Production Operator (Multiple Positions)

Johnson & Johnson Innovative Medicine•San Lorenzo, PR

1d•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. The MedTech and Surgery teams are fueled by innovation at the intersection of biology and technology, developing the next generation of smarter, less invasive, more personalized treatments. This role is for a Production Operator who will work under the direct supervision of a Department Facilitator, performing functions in various manufacturing areas according to specifications, “GMP / QS Regulation” Good Manufacturing Practices, Safety Rules, and the Employee Manual. The operator will configure and operate automated, semi-automatic, and/or manual equipment, make adjustments, changes, and perform preventive maintenance as needed. The position involves a period of training, qualification, and a learning curve.

Requirements

A minimum of a High School diploma is required.
At least one (1) year of experience is required.
Availability to work overtime, various work schedules, which may include 1st, 2nd, 3rd shifts and 12-hour daily shifts, including weekends and holidays is required.
Ability to lift up to 30 pounds is required.

Nice To Haves

Basic knowledge of computer skills and the use of their applications (Microsoft Windows, MES, HMI, etc.) is preferred.

Responsibilities

Configure and operate automated, semi-automatic and/or manual equipment in accordance with the specifications of the process.
Verify products on the assembly line to confirm that they are correctly assembled and eliminate defective products.
Cleaning the work area to avoid contamination and / or mixing of products.
Execute basic preventive maintenance, responsible for basic equipment troubleshooting and general machine problem correction to minimize downtime, must notify supervisor of necessary equipment maintenance and/or repairs.
Product assembly according to the specifications and “GMP’s or “QS Regulation ”of the Area.
Prepare and complete the documentation of the different manufacturing steps as established by the specifications of the area.
Batch Reconciliation (“Batch”) and transfer of material to the appropriate areas.
In processes or departments where the Certified Operators system is implemented, the Associate will be responsible for inspecting and disposing of the product according to the Quality Assurance Plan.
Use personal protective equipment according to specifications, to perform the work in a safe manner.
Participate in process improvements of project activities as assigned. This may require; identification of areas of opportunity, revisions of specifications, participation in development activities, etc.