Johnson & Johnson Vision, a member of the Johnson & Johnson Family of Companies, is recruiting for a Process Engineer located in its manufacturing site at Añasco, Puerto Rico.
At Johnson & Johnson Vision, we have a bold ambition: to change the trajectory of eye health. That’s why, through our operating companies, we’ve developed solutions for every stage of life—to help people see better, connect better and live better. We partner with eye care professionals to provide some of the world’s leading products and technologies to address refractive error, cataracts, dry eye, and beyond. We are committed to using our reach and size for good, and strive to put quality eye care within reach of everyone, everywhere. Visit us at www.jjvision.com. Follow @JNJVision on Twitter and Johnson & Johnson Vision on LinkedIn.
Under the direction of the Engineering Manager, handles most aspects of a project or initiative. Role is responsible for problem identification, root cause analysis, project management, financial analysis, efficiency or productivity improvement, 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 production goals are met.
Key Responsibilities:
•Leads and executes projects and/or programs of low to moderate level of complexity insuring 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 the Production areas in evaluating process deficiencies, process changes, modifications and equipment failure. Defines, analyzes, reviews and evaluates problems for prompt solutions.
•Challenges the “status quo” on a routine basis and develops new ideas within incoming processes.
•Coordinates 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). Work on nonconformance files from origination to full cycle completion and final approval.
•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.
•Support the GMP audits as subject matter guide for product and processes.
•Coordinates communications and interfaces within end users and machine manufacturers or suppliers.
•Participates in projects involving other departments and activities.
•Evaluates process trends (Ex. Yield, OEE) to drive improvements of business results.
•Create and execute validation strategics.
•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
Education:
A minimum of a Bachelor Degree in Engineering is required. Industrial Engineer/Process Engineer BS degree preferred.
Experience and Skills:
•Strong organizational, interpersonal, oral and written communication skills- required.
•Ability to effectively present information and respond to questions from groups of managers, customers and other employees of the organization- required.
•Ability to prioritize multiple tasks and time management- required.
•Ability to shift priorities according to changes in department/facility needs and be open to different ideas/approaches- required.
•Strong knowledge on statistics, problem solving and lean tools required.
•Computer skills and use of software application(s). Strong computer background (MS Office, MS Project Management, Word, Excel, Outlook, etc.)- required.
•Ability to write technical reports and procedure manuals - required.
•Experience on Medical Device or Pharmaceutical industry is preferred.
Language & Travel:
Fluent on Spanish & English
10% Domestic or International Travel
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.
Primary Location
United States-Puerto Rico-Anasco- Organization
AMO Puerto Rico Manufacturing, Inc. (Branch) (7239)
Job Function
Engineering
Requisition ID
2005871806W
