Technical Operations Engineer II

Johnson & Johnson•San Lorenzo, PR

3d•Onsite

About The Position

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 jnj.com. 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. Under the direction of the Engineering Manager, manages and/or support most aspects of a project or initiative. Role is responsible for problem identification, root cause analysis, project management, financial analysis, project development, efficiency or productivity improvement, and problem resolution. Role interfaces directly with other San Lorenzo and Corporate functional groups to ensure that goals/objectives are met within GMP/ISO compliance and product design changes are addressed appropriately.

Requirements

Bachelor’s degree in engineering.
Related experience is required.
Bilingual (Spanish & English).
Advanced computer skills and use of software application(s) including MS Office.
Proven ability to anticipate and solve problems.
Able to manage multiple priorities.
Experience and working knowledge in short- and long-term project management.
Ability to read, analyze, and interpret general business periodicals, technical procedures, or governmental regulations.
Ability to write reports, business correspondence, and procedure manuals.
Ability to effectively present information and respond to questions from groups of managers, customers and other employees of the organization

Nice To Haves

A minimum of 3 to 5 years of experience in process improvement or maintenance engineering role in the Medical devices or pharmaceutical industry preferred.
Requires working / visiting all shifts and flexibility to work holidays, irregular hours including weekends per the operational needs.
Some traveling may be required.
Availability to work various work schedules, which may include 1st, 2nd, 3rd shifts and/or 12hour daily shifts, including weekends and holidays.

Responsibilities

Manages and executes projects and/or programs of low to medium level complexity ensuring safety, regulatory compliance, company standards, operation requirements and business needs.
Leads and/or support the optimization of process output and throughput, equipment utilization, equipment downtime, waste reduction/yield improvements, budget management, standard cost and capital investment management in an innovative manner.
Challenges the “status quo” on a routine basis and develops new ideas within incoming processes.
Work on NC Quality actions files from origination to full cycle completion and final approval.
Follows Standard Operating Procedures (SOP), Good Manufacturing Practices (GMPs), Company Policies and Federal, State and Local Government Regulations.
Develops new ideas within incoming processes.
Coordinate communications and interfaces within end users (Ethicon San Lorenzo) and machine manufacturers or suppliers.
Writes, develops, and implements validation procedures.
Plans and develops own methods.
Takes actions in the absence of specific instructions.
Develops and presents new or improved methods.
Quality - Services must be of high quality to prevent or reduce to a minimum production's downtimes.
Engaged in contacts with personnel at all levels within the organization.
Interface with appropriate manufacturing representatives to ensure manufacturing operations and projects receive effective technical support in alignment with EPS.