Senior Maintenance Supervisor - 2nd shift-8272140630
Description
Janssen Ortho LLC, a member of Johnson & Johnson's Family of Companies, is recruiting a Senior Maintenance Supervisor for their facility located in Gurabo, Puerto Rico. The ideal candidate for this role should have expertise in controls for the manufacturing and packaging areas and experience managing the implementation of automation projects. This role offers a great opportunity to grow into a managerial position.
Janssen Ortho LLC., provides medicines for an array of health concerns in several therapeutic areas, including: attention deficit hyperactivity disorder (ADHD), cardiovascular disease, general medicine (acid reflux disease, infectious diseases), mental health (bipolar I disorder, schizophrenia), neurologic (Alzheimer's disease, epilepsy, migraine prevention and treatment), pain management, and women's health. Our ultimate goal is to help people live healthy lives. We have produced and marketed many first-in-class prescription medications and are poised to serve the broad needs of the healthcare market - from patients to practitioners, from clinics to hospitals. For more about Janssen Pharmaceuticals, Inc., one of the Pharmaceutical Companies of Johnson & Johnson, visit http://www.janssenpharmaceuticalsinc.com/
The Senior Maintenance Supervisor is accountable for detecting and resolving supply chain constraints related to manufacturing and packaging equipment with special focus on automation strategies, equipment optimization and equipment reliability striving in the overall support of the operations area performance. Supervises maintenance technicians, manages process equipment projects and leads equipment-related continuous improvement initiatives with new technology transfer and qualifications. Maintains in good operational conditions all Manufacturing Processing Equipment (ETF, MEX and OROS, Quicksolv, Packaging, Inspire and TSMA). Leads and represents the Operations Process Engineering Group in all automation related strategies (short and long term master plan) where the operation equipment and operating systems are impacted. Works with the site automation and controls team to provide technical support in the daily troubleshooting and resolution of controls problems in the equipment of different business units (IR, ER, Packaging, Quicksolv, Inspire). Provides technical support to the utilities controls and software applications that have direct impact in the operations areas. Develops, recommends, and supports the implementation of new controls and automation strategies including new technologies and software applications. Participates in the design and implementation phase of continuous improvement projects toward controls optimization. From the Change Management standpoint will be responsible for the detail specification and the interface with operational groups to generate full Processing Equipment requirements and successful implementation. Evaluates process and equipment and recommends appropriate modifications and/or new equipment for the improvement of the Process Centered Organization equipment considering ergonomic, environmental and safety company policies. Evaluates and implements strategic processing technology upgrades. Implements continuous improvement projects using statistical tools to minimize process variability. Represents Operations and Maintenance organization in management forums as required. Develop and maintain Statistical Analysis of the operations events and deviation trends to determine and develop process enhancements to prevent recurrence of them.
Qualifications
A minimum of a Bachelor’s Degree in Engineering is required; Mechanical and Electrical Engineering majors are highly preferred. A minimum of ten (10) years of applicable experience within regulated manufacturing environment (pharmaceutical or medical devices) is required. At least five (5) years of supervisory experience are required. Experience with clean utilities and maintenance of process equipment is required. Engineer-in-Training (EIT) certification is required; Professional Engineer (PE) license is highly preferred. Experience working with Automation, Controls and overall Maintenance areas of a regulated manufacturing facility is required. Must have experience with manufacturing and packaging processes, GMP’s, equipment/process validation, investigations, and regulatory compliance. Experience working with cross-functional project and support teams, serving different employee populations. Must be proficient in the use of Microsoft Office (Word, Excel, PowerPoint and Outlook) and Trackwise. Knowledge of Maximo and DocSpace is preferred. Must be fully bilingual (English and Spanish) – write and speak. Must possess analytical and process skills. Must have excellent technical writing skills. Availability to travel in and outside Puerto Rico approximately twenty percent (20%) of the time, if required.
BE VITAL in your Career, Be seen for the talent you bring to your work. Explore opportunities within the Johnson & Johnson Family of Companies.
J2W:LI
Primary Location:North America-United States-Puerto Rico-Gurabo
Organization: Janssen Ortho LLC (2162)
Relocation: Eligible No
Job Function: Industrial Manufacturing
Certain sites within the Johnson & Johnson Family of Companies participate in E-Verify as appropriate in accordance with Company guidelines and federal or state law. To learn more about the government sponsored program and to see a list of the sites that are currently enrolled, please click here.
Johnson and Johnson Family of Companies are equal opportunity employers, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, protected veteran status, or disability status, or any other characteristic protected by law.
EEO is the Law
EEO is the Law GINA Supplement