical Engineering, Biomedical Engineering, or a related field.
- 2+ years of packaging engineering experience preferred.
- Experience developing packaging systems for terminally sterilized medical devices.
- Knowledge of ISO Part 1 and Part 2 requirements.
- Experience with packaging validation protocols and reports.
- CREO proficiency and 3D design skills.
- Strong technical writing and documentation skills.
- Experience with steam sterilization cases and trays.
- Knowledge of EU MDR requirements.
- Experience supporting regulatory remediation projects.
- Six Sigma or DFSS experience.
- Minitab experience.
Work Environment
The position is based onsite in a Memphis area facility, requiring four days onsite per week for a total of 40 hours per week. The work environment is a collaborative engineering and manufacturing setting, involving cross-functional interaction with Quality, Regulatory, Manufacturing, and R&D teams. It is a fast-paced project environment supporting multiple product lines and remediation initiatives.
Job Type & Location
This is a Contract position based out of Memphis, TN.
Pay and Benefits
The pay range for this position is $45.00 - $60.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors. Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Memphis,TN.
Application Deadline
This position is anticipated to close on Sep 28, 2026. About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.

If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email [email protected] for other accommodation options.

San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.

Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.