UL, LLC Microsite

. Within the framework of our highly regulated Medical Regulatory Programs you will:

• Supervisor Responsibilities of a local team of Auditor/Lead Auditors to ensure business needs as well as individual goals are met within expected timeframes (e.g. projects delivery, training plans development and execution; individual professional development);

• Support contract review / agenda setting for quality management system audits.

• Support regular quality system and technical audits, including CE unannounced audits.

• Provide timely Audit Reports and customer Corrective and Preventive Action analysis and responses.

• Subject to training and qualification milestones, perform key Quality Management System audit activities to support safe products to market.

• Support Competent Authority activities on as needed basis e.g. Competent Authority audits of UL.

• Participate in the development of UL requirements and assessment methods. Integrate continuous improvement concepts into all aspects of the job.

• Provide guidance and support to customers as required. Participate in client training and customer forums.

• Performs other duties as directed.

Medical Devices are some of the most regulated products in the world. In this role, you will be a part of the UL Medical Regulatory Team. Working as the SME expert with limited supervision, you will independently assist and support processing of manufacturer submissions to the ISO13485 and MDSAP programs, UKCA Medical Device Regulation 2002 and the CE Medical Device Regulation 2017/745. Within the framework of our highly regulated Medical Regulatory Programs you will:

• Supervisor Responsibilities of a local team of Auditor/Lead Auditors to ensure business needs as well as individual goals are met within expected timeframes (e.g. projects delivery, training plans development and execution; individual professional development);

• Support contract review / agenda setting for quality management system audits.

• Support regular quality system and technical audits, including CE unannounced audits.

• Provide timely Audit Reports and customer Corrective and Preventive Action analysis and responses.

• Subject to training and qualification milestones, perform key Quality Management System audit activities to support safe products to market.

• Support Competent Authority activities on as needed basis e.g. Competent Authority audits of UL.

• Participate in the development of UL requirements and assessment methods. Integrate continuous improvement concepts into all aspects of the job.

• Provide guidance and support to customers as required. Participate in client training and customer forums.

• Performs other duties as directed.

— successful completion of a university or a technical college degree or equivalent qualification in relevant studies, such as medicine, pharmacy, engineering or other relevant sciences;

— four years' professional experience in the field of healthcare products or related activities, such as in manufacturing, auditing or research, of which two years shall be in the area of quality management;

-- For Product Review applications, the following additional requirements are a must:

— four years' professional experience in the field of healthcare products or related activities, such as in manufacturing, auditing or research, of which two years shall be in the design, manufacture, testing or use of the device or technology to be assessed or related to the scientific aspects to be assessed;

— knowledge of device legislation, including the general safety and performance requirements set out in MDR Annex I;

— appropriate knowledge and experience of clinical evaluation;

— appropriate knowledge of the devices which they are assessing;

— appropriate knowledge and experience of the conformity assessment procedures laid down in MDR Annexes IX to XI, in particular of the aspects of those procedures for which they are responsible, and adequate authorisation for carrying out those assessments;

— appropriate knowledge of devices legislation as well as related harmonised standards, i CS and guidance documents;

— appropriate knowledge and experience of risk management and related device standards and guidance documents;

— appropriate knowledge of quality management systems and related standards and guidance documents;

— appropriate knowledge and experience of the conformity assessment procedures in the listed programs (MDSAP, ISO13485, MDD/MDR, etc), in particular of the aspects of those procedures for which they are responsible, and adequate authorisation for carrying out those audits;

— training in auditing techniques enabling them to challenge quality management systems;

— the ability to draw up records and reports demonstrating that the relevant conformity assessment activities have been appropriately carried out;

• Valid CNCA/CCAA auditor Registrations

A global leader in applied safety science, UL Solutions transforms safety, security, and sustainability challenges into opportunities for customers in more than 100 countries. UL Solutions delivers testing, inspection and certification services, together with software products and advisory offerings, that support our customers’ product innovation and business growth.

The UL Certification Marks serve as a recognized symbol of trust in our customers’ products and reflect an unwavering commitment to advancing our safety mission.

We help our customers innovate, launch new products and services, navigate global markets and complex supply chains, and grow sustainably and responsibly into the future.

From the adoption of electrification to the enablement of 5G and new mobility, we collectively look toward new frontiers, working for a safer world.​ Our science is your advantage.

Mission: Working for a safer world

UL LLC has been and will continue to be an equal opportunity employer. To assure full implementation of this equal employment policy, we will take steps to assure that:

Persons are recruited, hired, assigned and promoted without regard to race, color, age, sex or gender, sexual orientation, gender identity, gender expression, transgender status, religion, creed, national origin, ethnicity, citizenship, ancestry, disability, genetic information, military or veteran status, pregnancy, marital or familial status, or any other protected category under applicable law.