R&D Intern/Co-Op — Biotech Research & Development

Solvita

Kettering (OH)

On-site

USD 21,000 - 30,000

Part time

6 days ago
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Job summary

Solvita is seeking a Research and Development Intern/Co-Op to assist with ongoing projects in allograft development and processing method improvements. You will collect data, analyze results, and help transition processes to production.

Under supervision, you will prepare reports and manuscripts for review, support pre-clinical work, and ensure compliance with regulatory standards. Strong communication and teamwork are essential.

Qualifications

  • Pursuing BS in engineering, chemistry, biochemistry, physiology or related science.
  • Ability to solve technical problems and analyze data.
  • Detail oriented with strong documentation and communication skills.
  • Proficient with Microsoft Office applications.

Responsibilities

  • Assist on R&D projects related to allograft development and processing method improvements.
  • Collect and analyze data using statistical tools.
  • Help transition new/improved processes into production.
  • Prepare reports and manuscripts for internal or external review.
  • Assist with surgical procedures in support of pre-clinical research as needed.
  • Ensure compliance with regulatory authorities and standard procedures.
  • Provide recommendations for work instructions, job aids and policies.
  • Perform other duties as assigned.

Skills

Technical problem solving
Data analysis
Documentation
Verbal & written communication
Cross-functional collaboration
Microsoft Office

Education

High School diploma

Tools

Microsoft Word
Microsoft Excel
Microsoft Access
Microsoft PowerPoint

Job description

Solvita is seeking a Research and Development Intern/Co-Op to assist with ongoing projects in allograft development and processing method improvements. You will collect data, analyze results, and help transition processes to production.

Under supervision, you will prepare reports and manuscripts for review, support pre-clinical work, and ensure compliance with regulatory standards. Strong communication and teamwork are essential.

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