R&D Specialist

Medline Industries

Full-Time

R&D Specialist

Medline Industries

Full-Time

Nov 04, 2025

Healthcare Services

Job Description

Job Summary

Responsible for contributing to the development of new products and technologies within the R&D group. The role will be a subject matter expert in a specific support area and will facilitate project needs related to that knowledge. Areas of focus may include performance testing, chemical characterization, stability testing, biocompatibility, toxicological assessments, risk assessments, etc.

Job Description

Responsibilities:

Plan and execute or otherwise facilitate testing required in support of a product claim.
Author and review test protocols and reports.
Track, compile, and review all results needed in support of product requirements and regulatory submissions such as 510k’s, CE technical files, and ANDA/NDAs. Compile technical justifications and data summaries in support of product claims. Identify and support the development of product requirements, performance attributes, and quality specifications. Coordinate verification and validation activities.
Ensure compliance of all data collection activities with applicable regulatory requirements.
Participate in the support of internal and external audits.
Compile risk assessments, identify gaps, and propose solutions.
Lead process improvement, CAPA, OOS investigations, and data trending activities.
Represent Medline on various ASTM/AAM/ISO technical committees and contribute to the development of new test standards.

Qualifications:

Bachelor’s degree in Chemistry, Biology or related science field.
A least 2 years of experience in a medical device or pharmaceutical related field.
Knowledge of FDA requirements and experience with FDA interactions as part of the 510k/ANDA/NDA approval processes.
Knowledge of CE technical files. - Experience with risk assessment and root cause analysis.
Experience solving practical problems and dealing with a variety of concrete variables in situations where only limited standardization exists.
Experience communicating with internal and external business partners and cross functional teams with various audiences.
Self-starter, independent worker, detail oriented with critical thinking and excellent organizational, analytical and problem solving skills.
Position may require travel up to 10% of the time for business purposes (domestic and international).

Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education & training, and tremendous potential with a growing worldwide organization.

The anticipated salary range for this position:

$73,840.00 - $107,120.00 Annual

The actual salary will vary based on applicant’s location, education, experience, skills, and abilities. This role is bonus and/or incentive eligible. Medline will not pay less than the applicable minimum wage or salary threshold.

Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For a more comprehensive list of our benefits please click here. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp.

We’re dedicated to creating a Medline where everyone feels they belong and can grow their career. We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best. Explore our Belonging page here.

Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws.

Job Summary

Job Description

Responsibilities:

Plan and execute or otherwise facilitate testing required in support of a product claim.
Author and review test protocols and reports.
Track, compile, and review all results needed in support of product requirements and regulatory submissions such as 510k’s, CE technical files, and ANDA/NDAs. Compile technical justifications and data summaries in support of product claims. Identify and support the development of product requirements, performance attributes, and quality specifications. Coordinate verification and validation activities.
Ensure compliance of all data collection activities with applicable regulatory requirements.
Participate in the support of internal and external audits.
Compile risk assessments, identify gaps, and propose solutions.
Lead process improvement, CAPA, OOS investigations, and data trending activities.
Represent Medline on various ASTM/AAM/ISO technical committees and contribute to the development of new test standards.

Qualifications:

Bachelor’s degree in Chemistry, Biology or related science field.
A least 2 years of experience in a medical device or pharmaceutical related field.
Knowledge of FDA requirements and experience with FDA interactions as part of the 510k/ANDA/NDA approval processes.
Knowledge of CE technical files. - Experience with risk assessment and root cause analysis.
Experience solving practical problems and dealing with a variety of concrete variables in situations where only limited standardization exists.
Experience communicating with internal and external business partners and cross functional teams with various audiences.
Self-starter, independent worker, detail oriented with critical thinking and excellent organizational, analytical and problem solving skills.
Position may require travel up to 10% of the time for business purposes (domestic and international).

Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education & training, and tremendous potential with a growing worldwide organization.

The anticipated salary range for this position:

$73,840.00 - $107,120.00 Annual

About Medline Industries

Medline is the largest provider of medical-surgical products and supply chain solutions serving all points of care. Through its unique offering of world-class products, supply chain resilience and clinical practice expertise, Medline delivers improved clinical, financial and operational outcomes. Headquartered in Northfield, Illinois, the company employs 43,000 people worldwide and operates in over 100 countries and territories.

It has always been Medline's intention and purpose to create a great place to work for everyone. We believe tapping into the richness of our employees' diversity allows us to find innovative solutions for our customers, who themselves represent a diverse group both in the U.S. and around the world. The Belonging and Engagement team at Medline is dedicated to fostering an inclusive and supportive workplace culture. We focus on creating opportunities for employees to feel seen, supported, and connected through initiatives like Employee Resource Groups (ERGs), cultural awareness events, new hire engagement, and leadership training.

Every hour of every day, healthcare professionals rely on Medline to help them do their job. Our agile and resilient global team is determined to get our customers exactly what they need, at the right time, every time. If you're a self-starter, eager to grow your career within a high-performing environment, this is the place for you. Together, we make healthcare run better.

For more on all things Belonging at Medline Industries, check out our home page here.

R&D Specialist

R&D Specialist

Job Description

Responsibilities:

Plan and execute or otherwise facilitate testing required in support of a product claim.

Author and review test protocols and reports.

Ensure compliance of all data collection activities with applicable regulatory requirements.

Participate in the support of internal and external audits.

Compile risk assessments, identify gaps, and propose solutions.

Lead process improvement, CAPA, OOS investigations, and data trending activities.

Represent Medline on various ASTM/AAM/ISO technical committees and contribute to the development of new test standards.

Qualifications:

Bachelor’s degree in Chemistry, Biology or related science field.

A least 2 years of experience in a medical device or pharmaceutical related field.

Knowledge of FDA requirements and experience with FDA interactions as part of the 510k/ANDA/NDA approval processes.

Knowledge of CE technical files. - Experience with risk assessment and root cause analysis.

Experience solving practical problems and dealing with a variety of concrete variables in situations where only limited standardization exists.

Experience communicating with internal and external business partners and cross functional teams with various audiences.

Self-starter, independent worker, detail oriented with critical thinking and excellent organizational, analytical and problem solving skills.

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 and review test protocols and reports.

Ensure compliance of all data collection activities with applicable regulatory requirements.

Participate in the support of internal and external audits.

Compile risk assessments, identify gaps, and propose solutions.

Lead process improvement, CAPA, OOS investigations, and data trending activities.

Represent Medline on various ASTM/AAM/ISO technical committees and contribute to the development of new test standards.

Qualifications:

Bachelor’s degree in Chemistry, Biology or related science field.

A least 2 years of experience in a medical device or pharmaceutical related field.

Knowledge of FDA requirements and experience with FDA interactions as part of the 510k/ANDA/NDA approval processes.

Knowledge of CE technical files. - Experience with risk assessment and root cause analysis.

Experience solving practical problems and dealing with a variety of concrete variables in situations where only limited standardization exists.

Experience communicating with internal and external business partners and cross functional teams with various audiences.

Self-starter, independent worker, detail oriented with critical thinking and excellent organizational, analytical and problem solving skills.

Position may require travel up to 10% of the time for business purposes (domestic and international).

About Medline Industries

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