Job Summary

Lead advanced, technical sterilization support for sterilization related projects among various Medline product divisions, sterilization facilities, and contract laboratories to maintain compliance to regulations and industry standards (e.g. 21 CFR Part 820, ISO11135, ISO11137, ISO13485 etc.). Apply engineering, microbiology and chemistry principles to develop, support and troubleshoot sterilization processes and challenges across multiple modalities.

Job Description

Responsibilities:

Provide expert technical expertise for sterilization related projects for all modalities used by the company including ethylene oxide, radiation, and steam. - Interact directly with FDA, notified bodies, and customers.
Develop responses to sterilization related requests and audit findings.
Provide technical support as needed during audits of Medline facilities, sterile vendors, sterilization facilities, and contract laboratories to make sure they comply with regulatory requirements.
Participate in technical committees such as AAMI sterilization standards development.
Active participation includes reviewing proposed standards and submitting comments as well as attending periodic meetings.
Monitor sterilization industry practices against internal processes and create or update procedures to maintain industry and regulatory compliance.
Develop sterilization training materials.
Conduct training for the sterilization department, other quality team members, and divisional personnel.
Develop and review statistical analysis data and make recommendations for improvement as well as establish implementation plans.
Meet with divisional personnel to provide technical assistance and make decisions related to ethylene oxide, steam, and radiation sterilization processes. Facilitate completion of sterilization activities on time as committed. Participate and support projects for international sterilization teams.
Onsite participation may be required.

Qualifications:

Bachelor's Degree with a scientific or engineering background.
Certification / Licensure - CISS (Certified Industrial Sterilization Specialist).
At least 4 years of direct experience working in the industrial sterilization of healthcare products. This must include EO cycle development and validation, radiation dose setting, and moist heat experience.
Experience supporting sterilization topics to regulators (e.g. FDA, ISO NB) during audits and inspections.
Strong understanding of ISO 11135, ISO 11137, and ISO 17665.
Strong understanding of microbiology principles related to terminal sterilization.
Strong understanding of chemistry principles related to EO/ECH residuals. Ability to work safely in environments where hazardous chemicals may be encountered under corporate safety rules and requirements.
Position requires travel up to 20% of the time for business purposes (within state and out-of-state).

Preferred Qualifications:

Member of AAMI sterilization working groups/committees.

Benefits - Medline is committed to offering competitive benefits and a variety of choices to best meet the needs of you and your family. For employees scheduled to work at least 30 hours per week, this includes health and well-being, financial fitness, career development, paid time off and more. Employees scheduled to work less than 30 hours per week can participate in the 401(k) plan, access the Employee Assistance Program (EAP), Employee Resource Groups (ERG) and Medline Service Corps. For a more comprehensive list of our benefits, please click here.

Every day, we're focused on building a more diverse and inclusive company, one that recognizes, values and respects the differences we all bring to the workplace. From doing what's right to delivering business results, together, we're better. Explore our Diversity, Equity and Inclusion page here.

Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.