Senior Manufacturing Engineer

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 Job Function : Supply Chain Engineering Job Sub Function : Manufacturing Engineering Job Category : Scientific / Technology All Job Posting Locations : Anasco, Puerto Rico, United States of America Job Description : Key responsibilities

• Leads and executes projects and / or programs of moderate to high level of complexity ensuring safety, regulatory compliance, company standards, operation requirements and business needs.
• Drive the optimization of process output and throughput, equipment utilization, equipment downtime, waste reduction / yield improvements, budget management, standard cost, and capital investment management in a creative manner.
• Provides technical support to peers and production areas in evaluating process deficiencies, process changes, modifications, and equipment failure. Defines, analyzes, reviews, and evaluates problems for prompt solutions.
• Sets the engineering standard and direction for the group and is recognized as the source for mentorship in a field.
• Financial management and scheduling – Prepare project estimates for design, equipment, installation, labor, materials, and other related costs. Prepare project forecast, schedules, and tracks costs.
• Challenges the “status quo” on a routine basis and develops new ideas within incoming processes.
• Drive phases of work with different site functions and with other divisions.
• Technical support for Non-conformance issues in the manufacturing area generating investigation reports and corrective action identification (Coordinates and participates on Multi-functional Investigation).
• Supports manufacturing in the day-to-day troubleshooting of equipment’s to ensure increase production outputs and increase operation team capabilities.
• Follows Standard Operating Procedures (SOP), Good Manufacturing Practices (GMPs), Company Policies and Federal, State and Local Government Regulations.
• Revise and maintain engineering, equipment’s, and process procedure. Qualifications
• Bachelor’s Degree in Engineering
• Minimum of 4 years of experience is required in a maintenance manufacturing environment, R&D or Process Development.
• Experience working at medical device industry or pharmaceutical, preferred.
• Demonstrated experience in Project Management, preferred.
• Knowledge in Control Systems, Automation and familiar with Vision Systems, preferred.
• Experience in Computer Systems Validation, preferred.
• Proven experience with validation cycle (FAT, IQ, OQ and PQ), preferred.
• Proven experience with Lean, process optimization, preferred.