Job SummaryMedline is seeking a detail-oriented and collaborative Associate Support Engineer to join our Research, Development & Engineering (RD&E) team. In this role, you will be responsible for generating and maintaining high-quality technical documentation to support new product development within the Microtek-OEM division. You will work closely with engineers, project managers, and cross-functional partners to ensure that all documentation complies with regulatory and quality system requirements. This is a key role for ensuring the integrity and completeness of the design history file (DHF) for medical device products.
What's in It for You:
The opportunity to contribute to the development of innovative medical technologies that improve patient safety and care.
A chance to grow your career in a company that values precision, quality, and continuous improvement.
A collaborative and inclusive work environment that values diverse perspectives and ideas.
Job DescriptionResponsibilities: - Generate and maintain technical documentation for new product development, including risk management files, protocols, reports, and specifications.
- Apply Good Documentation Practices (GDP) to ensure accuracy, consistency, and compliance with regulatory standards.
- Collaborate with engineers, project managers, quality, and other cross-functional team members to gather and organize technical information.
- Support the creation and maintenance of design history files (DHF) in accordance with medical device regulations and internal quality systems.
- Assist in identifying opportunities to improve documentation processes and support project efficiency.
- Ensure all documentation aligns with applicable standards (e.g., ISO, FDA, GDP).
Minimum Qualification:Education - Bachelor's degree in an Engineering discipline.
Preferred Qualifications - Fluency in English, with strong written and verbal communication skills.
- Previous Internship Experience and/or experience in the medical device industry.
- Proven experience writing technical documentation such as protocols, reports, and specifications
- Working knowledge of Good Documentation Practices (GDP).
- Strong organizational skills and attention to detail
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:
$67,000.00 - $101,000.00 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.
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