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 Med Tech, a member of Johnson & Johnson's Family of Companies, is recruiting for a Staff Manufacturing Engineer. This position will be located in Añasco, Puerto Rico.
Under the direction of the Engineering Manager, handles most aspects of a project or initiatives. Role is responsible for providing advanced engineering, design, and construction of manufacturing facilities, systems, and equipment; and providing engineering and technical support for complex production and processing equipment. As well as managing 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 Role Responsibilities- Develops process excellence techniques to identify systematic issues. Tracks trends, develops and implements equipment and/or process enhancements that will improve efficiency, product yield, and equipment reliability.
- 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.
- Provides technical support to peers and production areas in evaluating process deficiencies, process changes, modifications, and process optimization. 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. Reviews evaluations and advice on the selection of suitable equipment for optimized, balanced line performance and makes final recommendations to management.
- 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).
- Follows Standard Operating Procedures (SOP), Good Manufacturing Practices (GMPs), Company Policies and Federal, State and Local Government Regulations.
- Writes, develops, and execute 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
QualificationsRequired Skills:- Bachelor's Degree in Engineering
- Minimum of 6 years of experience is required in a maintenance manufacturing environment, R&D or Process Development
- Demonstrated experience in Project Management
- Proven experience with validation cycle (FAT, IQ, OQ and PQ)
- Must be fully bilingual: Spanish & English
- Proficiency with Microsoft Office: Word, Excel, PowerPoint
Preferred Skills:- Preferred experience with data analysis tools: Minitab
- Experience working at medical device industry or pharmaceutical preferred
Other:- This position will require up to 10% travel
- The attendance policy for this requisition is Fully Onsite
