Senior Engineer, MFG ENGR

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 ;br>
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:

Johnson & Johnson is recruiting for a Senior Process Engineer located in its manufacturing site at Aasco, Puerto Rico.

About MedTech

Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments.

Your unique talents will help patients on their journey to wellness. Learn more at ;br>
Under the direction of the Engineering Manager, handles most aspects of a project or initiatives. Role is responsible for problem identification, reporting, root cause analysis, project management, financial analysis, efficiency or productivity improvement, reporting, and problem resolution. Role interfaces directly with other departments, sites, and corporate functional groups to drive and/or support critical business goals/objectives within GMP/ISO compliance. Lead/Support continuous improvement activities to ensure business key performance indicators are met. Lead groups of Engineers or Technicians on projects or special assignments. Creates and presents CAR for the Projects responsible.

Key responsibilities

• Leads and delivers 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 problem solving of equipments 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.
• Support the GMP audits as subject matter guide for product and processes.
• Coordinates communications and interfaces within end users and machine manufacturers or suppliers.
• Lead or participates in projects involving other departments and activities.
• Evaluates process trends (Ex. Yield, OEE) to drive improvements of business results.
• Daily monitoring and support to manufacturing lines
• Provide training on process and validation requirements to operators and engineers
• Writes, develops, and implement validation strategies.
• Works independently. Plans and develops own methods. Takes actions in the absence of specific instructions. Develops and presents new or improved methods. Solves manufacturing problems in a timely manner.
• Stay in sync with all environmental, safety and occupational health policies

Qualifications

• Bachelor's Degree in Engineering
• Proven experience of 4 years 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.
• Performed Design Reviews with vendors on automated equipment.

Johnson & Johnson is an 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, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, please contact us via or contact AskGS to be directed to your accommodation resource.