• Supervise pre-service staff and workflows for scheduled services • Ensure patients are financially cleared in advance • Provide mentoring and developmental opportunities to staff • Oversee day-to-day operations of the Pre-Service team • Coordinate team activities for effective resource use • Develop expertise for Patient Access applications

• Lead cost estimation oversight across Utility-Scale Solar and BESS projects nationally. • Develop and progressively elaborate on capital expenditure estimates for project execution costs for Solar and BESS projects. • Perform detailed estimates of CapEx costs and prepare solicitation packages for 3rd parties. • Support Business Development team by executing estimating tasks and providing initial engineering/constructability reviews. • Conduct site visits as necessary to perform constructability diligence. • Develop and maintain internal and external project cost databases.

• Establish access management policies and standards and keep them current. • Plan and execute initiatives that improve access management capabilities. • Work with peers to automate onboarding, lifecycle and deprovisioning of privileged accounts. • Manage the entire service delivery process, from planning and implementing service strategies to monitoring and reporting on service performance. • Establish policies, procedures, and standards through periodic review and change management. • Support regulatory requirements and perform audits.

Symmetrio is recruiting for our client for a Regulatory Affairs Manager to lead U.S. regulatory strategy and submissions for innovative healthcare software products. This role will focus on FDA 510(k) submissions and regulatory pathways for Software as a Medical Device (SaMD) within a global, multinational environment.    Key Responsibilities  - Lead preparation and submission of FDA 510(k) filings for healthcare software and digital health products  - Develop and execute regulatory strategies supporting product development and commercialization  - Collaborate with product development, quality, clinical, and engineering teams to ensure regulatory compliance  - Interpret FDA guidance related to medical device software and digital health technologies  - Partner with global regulatory teams to support international regulatory initiatives