R&D Lab Associate — Biocompatibility & Testing

Medline Industries, LP; Mundelein (IL); On-site; USD 62,000 - 93,000; Full time

Benefits offered by this job

health insurance

life and disability

401(k) contributions

paid time off

Employee Assistance Program

Employee Resource Groups

Employee Service Corp.

Job summary

Medline Industries, LP in Mundelein, IL is seeking a chemistry/biology-oriented professional to support the development of new products and technologies within the R&D group. The role will focus on performance testing and related regulatory activities, including biocompatibility assessments and risk reviews.

You will plan and execute testing, author protocols and reports, compile data, and ensure compliance with regulatory requirements related to product development and safety.

Qualifications

• Education: Bachelor of Science in Chemistry, Biology or related field.
• Certification / Licensure: None
• Work Experience: None
• Knowledge / Skills / Abilities: Position may require travel up to 10% of the time for business purposes (domestic and international).

Responsibilities

• Plan and execute or otherwise facilitate testing required in support of a product claim.
• Author test protocols and reports.
• Compile and review test results relative to meet product regulatory testing requirements.
• Compile data summaries in support of product claims.
• Ensure compliance in all research, data collection, and reporting activities for regulatory requirements related to biocompatibility and R&D product development, design, stability, safety and efficacy.

Skills

Travel up to 10%

Education

Bachelor of Science in Chemistry, Biology or related field

Job description

Medline Industries, LP in Mundelein, IL is seeking a chemistry/biology-oriented professional to support the development of new products and technologies within the R&D group. The role will focus on performance testing and related regulatory activities, including biocompatibility assessments and risk reviews.

You will plan and execute testing, author protocols and reports, compile data, and ensure compliance with regulatory requirements related to product development and safety.