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Manufacturing Engineer

Bio-Techne
Minneapolis, MN Full Time
POSTED ON 6/27/2026 CLOSED ON 8/12/2026

What are the responsibilities and job description for the Manufacturing Engineer position at Bio-Techne?

By joining Bio-Techne, you’ll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide.

Pay Range

$55,600.00 - $91,450.00

Position Summary:

The Manufacturing Engineer supports the development, improvement, and troubleshooting of manufacturing processes, including both mechanical and chemical operations. Working under the guidance of senior engineers, this role contributes to automation projects, helps maintain process documentation, and assists in daily production support to ensure quality, safety, and efficiency. 

Key Responsibilities:

Process Support & Improvement

  • Assist in developing and updating manufacturing processes, work instructions, and SOPs. 
  • Help perform basic time studies, process mapping, and data collection. 
  • Support efforts to identify inefficiencies and implement continuous improvements. 

Automation Support

  • Assist in the installation, testing, and troubleshooting of automated equipment (robots, PLC-controlled systems, sensors). 
  • Work alongside senior engineers and integrators to support automation upgrades and process optimization. 
  • Participate in equipment validation activities such as FAT/SAT and IQ/OQ tasks under supervision. 

Chemical Process Support

  • Support chemical mixing, dispensing, coating, curing, and related operations within production. 
  • Assist with monitoring chemical process parameters, documenting results, and ensuring compliance with safety procedures. 
  • Help maintain chemical handling instructions, cleaning procedures, and related process documentation. 

Quality & Compliance

  • Support investigations for nonconformances by gathering data and helping execute corrective actions. 
  • Participate in PFMEA reviews, risk assessments, and process validations led by senior staff. 
  • Follow GMP/IVD/ISO 13485 or similar regulatory requirements as applicable. 

Daily Production Support

  • Provide hands-on support to operators and technicians on equipment, materials, or process questions. 
  • Help troubleshoot basic equipment or process issues before escalating. 
  • Monitor production metrics such as scrap, yield, and cycle time. 

Documentation & Reporting

  • Update process documents, equipment logs, and engineering records in collaboration with senior engineers. 
  • Collect and analyze basic production data to support engineering reports. 
  • Maintain accurate documentation related to automation, chemical processes, and process improvements. 

Qualifications

Education and Experience:

  • Bachelor’s degree in manufacturing, Chemical, Mechanical, Industrial Engineering, or related field. 
  • Internship or 0–2 years of experience in a manufacturing, chemical, or engineering environment. 
  • Experience in the pharmaceutical, life sciences, or med device industries is a plus
  • Basic understanding of manufacturing processes, chemical handling, or automation systems. 
  • Familiarity with CAD tools (SolidWorks, AutoCAD, etc.). 
  • Strong analytical, problem-solving, and hands-on technical skills. 

Knowledge, Skills, And Abilities

  • Exposure to automation (robotics, PLCs, sensors) through coursework, internships, or projects. 
  • Experience in regulated industries (Medical Device, IVD, Pharma, Aerospace) is a plus. 
  • Understanding of Lean/6σ concepts or participation in improvement projects. 
  • Basic familiarity with Minitab, JMP, or other data analysis tools. 
  • Willingness to learn and develop technical skills. 
  • Strong attention to detail and documentation. 
  • Ability to work effectively with cross-functional teams. 
  • Good communication and interpersonal skills. 
  • Problem-solving mindset with curiosity for how things work. 

Working Conditions

  • Primarily on-site at Bio-Techne’s Minneapolis facility.
  • May require occasional extended hours to meet project deadlines.

Physical Requirements

  • Ability to work hours that conform to standard business operations
  • Ability to sit or stand for extended periods
  • Occasional lifting materials up to 5-50 lbs.
  • Use of computer and office equipment

Why Join Bio-Techne

  • We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield.
  • We invest in our employees’ financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA.
  • We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more.
  • We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging.
  • We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave.
  • We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table.

Bio-Techne is an E-Verify Employer in the United States.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.

Salary : $55,600 - $91,450

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