Advanced Research Associate: GMP & Process Innovation

Research & Diagnostic Systems, Inc.

Saint Paul (MN)

On-site

USD 50,000 - 82,000

Full time

14 days+

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Benefits offered by this job

Competitive benefits (medical, dental,
401k and ESPP
HSA and FSA
Tuition reimbursement
Mentorship and development
Volunteer time off
Parental leave

Job summary

Bio-Techne is seeking an Advanced Research Associate to support the development and sustained manufacture of its diverse product portfolio. The role involves executing SOPs, facilitating controlled experiments, and collaborating across functions to advance new and existing products.

The candidate will implement process improvements, ensure quality compliance, and contribute to operational excellence in a fast-paced environment.

Qualifications

  • Education and GMP laboratory experience required.
  • Experience in manufacturing or GMP setting preferred.
  • Strong documentation and data-analysis skills.

Responsibilities

  • Author, revise, and execute SOPs for manufacturing reagents and consumables.
  • Facilitate moderately complex controlled experiments to support new product development.
  • Perform validation activities for equipment used in GMP manufacturing processes.
  • Follow GDP to capture results, analyze data, and prepare reports.
  • Identify and resolve manufacturing process issues and lead troubleshooting.

Skills

GMP GDP knowledge
Data analysis
Communication
Organization
Independent & collaborative work
Fermentation knowledge

Education

Bachelor’s degree with 3–5 years relevant experience
Master’s degree with up to 2 years relevant experience

Tools

Microsoft Word
Microsoft Excel
Microsoft PowerPoint

Job description

Bio-Techne is seeking an Advanced Research Associate to support the development and sustained manufacture of its diverse product portfolio. The role involves executing SOPs, facilitating controlled experiments, and collaborating across functions to advance new and existing products.

The candidate will implement process improvements, ensure quality compliance, and contribute to operational excellence in a fast-paced environment.

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