
Duties and Responsibilities:
- Evaluate potential packaging materials to align both client and regulatory requirements (ie. USP, EP, ISO11607, ISO13485, EPR, PPWR, etc.)
- Evaluate packaging materials (secondary packaging materials/clean room sleeve) that protect closed-process systems against mechanical stress and cold storage
- Identify and develop a range of packaging sizes to meet the needs of the clients’ customers
- Identify and recommend testing methods to support design verification and validation, materials evaluation, vendor qualification, and packaging validation.
- Make recommendations for automated secondary packaging solutions to scale as needed
- Process optimization focused on making recommendations to improve packaging line efficiency, reduce scrap, and enhance robustness, increase sustainability etc.
- Must have strong hands on understanding of aseptic packaging, sterile barrier systems, and materials
- Ability to evaluate different materials, sizes, volumes, and packaging systems at a variety of mechanical stresses and temperatures (ie ambient, -80C)
- Skilled in materials science, mechanical properties, barrier performance, and failure mechanisms
- Able to create and recommend testing protocols consistent with industry standards
- Able to design and troubleshoot IOPQ protocols, transit simulations, and cryogenic stress tests
- Comfortable navigating regulatory documentation including, but not limited to: USP, EP, ISO11607, ISO13485, EPR, PPWR, and other global packaging standards
- Skilled in FMEA, hazard analysis, and root‑cause investigations
- Able to evaluate supplier data, challenge assumptions, and qualify new materials or components
- Familiar with thermal modeling, shipper qualification, and temperature‑excursion mitigation
- Must have strong documentation and communication skills
- Must have a safety and compliance oriented mindset
Additional Skills & Qualifications
- BS, Master’s, or PhD degree in Packaging Engineering, Materials Science, Chemical Engineering, Mechanical Engineering, Biomedical Engineering, or related field.
- 5-10 years of experience in in packaging engineering, ideally in biologics, cell therapy, gene therapy, or sterile pharmaceuticals
- Experience with aseptic fill-finish operations, cryogenic storage systems, and packaging validation
- Experience with regulatory documentation including, but not limited to: USP, EP, ISO11607, ISO13485, EPR, and PPWR
- (Preferred) experience with global regaulatory submissions
This is a Contract position based out of Minneapolis, MN.
Pay And Benefits
The pay range for this position is $52.00 - $58.00/hr.
Requirements
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)
This is a fully remote position.
Application Deadline
This position is anticipated to close on May 27, 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
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.
About the company
Company website•Business Consulting and Services
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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Our expertise spans capabilities in engineering including product and manufacturing, systems and software, construction management, environmental, architecture and civil; and power and utilities. We focus on sciences capabilities in laboratory sciences, healthcare, and clinical research.
Actalent is an operating company of Allegis Group, the global leader in talent solutions.








