1

Aseptic Process Engineer Jobs in Minnesota (NOW HIRING)

Strong knowledge of microbiological techniques and aseptic processing Travel * N/A Safety: Physical Requirement * Move or lift objects up to 25 pounds * Frequent (>75%) stationary position (standing ...

Responsibilities / Tasks GEA Group, founded in Germany in 1881 , is a global leader in engineering ... Knowledge of beverage processing systems such as UHT, pasteurization, aseptic processing ...

Field Service Technician

Afton, MN · On-site

$31 - $45/hr

Responsibilities / Tasks GEA Group, founded in Germany in 1881 , is a global leader in engineering ... Knowledge of beverage processing systems such as UHT, pasteurization, aseptic processing ...

Responsibilities / Tasks GEA Group, founded in Germany in 1881 , is a global leader in engineering ... Knowledge of beverage processing systems such as UHT, pasteurization, aseptic processing ...

Daybreak Assistant

Willmar, MN · On-site

$15.76 - $17.75/hr

Well-developed team work process within the department and with all other departments within the ... Assisting with client care and programming. Tasks: * Clients are treated with care and respect.

Showing results 21-28

Aseptic Process Engineer information

See Minnesota salary details

$34.8K

$89.5K

$133.8K

How much do aseptic process engineer jobs pay per year?

As of Sep 5, 2026, the average yearly pay for aseptic process engineer in Minnesota is $89,511.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,700.00 and $100,900.00 per year, depending on experience, location, and employer.

What is an aseptic process engineer?

Aseptic process engineers are professionals who design, develop, and maintain sterile manufacturing systems, primarily in the pharmaceutical, biotechnology, and food industries. Their main responsibility is to ensure that products are produced in a contamination-free environment, using processes that prevent the introduction of microorganisms. This involves overseeing the design of cleanrooms, validating equipment, developing standard operating procedures, and ensuring regulatory compliance. Aseptic process engineers work closely with quality assurance teams to maintain high standards of product safety and efficacy. Their expertise is crucial for industries where product sterility is critical to consumer safety.

What are the key skills and qualifications needed to thrive as an aseptic process engineer, and why are they important?

Aseptic Process Engineers need a strong background in chemical, mechanical, or biomedical engineering, along with experience in aseptic manufacturing environments and a solid understanding of GMP regulations. Familiarity with process automation systems, sterilization equipment, and industry certifications such as Six Sigma or Lean Manufacturing are often required. Attention to detail, strong problem-solving abilities, and effective communication are vital soft skills for ensuring product quality and process efficiency. These skills are crucial for maintaining sterile conditions, regulatory compliance, and the safe production of pharmaceuticals or biotechnology products.

What are some common challenges faced by aseptic process engineers, and how can they be addressed?

Aseptic Process Engineers often encounter challenges such as maintaining strict sterility standards, troubleshooting equipment issues, and ensuring compliance with changing regulatory requirements. Addressing these challenges requires strong attention to detail, proactive communication with cross-functional teams, and staying current with industry best practices and regulations. Collaborating closely with quality assurance, production, and maintenance teams helps to identify and resolve issues quickly, ensuring that processes remain efficient and compliant.

What is the difference between Aseptic Process Engineer vs Pharmaceutical Manufacturing Technician?

AspectAseptic Process EngineerPharmaceutical Manufacturing Technician
CredentialsBachelor's degree in engineering, life sciences, or related field; GMP trainingHigh school diploma or associate degree; GMP training often required
Work EnvironmentCleanroom, sterile environments, manufacturing facilitiesManufacturing floors, production areas, sometimes cleanrooms
Industry UsageDesign, optimize, and validate aseptic processes in pharmaOperate equipment, assemble products, support manufacturing

The Aseptic Process Engineer focuses on designing and validating sterile manufacturing processes, requiring specialized engineering knowledge. In contrast, the Pharmaceutical Manufacturing Technician handles day-to-day production tasks, often with less formal education but essential for maintaining manufacturing flow. Both roles are vital in pharmaceutical production but differ in responsibilities and qualifications.

What job categories do people searching Aseptic Process Engineer jobs in Minnesota look for?

The top searched job categories for Aseptic Process Engineer jobs in Minnesota are:

Infographic showing various Aseptic Process Engineer job openings in Minnesota as of August 2026, with employment types broken down into 100% Full Time. Highlights an 89% In-person, and 11% Hybrid job distribution, with an average salary of $89,511 per year, or $43 per hour.

Technical Support Specialist (Histology, Flow Cytometry,Cell Gene Therapy)

EXRE protein

Minneapolis, MN • On-site

$85 - $125/hr

Other

Posted 4 days ago


Key responsibilities

  • Provide advanced technical support for histology, flow cytometry, and cell therapy products and systems.

  • Conduct remote and on-site training sessions on equipment, protocols, and best practices for histology, flow cytometry, and cell culture.

  • Assist in the implementation, troubleshooting, and demonstration of complex workflows involving cell differentiation, characterization, and histopathological validation.


