GMP Bioprocess Research Associate

biotechne

Saint Paul (MN)

On-site

USD 50,000 - 82,000

Full time

4 days ago
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Benefits offered by this job

Medical insurance
Dental insurance
Vision insurance
Life insurance
Short-term disability
Long-term disability
Pet insurance
ID shield

Job summary

Bio-Techne seeks an Advanced Research Associate to support the development and sustained manufacture of its diverse product portfolio. You will author, revise, and execute SOPs for reagents and consumables while facilitating controlled experiments to advance new products and implement process improvements.

In a fast-paced environment, you’ll ensure GDP compliance, perform data analyses, and collaborate with cross-functional teams to meet project objectives and maintain quality standards.

Qualifications

  • GMP laboratory experience required.
  • GDP knowledge required.
  • Strong data analysis skills.
  • Excellent organizational skills and attention to detail.
  • Ability to work independently and cross-functionally.

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.
  • Review in-process manufacturing documentation and resolve issues.
  • Lead process improvement initiatives and cross-functional collaboration.
  • Conduct workspace walkthroughs and calibrations to maintain compliance.
  • Perform training for new employees and support team development.

Skills

GMP experience
GDP knowledge
Fermentation (E. coli bioreactor)
Protein purification (TFF, chroma.,fil

Education

Bachelor's degree in related field
Master's degree in related field

Tools

Microsoft Office

Job description

Bio-Techne seeks an Advanced Research Associate to support the development and sustained manufacture of its diverse product portfolio. You will author, revise, and execute SOPs for reagents and consumables while facilitating controlled experiments to advance new products and implement process improvements.

In a fast-paced environment, you’ll ensure GDP compliance, perform data analyses, and collaborate with cross-functional teams to meet project objectives and maintain quality standards.

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