• Provide comprehensive clinical services for children and teens with ADHD and their families, with a focus on diagnostic and medication management. • Collaborate with a multidisciplinary team that includes MD’s, nurse practitioners, psychologists and other clinicians to provide excellent care. • Complete administrative work and clinical documentation in a timely and accurate manner. • Contribute to implementation, evaluation and program development iteration to ensure optimal delivery of care. • This is a clinical position, but there may be opportunities to expand and grow into program development, and other leadership activities, depending on employee interest and company needs.

• Provide high-quality telemedicine care • Engage with patients through video-audio appointments • Collaborate with patient care advocates for follow-up • Stay informed on patient coverage and insurance plans • Utilize technology effectively in care delivery

• Deliver precise, evidence-based strength training • Coach members clearly and confidently • Build strong relationships that lead to retention and referrals • Lead Introductory Workouts that inspire commitment • Maintain excellent attendance and help members achieve real results • Improve continuously — Kaizen is part of our DNA

• In conjunction with Global Head of Certification and compliance and QA & RA Manager, liase with regulatory authorities and other certification bodies on all technical/regulatory questions to ensure the integrity and compliance of all in vitro diagnostics certification processes and decisions. • Provide technical lead and expertise to the global Medical Devices network, including the sales and commercial teams, relating to in vitro diagnostic medical device certification, as well as the respective medical device scheme managers (ISO13485, MDSAP, UKCA). • Lead the team of IVDR product assessors and IVDR IHC. • Support the Training and Competency Manage and CV reviewer in conformity assessment and CV review. • Develop, update and maintain appropriate training packages for IVDR Product Assessors within the in vitro diagnostic medical device conformity assessment process in collaboration with Training and competences manager. • Manage the in vitro diagnostic medical device training process for both existing and new IVDR Product Assessors and IVDR IHC within the in vitro diagnostic medical device conformity assessment process. • Provide technical advice to support all stages of the in vitro diagnostic medical device conformity assessment process in collaboration with IVDR FR & CDM Team Leader. • Develop, maintain and implement QMS documentation related to in vitro diagnostic medical devices conformity assessment process of SGS NB 1639 with QA & RA Manager, aligned with best practices (e.g. MDCG guidance documents) and applicable regulatory and accreditation requirements. • Establish competence criteria for Technical Experts. • Approval of mirror reviews for IVDR Product Assessors related to IVDR qualification and requalification requirements. • Manage the development and implementation, including approval process for and IVDR Product Assessors and IVDR IHC (new personnel & for on-going monitoring and re-approval of personnel). • Contribute to the day-to-day management and business development of the in vitro diagnostic medical devices activities to achieve defined operational and financial targets and maintain both technical and regulatory compliance.