Set Up Operator

BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.

1. Starts up the equipment following approved procedures. Monitors quality of product to ensure quality of production. Performs adjustments established in the approved procedures.
2. Records production information in data forms following approved procedures and in compliance with QSR, ISO 13485 and safety regulations. Ensure that data recorded is accurate, neat, and readable.
3. Ensures that environmental conditions are met in accordance with requirements of Production Specifications and data forms.
4. Notify Manufacturing Facilitator immediately of any deviations.
5. Performs equipment clean-up, changeovers, routine preventive maintenance, and trouble- shooting on equipment under his/her responsibility.
6. During production, inspects own work to ensure that it complies with requirements stated in approved procedures and forms. Removes any defective parts or product and notifies Manufacturing Facilitator immediately of any deviations observed.
7. Recognizes and brings to the attention of the Manufacturing Facilitator or Shift Leader defective components or raw materials that may cause product failure or affect equipment output.
8. Ensures proper disposition of waste materials.
9. Reconciles daily production.
10. Maintain production area clean and safe.

11. Pursue ongoing goal of cost reductions.
12. Perform other related duties as assigned by Manufacturing Facilitator.
13. Ensures that own work is performed in compliance with QSR, ISO 13485.
14. Responsible for meeting the production goals and quality of products as established by the procedures that apply to each product.
15. Manage raw materials, production supplies and work in process.
16. Comply with all documentation required following the GMP practices.
17. Use Statistical Process Control to maintain the process control of the products and meet products requirements.
18. Make use of the 5S to keep the machine and area clean and organized.
19. Report any safety hazard to the supervisor.
20. Participate of the decisional process and must perform their functions with or without direct supervision.
21. Keep the equipment and tools in optimal conditions; these include daily maintenance and preventive maintenance.
22. Report to engineering and/or to maintenance of any machine malfunction.
23. Differentiate between electronic and mechanical malfunctions in order to direct the engineering and maintenance department.
24. Evaluate the effectiveness of the preventive maintenance and recommend changes as necessary.
25. Perform SAP transactions of the material use in the manufacturing process.
26. Perform any other duties assign by the production supervisor.

Education and Experience:
1. Technical Certification on Industrial Mechanic, Electronics, or any related industrial certification, or minimum of 6 months demonstrated proficiency on SM equipment’s.
2. Two years (2) of experience in the medical device, and/or pharmaceutical, or cosmetic Industry.
3. Preferably bilingual (Spanish & English).

Knowledge and Skills:
1. Knowledge in MS Office and design program.
2. Working knowledge in electronics, hydraulic, pneumatic, and mechanical systems.
3. Able to read and understand drawings and schematics.
4. Able to communicate, be a team player, initiative. Should be efficient and effective in the search for solutions.

3rd Shift Availability

5pm - 5:30am