Set Up Operator

Becton Dickinson; Añasco (PR); On-site; USD 28,000 - 42,000; Full time

Job summary

Becton, Dickinson and Company (BD) in Anasco, Puerto Rico, seeks a Set Up Operator to run production machinery, perform line clearances, inspections, and routine maintenance. The role requires adherence to QSR, ISO 13485, and safety rules while contributing to continuous improvement initiatives.

Responsibilities include documenting production data, supporting troubleshooting, and ensuring product quality and environmental conditions meet specifications. Strong team collaboration is essential.

Qualifications

• Technical Certification in Industrial Mechanic, Electronics, or related field.
• Two years of experience in medical device/pharma/cosmetic industry preferred.
• Bilingual in Spanish & English preferred.

Responsibilities

• Start up equipment following approved procedures and monitor product quality.
• Record production data and ensure accuracy per procedures and quality standards.
• Maintain environmental conditions per production specifications and data forms.
• Notify supervisor immediately of any deviations or equipment issues.
• Perform routine maintenance, changeovers, and cleaning of designated equipment.

Skills

MS Office

Electronics

Hydraulic systems

Pneumatic systems

Reading schematics

Teamwork/initiative

Education

Technical Certification in Industrial Mechanic or Electronics

Tools

SAP

Job description

We are the people who give possibilities purpose 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.

Job Summary

Under the direct supervision of the Manufacturing Facilitator, Set Up Operator operates production machinery and auxiliary equipment in accordance with written procedures. Performs set-ups, line clearance, product inspection, mechanic repairs, adjustment, and troubleshooting and equipment preventive maintenance and clean up. Maintain equipment in good working condition and clean. Perform routine troubleshooting. Notify Manufacturing Facilitator of any deviation from normal operation of equipment requiring maintenance support. Participate in evaluation and troubleshooting of equipment, Conduct on the job training of other associates. Participate in all team meetings, activities, team building initiatives, and continuous improvement activities. Follow approved procedures and in compliance with QSR, ISO 13485 and safety rules regulations.

Job Responsibilities

• 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

Required Skills Optional Skills . Primary Work Location USA PR - Anasco Additional Locations Work Shift We are the #MakersofPossible Working together, we make products that patients, families and their healthcare professionals rely on. We do this because we are committed to advancing the world of health™. But it takes the imagination and passion of all of us at BD, from manufacturing to marketing, to look at the impossible and find solutions that turn dreams into possibilities with real-life health benefits for people today, tomorrow and beyond. We make this happen, together. We are the makers of possible.

Why Join Us?

To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you’ll discover a culture in which you can learn, grow and thrive. We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success. To learn more about BD visit https://bd.com/careers.

Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.