Biomedical Engineering Director directs and coordinates biomedical equipment service operations that provide lifecycle management of biomedical clinical and research equipment including safety testing, repair, maintenance, and user support. Establishes standards and procedures for equipment maintenance, testing, calibration, documentation, and inventory processes. Being a Biomedical Engineering Director provides technical leadership and develops applicable training and resources for medical staff to ensure correct and safe operations of all equipment and devices. Works with vendors to maintain up-to-date information about new products and equipment upgrades. Additionally, Biomedical Engineering Director supports the equipment needs of all specialty areas including Radiology, Clinical Pathology, Cardiology, Respiratory Therapy, and others. Requires a bachelor's degree. Typically reports to a director or head of a unit/department. The Biomedical Engineering Director typically manages through subordinate managers and professionals in larger groups of moderate complexity. Provides input to strategic decisions that affect the functional area of responsibility. May give input into developing the budget. To be a Biomedical Engineering Director typically requires 3+ years of managerial experience. Capable of resolving escalated issues arising from operations and requiring coordination with other departments. (Copyright 2024 Salary.com)
Position Summary
The position will be based in North America, work closely with various operations departments, as well as the Quality, NPD, Brand Manager and Commercial departments within the company. The role will report to the Global Sr. Director of Engineering and will have three direct reports.
With the NA, Central America and the Caribbean rapid expansion, we need to bring into the organization a higher-ranking position to lead the Operations Model Infrastructure implementation.
The Engineering Director role will lead the Engineering and Packaging team to deliver:
1. Ownership of Monster specifications for our products and ensure that our Co packers and Suppliers adhere to the Monster Specifications in North America, Central America and the Caribbean.
2. These regions are growing ahead of demand, through plant qualification (Cans and Filling). In addition, our Kits models are expanding through our PREDATOR brand
3. Growing capability ahead of demand, through equipment installation / upgrade or packaging technology improvements.
4. Capital expenditure management, to ensure activities are delivered within approved cost.
5. Engineering and Packaging specialist knowledge to resolve and prevent issues from occurring.
6. The Director will be responsible for expansion of 30 million cases per year in North America alone, over the next 3 years.
7. Lead the implementation and launch of new sites for expansion in North America, Central America and Caribbean.
The role will directly lead plant start-ups for Production of Products, Equipment Installation and Packaging Qualification with direct communications with the original equipment manufacturer (OEM) packaging suppliers (Vendors) in North America, Central America and Caribbean regions including their Sales, Customer Service and manufacturing facilities.
The engineering team will determine Monster specifications, qualify packaging suppliers and document standards throughout North America to ensure all Cans, bottles, trays, Cap, Shrink and all other packaging is produced to Monster standards
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