Job description

Senior Technical Support Specialist (Histology, Flow Cytometry, & Cell Gene Therapy)

Position Type: Full Time

Job Location: Minneapolis, MN

Position Summary

We are seeking a highly skilled Technical Support Specialist with a unique, cross‑functional expertise spanning histology, flow cytometry, and advanced cell culture systems. You will provide expert‑level support for our core portfolios: Dakewe histology solutions, flow cytometry systems, and our stem cell research & cell therapy product line (including GMP‑grade media, growth factors, cytokines, and differentiation kits). The ideal candidate will bridge the gap between basic research tools and therapeutic development, supporting customers from discovery through translational workflows. This role requires deep technical knowledge, excellent communication skills, and a passion for customer success across multiple, sophisticated technology platforms.

Essential Duties and Responsibilities Technical Customer Support
  • Provide advanced, integrated technical support for Exreprotein’s multi‑disciplinary portfolio:
  • Histology: Equipment, reagents, and consumables for tissue‑based analysis.
  • Flow Cytometry: Instrument operation, software, application support, and reagents for immunophenotyping and characterization.
  • Stem Cell & Cell Therapy: Growth factors, cytokines, basal media, feeds, and specialized supplements for pluripotent stem cell (iPSC/ESC) culture, directed differentiation, and primary immune cell expansion (e.g., T‑cells, NK cells) for therapeutic applications. Support includes protocol optimization, quality control testing interpretation, and scalability advice.
  • Troubleshoot complex, cross‑platform customer inquiries involving cell culture health, differentiation efficiency, characterization data (flow cytometry, IHC), and instrument performance.
  • Document all customer interactions and technical issues accurately in our CRM system.
  • Collaborate with internal R&D, QA, and manufacturing partners to escalate and resolve advanced technical and application‑specific issues.
Customer Training & Education
  • Histology/IHC: Equipment and staining protocols.
  • Flow Cytometry: Instrument operation, panel design, and analysis.
  • Advanced Cell Culture: Aseptic technique, media preparation, growth factor reconstitution/storage, cell line‑specific protocols, cryopreservation, and best practices for maintaining culture consistency and compliance.
  • Conduct remote and on‑site training sessions, with the ability to adapt content for both academic research labs and regulated cell therapy development environments.
  • Create and update technical documentation, application notes, and troubleshooting guides.
Field‑Based & On‑Site Support
  • Perform on‑site visits to provide hands‑on support across the portfolio.
  • Histology/Flow Cytometry: Instrument optimization and assay troubleshooting.
  • Cell Therapy Support: Assist in the implementation of media and growth factor systems, review of aseptic processes, and troubleshooting of cell expansion or differentiation protocols in R&D, process development, or GMP‑like settings.
  • Demonstrate new products and complex integrated workflows (e.g., from cell differentiation to flow analysis to histopathological validation).
Pre‑ & Post‑Sales Scientific Support
  • Work closely with the Sales team as a scientific expert for the entire portfolio, with a focus on consultative support for cell‑therapy and stem cell research customers.
  • Assist in experimental design, product selection, and protocol development for complex projects involving cell culture systems, characterization, and downstream analysis.
  • Build trusted advisor relationships with scientists, process development engineers, and lab directors in both research and biopharma.
Qualifications
  • Education: Advanced degree (M.S. or Ph.D.) in Cell Biology, Immunology, Stem Cell Biology, Bioengineering, or a closely related field is highly preferred.
  • Experience:
    • Histology: Practical experience (2+ years) in histology/IHC techniques and equipment. HT/HTL certification is a plus.
    • Flow Cytometry: Hands‑on experience (2+ years) operating cytometers and supporting multicolor panel applications for characterization.
    • Stem Cell/Cell Therapy: Minimum 3+ years of hands‑on experience with human pluripotent stem cell (iPSC/ESC) culture, directed differentiation, and/or primary immune cell culture for therapeutic applications (CAR‑T, TCR, NK cells). Direct experience with a variety of commercial media systems, growth factors, and matrices is required.
    • Experience in a GLP/GMP environment is a significant advantage.
  • Deep, integrated knowledge of Histology, Immunology, cell culture biology, stem cell protocols, and the critical role of growth factors/media in determining cell fate and function.
  • Ability to understand and support the unique needs of both research and process development labs moving toward clinical translation.
  • Strong technical aptitude for troubleshooting complex, multi‑step biological workflows and associated instrumentation.
  • Exceptional communication, teaching, and scientific presentation skills.
  • Self‑motivated, organized, and able to manage a complex international travel and support schedule.
  • Must possess a valid passport and driver’s license and be able to travel internationally without restriction.
Physical Demands and Work Environment
  • An employee, to successfully perform the essential functions of this position, requires extended sitting or standing at workstation or at desk.
  • The employee should be able to lift 50 pounds, if necessary.
  • Reasonable accommodations may be made to enable individuals with disabilities to perform the functions.
Note

This job description in no way states or implies that these are the only duties to be performed by the employee(s) of this position. Employees will be required to follow any other job‑related instructions and to perform any other job‑related duties requested by any person authorized to give instructions or assignments. All duties and responsibilities are essential functions and requirements and are subject to possible modification to reasonably accommodate individuals with disabilities.

#J-18808-Ljbffr