Overview Nationwide Search - Selected candidate can be located anywhere in the United States. We are seeking experienced Director of Healthcare Facilities Management or similar for our Life Safety Code surveyor opportunities. Life Safety Code Surveyors review assigned functions in Environment of Care throughout the United States. Provides general evaluation services, education, and consultation consistent with applicable Joint Commission standards, policies, and protocols. Determines the degree of compliance with applicable standards, specifically NFPA101 Life Safety Code. Qualifications Education: - Bachelor’s degree in related field required. - College degree must be from accredited institutions of higher learning. Certification/Licensure/Registration: - Current certification/licensure/registration in a field related to plant, technology, and/or safety management preferred [i.e., Certified Healthcare Facility Manager (CHFM), Certified Healthcare Safety Professional (CHSP), Healthcare Environmental Manager (HEM), Certified Industrial Hygienist (CIH), Certified Safety Professional (CSP), Professional Engineer (PE)] - Certification requirement: You must hold a CPHQ certification (Certified Professional in Healthcare Quality) through National Association for Healthcare Quality (NAHQ) at time of hire or attain within by December 31, 2028. General Knowledge and Experience: - - Five years required in a management position in engineering, facilities management, hazardous materials and waste management, emergency preparedness, biomedical equipment, and/or utility systems or as experience as the organization’s Safety Officer. - Eight years of hospital experience in facilities management preferred; - Knowledge of Joint Commission Physical Environment standards, including the Life Safety Code (NFPA101), the Health Care Facilities Code (NFPA 99) and other relevant NFPA standards and direct involvement with a minimum of two Joint Commission surveys. - Specialized knowledge of building systems, utility systems, and fire protection systems. Must be able to lift 25 lbs., climb stairs and ladders. All positions require 100% nationwide travel. Please review the following employment statuses. We offer full-time and part-time opportunities. *Candidates interested in part time positions must be available to work two weeks (.48 FTE) or three weeks (.7 FTE) per month, and must provide three or four weeks of availability for scheduling purposes. Physical Abilities: - Must be able to observe, in real time and without slowing or otherwise interrupting the progress of, all applicable types of ongoing health care treatment (e.g., including emergency treatment, treatment during weather and other extreme situations, etc.). - Standing for long periods of time, walking lengthy distances, lifting, climbing, stooping, pulling, and pushing in order to adequately inspect and observe all medical facilities, equipment and procedures, such as emergency exit procedures, remote storage facilities, any areas where cleanliness may affect the possibility of infection, medical equipment, etc., including the following activities: - walking up and down stairways (e.g., to test escape routes, assess safety of emergency exits, regulatory compliance, etc.); - removing obstructed covers or impediments to equipment or other mechanical areas; - examining small and often dirty printed labels and print on equipment; - Must be able to engage in extensive travel as set forth above, including driving a car to remote locations, flying on small airplanes and into small airports, traveling in all types of weather conditions, etc. We are currently hiring for our next orientation class to take place on May 4, 2026 and June 8, 2026 This job description is intended to describe the general nature and level of work performed by an employee assigned to this position. The description is not an exhaustive list of all duties, responsibilities, knowledge, skills and abilities, and working conditions associated with this position. All requirements are subject to possible modification and reasonable accommodation for qualified individuals with disabilities. Nothing in this job description alters the at-will nature of employment at the Joint Commission. The Joint Commission offers comprehensive benefits package. For a complete overview of our benefits package, please visit our Joint Commission Career Page #LI-REMOTE Min USD $112,000.00/year Max USD $112,000.00/year

• Develop and apply deep and extended technical expertise of current regulatory, industry and emerging trends in compliance. • Develop, implement, and maintain a robust compliance framework that aligns with all applicable laws and regulations in Singapore. • Ensure timely and accurate submission of all regulatory reports to the relevant authorities (MAS, ACRA, IRAS). • Work closely with Legal, Finance, and People (HR) teams to ensure that all relevant regulations are identified and addressed.

Role Description This role is an exciting opportunity to join our dynamic and ambitious Regulatory Affairs team. The role is part-time and involves performing as Local Regulatory Affairs Expert providing consultancy services related to marketing authorizations and supporting regulatory activities for pharmaceutical products in Malta. Furthermore, candidates must be able and willing to legally work as a Freelancer and be based and have experience working in Malta. - Provides local regulatory consultancy and expert advice related to Marketing Authorization (MA) applications and amendments - Supports preparation, submission, and follow-up of MA applications and variations with local Health Authorities - Manages ongoing regulatory activities for authorized products to ensure continuous compliance with national requirements - Provides support for Decentralized Procedure (DCP) lifecycle management and national phase activities - Reviews and ensures alignment of product information, labelling, and packaging with local regulatory standards - Monitors national regulatory changes and communicates relevant updates to stakeholders - Provides ad-hoc regulatory support and guidance as needed - Collaborates closely with global and regional Regulatory Affairs teams to ensure consistency and compliance Qualifications - University Degree in Life Sciences, Pharmacy, or a related field - Minimum of 2 years of relevant experience in Regulatory Affairs, preferably within a global or regional pharmaceutical environment - Previous experience in marketing authorization applications, variations, and lifecycle management in Malta is highly valued Requirements - Strong organizational and analytical skills with a high level of attention to detail - Proven ability to work both independently and collaboratively in a dynamic, multinational context - A proactive, client-oriented mindset and the ability to manage multiple priorities efficiently - Proficiency in MS Windows and MS Office applications - Familiarity with national and EU regulatory systems (e.g., CESP, eCTD, DCP) is considered an asset - Excellent command of English (written and spoken) and local language - Knowledge of additional European languages is considered an advantage - Self-motivated, adaptable, and an effective communicator - A strong team player with a genuine interest in contributing to Excelya’s mission and supporting high-quality regulatory outcomes Benefits At Excelya, taking audacious steps is encouraged, so we’re looking for individuals who are ready to grow with us and share our values of Audacity, Care, and Energy. - We combine passion for science with enthusiasm for teamwork to redefine excellence in healthcare - We are a young, ambitious health company representing 900 Excelyates, driven to become Europe’s leading mid-size CRO with the best employee experience - Our one-stop provider service model offering full-service, functional service provider, and consulting enables you to evolve through diverse projects - Working alongside preeminent experts, you will help improve scientific, operational, and human knowledge to enhance the patient's journey - Excelling with care means benefiting from an environment that values your natural talents, pushes boundaries with audacity, and nurtures your potential

• Own our security and compliance documentation accurate and up to date, such as policies, procedures, and support documentation across our information security and compliance programs. • Support our commercial teams in complex information security and compliance negotiations, while making sure we respond accurately and within given timescales. • Take ownership of maintaining our current ISO 27001 compliance and certification through continuous improvement activities, as well as supporting preparation for internal and external audits. • Own our internal Data Protection compliance program and make sure we comply with various regulations globally including UK GDPR, EU GDPR, and CCPA. • Gain experience in the implementation and ownership of additional compliance based projects as we increase the international regulation and standards we comply with. • Help us work efficiently by identifying common deal blockers and standardising documentation and processes.