At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are 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 more at .
As guided by Our Credo Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson we respect the diversity and dignity of our employees and recognize their merit.
Job Function:
Supply Chain EngineeringJob Sub Function:
Manufacturing EngineeringJob Category:
Scientific/TechnologyAll Job Posting Locations:
Anasco Puerto Rico United States of AmericaJob Description:
Fueled by innovation at the intersection of biology and technology were developing the next generation of smarter less invasive more personalized treatments.
Are you passionate about improving and expanding on the possibilities of vision treatments Ready to join a team thats reimagining how vision is improved Our Vision team solves the toughest health challenges. Help combine cutting-edge insights science technology and people to encourage eye care professionals and patients to proactively protect correct and enhance healthy sight for life. Our products and services address these needs from the pediatric to aging eye in a patients lifetime.
Your unique talents will help patients on their journey to wellness. Learn more at the direction of the Engineering Manager handles most aspects of a project or initiative. Role is responsible for problem identification reporting root cause analysis project management financial analysis efficiency or productivity improvement reporting and problem solving. Role interfaces directly with other department 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 Project responsible.
RESPONSIBILITIES:
Leads and executes moderately to highly complex projects ensuring safety regulatory compliance and business needs are met
Optimizes process output equipment utilization waste reduction and cost management creatively.
Provides technical support for process deficiencies changes and equipment issues analyzing and resolving problems promptly.
Sets engineering standards mentors the team and challenges the status quo to develop innovative process ideas.
Collaborates across site functions and divisions during project phases.
Supports non-conformance investigations generating reports and corrective actions and troubleshooting equipment to boost production and team capabilities.
Ensures adherence to BOPs GMPs company policies and regulations; revises and maintains process documentation.
Supports GMP audits as a subject matter expert and coordinates communication with end users and suppliers.
Participates in cross-departmental projects evaluates process trends for continuous improvement and monitors manufacturing lines daily.
Provides training on process validation develops validation strategies and independently solves manufacturing issues.
Maintains compliance with environmental safety and occupational health policies.
EXPERIENCE & EDUCATION:
Bachelors degree in Engineering is required
Minimum four (4) years of experience is required in a manufacturing R&D or process development environment.
Experience in Medical Device or Pharmaceutical industry is preferred
Six Sigma certifications or equivalent is preferred
Strong expertise in Lean Manufacturing Six Sigma and other performance optimization methodologies.
Deep knowledge of medical device regulatory requirements (FDA QSR ISO 13485 EU MDR).
Experience with process validation automation and risk management.
Proficiency with CAD MES ERP systems and automation tools.
Excellent analytical problem-solving and team leadership skills.
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 and 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 email the Employee Health Support Center () or contact AskGS to be directed to your accommodation resource.
Required Skills:
Preferred Skills:
Accelerating Coaching Critical Thinking Facility Management Good Manufacturing Practices (GMP) Lean Manufacturing Principles Lean Supply Chain Management Manufacturing Engineering Performance Measurement Product Design Program Management Project Engineering Project Schedule Risk Compliance Robotic Automation Safety-Oriented Science Technology Engineering and Math (STEM) Application Technologically SavvyRequired Experience:
Senior IC
About Johnson & Johnson A t Johnson & Johnson, we believe good health is the foundation of vibrant lives, thriving communities and forward progress. That’s why for more than 130 years, we have aimed to keep people well at every age and every stage of life. Today, as the world’s larges ... View more