E980 | Sr Engineering Manager Digital Surgery

hace 3 semanas

Salamanca, España Importante Grupo A tiempo completo

Johnson & Johnson MedTech is recruiting for a Sr Engineering Manager Digital Surgery located in Palm Beach Gardens, FL
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
Provides leadership and direction to the Engineering staff for the Orthopaedics Digital Surgery platform, including the Palm Beach Gardens and Oberdorf manufacturing sites to ensure that production goals related to quality, safety, delivery, manufacturability and cost are consistently met.
Areas of focus include Team Leadership, Manufacturing Engineering, Support External Manufacturing, Technology, New Product Introduction, Life Cycle and other special projects.
Oversees budgets, staffing needs, production, and employee performance on a regular basis.
Works with all levels of management and production employees to continuously improve productivity and efficiency of manufacturing and production operations; verifying that resources vital to meet those goals are available and qualified.
Are you interested in making a difference in a thriving diverse company culture that celebrates the uniqueness of our employees and is committed to inclusion?
Apply today
Key Responsibilities:Promote a quality-focused culture within the Site MAM Team, ensuring alignment to cGMP's and Quality Systems as defined in the Quality Manual.Deliver Continuous Improvement Objectives and Manufacturing Targets (Quality, Productivity, Service Growth and Cost) in partnership with BEX, Operations and Site Quality Teams.Leadership of talent development and organizational people strategy.Support the continuous development of Global engineering excellence through the effective use of talent in key assignments in the Engineering Excellence program.Prioritization of key initiatives in alignment with short and long-term strategies based on needs of customers and overall business.Execution of appropriate standardization practices and processes (e.g.
Validation, Compliance, EH&S, Facility, Digital, Automation, Reliability).Act as a link between LCM, New Product, E2E Engineering Delivery, Direct Materials and Manufacturing Innovation functions to deliver to meet short, medium, and long-term business goals on the Manufacturing Site.Implement common technical standards, software systems and capital equipment in respect of Asset Replacement and Risk Reduction Activities on the Manufacturing Site.Integrate New Technologies to the Manufacturing Site in a consistent and reliable manner to ensure stable Product Delivery in the areas of Process Engineering, Maintenance, Reliability and Process Improvement (3D Printing, HA Coating Technologies, etc).Build and implement a pipeline of Technical Projects to meet or exceed business targets in Quality, Service, Growth and Value – in partnership with the BEX and Plant Operational Teams, per DPM Metrics on the Manufacturing Site.Implement and Integrate Digital & Automation Strategies on the Manufacturing Site in line with Manufacturing best standards (with particular focus on Cybersecurity); anticipate and influence technology requirements to meet Manufacturing Site Needs.Diligently participate in our compliance program-related activities as denoted by your supervisor or our Chief Compliance Officer.Responsible for communicating business-related issues or opportunities to next management level.For those who supervise or manage a staff, responsible for ensuring that subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicable.Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures.Performs other duties assigned as needed.
Qualifications:Education: Minimum of a Bachelor's degree in Engineering, Science or a related subject area is required; PhD or MBA degree/Studies is preferred.Experience and Skills:Minimum 10 years of Engineering, Operations, Product Development or Quality Management experience in medical devices or regulated industry.Minimum of 5+ years of Senior Managerial Experience.Working knowledge of process development and validation, including design of experiments, statistical analysis, and project management.Organizational change, project management, and the ability to work effectively and drive alignment in a global environment through strong communication and empowerment.Outstanding leadership capability – demonstrated ability to motivate and inspire a global engineering team to drive significantly increased performance through technical innovation, business process innovation and change.Previous portfolio management expertise developing and implementing processes for new products on a global scale.Strong strategic vision and a willingness to be hands-on in all aspects of global manufacturing and supply chain operations, as appropriate.Ability to influence at different levels of an organization & a strong ability to communicate and collaborate with key partners.Excellent communication skills (written and oral).Problem-solving skills - to assist in maintaining project progress and on design issues.Excellent planning and organizing skills.Managing risk and crisis, including investigation, escalation, prioritization and resolution of systems and support issues and developing and managing responses.Demonstrate ability to solve complex technical problems involving technologies like those used in Digital Surgery products and deal with a variety of concurrent projects and tasks.Ability to read and interpret documents such as engineering specifications and drawings, safety rules, and operating procedures.Proficient in MS Office and engineering analysis tools.Preferred:Knowledge of sterile packaging and label is helpful.J&J certifications or alternatives preferable – PMP, FPX, MAMC, DRIVE.Process excellence qualifications in tool sets such as LEAN & Six Sigma, with a proven track record of deploying these tools to improve operational performance.Other: Fluent English is required.
Travel up to 10% (international).Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com.
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