Programming Associate Jobs in Miami, FL (NOW HIRING)

The Director, Engineering will be responsible for leading and managing a team of engineers, overseeing engineering for variety of teams, which may include any combination of manufacturing, sustaining, , process improvement, process validation, and calibration and preventive maintenance with responsibilities for supporting high-quality medical devices within the healthcare industry. This leader is accountable for sustaining engineering quality, leveraging engineering best practices, and creating process improvements aligned with operational efficiencies, quality standards, and manufacturing excellence aligned with the growth of the company and advancement of our portfolio. The role will be responsible for end-to-end aspects of engineering, aligned with day-to-day operations, defining the strategic direction of the engineering team to drive and sustain business growth in accordance with the company’s overall business goals.

• This position has responsibilities for developing and implementing technical strategies that drive innovation, optimize resources, and ensures the delivery of quality products to customers.
• Lead and manage engineering teams, ensuring that all members are working effectively and efficiently towards the goals set forth by the organization.
• Develop and drive validation and optimization of manufacturing processes
• Develop and execute equipment qualification, calibration and maintenance strategies
• Lead root-cause investigation for product and process failure; collaboration with Manufacturing and Quality team
• Provide stable and predictable manufacturing environment to manufacturing team through improving process, maintain equipment, and improve equipment usability
• Lead the development of technologies and equipment to enable improved product performance and efficiency in manufacturing.
• Lead and provide direct manufacturing engineering supporting product manufacturing across multiple portfolios.
• Provide technical input to the execution of the lifecycle management and supplier change notifications.
• Participate in portfolio development, management, and organizational oversight of the execution of operational cost down activities that deliver annual gross margin improvements to the product portfolios.

• Develop short-medium term plans to ensure engineering initiatives aligned with the companies’ long-term objectives and business strategies.
• Capable of providing and supporting lean methodology and other engineering best practices driving results in engineering for the future growth of the organization.
• Participate in manufacturing engineering activities for strategic planning, budgeting, expense management and project management review.
• Provide direct supervision, development, and performance planning leadership to leaders and direct report engineering associates, as assigned.
• Overall responsibilities for budget, timelines, and being fiscal responsibility, which includes driving cost and operational improvements in support of the company’s long-term strategic objectives.
• Collaborates closely with key stakeholders across the organization, to ensure that the engineering team is aligned with the needs of the business.
• Follow all established Environmental Health & Safety and Quality System policies, programs, rules and practices, including but not limited to product and patient safety, the health and safety of all associates as well as the environment and community at large.
• Prepare presentations and formally present to executive leadership.
• Lead special projects, as assigned
• Performs other duties, as assigned.

• Strong leadership ability with extensive knowledge of compliance to ensure adherence to engineering best practices and industry standards.
• Strong technical skills, project management, critical thinking skills and the ability to adhere to demands of on-time completion and within budget constraints.
• Extensive experience in the development of new and improvement of existing manufacturing processes for global Medical Devices or other highly regulated industries in accordance with global regulatory and quality standards and requirements.
• Proven experience with the use and upscaling automation and technology in a manufacturing environment,
• Proven track record of monitoring and maintaining compliance with engineering best practices and industry standards.
• Experience in the application of Design for Six Sigma (DFSS), Design for Manufacturability (DFM); Design for Assembly (DFA), Lean Six Sigma principles and tools and concurrent engineering principles.
• Demonstrated understanding of the cross-functional interactions needed for the development and manufacture of new products, preferably within FDA design control guidelines.
• Effective communication skills, both verbal and written; adept at communicating technical information to both technical and non-technical audiences.
• Ability to develop budgetary estimates and manage their execution.

• BS in Engineering or other related technical field with 10+ years in Medical Device, Pharmaceutical or other highly regulated industry in process development and/or manufacturing implementation/improvement.
• Advanced business MBA/Master's degree preferred
• Minimum of 7 years of proven overall experience leading engineering teams of +25 through development process for complex projects