CAREGIVERS AND MED TECHS OPEN HOUSE
WALK INS WELCOME - ON SITE INTERVIEWS
WILLOWBROOK HILLS is hosting an Open Interview Event for Caregivers and Med Techs on Wednesday, November 11th from 10am to 1:30pm at our location in Auburn Hills, MI (3151 E Walton Blvd). No appointments necessary, walk-ins welcome, interviews on-site. This is a great opportunity to meet our team, learn more about the role, and explore employment opportunities with Willowbrook Hills. Whether you are an experienced caregiver that is looking for a fresh start or interested in becoming a new caregiver, come meet us this Wednesday, November 11th, and see why we are Oakland County's premiere assisted living and memory care community!
Senior Programmes Officer responsible for coordinating and delivering in-person and virtual work experience and employer engagement for the Sutton Trust’s Pathways to Banking & Finance and Access Apprenticeships programmes.
Compensation
Salary: £36,200
Responsibilities
Coordinating the effective delivery of high-quality in-person and virtual work experience and employer engagement
Liaising with employers, universities and Sutton Trust colleagues to match students with relevant activities
Following up with students regarding absences or non-attendance at placements
Promoting volunteering opportunities at events
Managing and stewarding placement providers and funders
Lead global regulatory strategy for novel farm and companion animal products, negotiating with agencies such as FDA CVM and EMA.
Locations (2)
Indianapolis, Indiana, United States
United States
Compensation
Elanco currently anticipates that the base salary for this position could range from $118,000 to $197,000 depending partly on the successful candidate's qualifications, including education and experience.
Responsibilities
Guide the design and development of the global regulatory strategy for development projects
Serve as the dedicated regulatory subject matter expert on development teams
Act as the primary point of contact for and lead direct engagements with regulatory agencies
Partner with R&D to develop and implement clinical trial submission plans
Collaborate with internal stakeholders to provide technical leadership on Quality, Safety, and Efficacy sections