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BD (Becton, Dickinson and Company) Production Coordinator- in Cayey, Puerto Rico

Job Description Summary

Coordinator

Job Description

We are the makers of possible

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.

We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you’ll be supported to learn, grow and become your best self. Become a maker of possible with us.

Job Summary

The Production Coordinator- 2nd Shift is responsible to coordinate all activities related to the Fill and Pack area. Main responsibility includes line clearance activities to assure compliance as the verifier for the production records in the area. In coordination with the Planner and Area Supervisor, coordinates the production schedules, prepares the manufacturing records, and distributes them to the production area. Requests the supplies requisitions and follows up to avoid shortages in operating supplies required for the area. Will coordinate activities related to control of supplies and materials inventories. Also, will be a backup for batch records reconciliation, and revision. Follows QSR, ISO, safety and environmental regulations.

DUTIES AND RESPONSIBILITIES

  • Set up production areas. Ensure Shop Floor Papers and Transfer Orders match with respective materials.

  • Assure area orders are segregated and counted out within established control procedure.

  • In coordination with the Planner and the area supervisor, coordinates the production schedules, prepares the manufacturing records, assign work, and distributes them to the production area.

  • Perform line clearance activities and all verifications steps to assure compliance with safety regulations and quality standards for every lot processed.

  • Ensures that cleaning, inspection, maintenance, and calibration of equipment take place according to schedule. Maintains related logs and records.

  • Train operators pertaining to production processes and proper use of equipment.

  • Notify maintenance workers and Supervisor of equipment malfunctions.

  • Ensures SOP’s, GMP’s and ISO are followed throughout the manufacturing process.

  • Reconciles product and batch records. Writes clear and neat information in batch control records.

  • Requests the creation of supplies requisitions and follows up to avoid shortages in operating supplies required for the area. Monitor and expedites flow of materials (MROs) within production area.

  • Responsible for the monitoring of critical materials inventory and follows up in delivery to minimize production interruptions.

  • Ensure Shipping schedule requirements are fulfilled on time to avoid Backorders.

  • Responsible for performance of internal department cycle count on a timely manner. Reconcile variances on cycle counts and any discrepancies on production records with the finance personnel.

  • Assures that material movement transactions are executed in SAP system.

  • Support Investigations and deviations generated in their area.

  • Informs direct supervisor of developments that may affect operations or contribute to personnel issues, incidents, or accidents.

  • Support the verification steps at the Trucount Area.

  • Support Manufacturing process as needed.

  • Follows EH&S policies and procedures.

  • Actively participate in the Shift start up meeting by attending, leading shift start up meetings, and providing appropriate metrics.

  • Provide recommendations to support systems that continuously improve product/process quality and product availability, reduce cost, and increase production capability (Kaizen, ESOs)

  • Assist Biotechnology Supervisors in coordinating and monitoring activities of regular operations.

  • Perform review of production records ensuring that process was completed per procedures.

  • Apply judgment to resolve routine situations in the production areas.

  • Convey clear instructions to production personnel and communicate issues to Manufacturing Facilitator and related personnel.

  • Performs other related duties and assignments as required.

KNOWLEDGE AND SKILLS

  • Demonstrated Excellence in Quality performance

  • Working knowledge on manufacturing / production processes.

  • Working knowledge on the use of MS Windows environment software such as MS Office.

  • Knowledge of GMP, FDA, ISO and OSHA requirements.  Effective skills on analytical thinking, problem solving, interpersonal relationships and written and oral communication, planning/organization.

  • Demonstrated ability to lead.

  • Demonstrated ability to follow established policies and procedures.

  • Fully Bilingual (English and Spanish). Willing to travel to US mainland and offshore.

EDUCATION AND EXPERIENCE

Requires a minimum of Associate degree (preferable in science fields). A minimum of one year of experience in a Fill and Packaging area with demonstrated excellence in quality performance.

SUPERVISION

Coordinating and guiding the activities of non-exempt associates.

MENTAL DEMAND

Apply principles of logical or scientific thinking to define problems, collect data, establish facts, and draw valid conclusions. Manage stressful situations.

PHYSICAL DEMAND

Occasionally, the work requires carrying, lifting, pushing and pulling of light level objects. In addition, occasionally requires standing, sitting, reaching, handling and seeing (depth perception). Frequently, the job requires walking and fingering. Constantly, the work requires talking, hearing and seeing (near and far vision).

WORKING ENVIRONMENT

The work is performed constantly inside the building. The work requires exposure to extreme cold temperatures changes and hazards exposures (biomedical).

For certain roles at BD, employment is contingent upon the Company’s receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD’s Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law.

Why Join Us?

A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It’s also a place where we help each other be great, we do what’s right, we hold each other accountable, and learn and improve every day.

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 health. At BD, you’ll discover a culture in which you can learn, grow, and thrive. And find satisfaction in doing your part to make the world a better place.

To learn more about BD visit  https://bd.com/careers

Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of 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, or any other protected status.

Primary Work Location

USA PR Cayey - Vicks Drive (BDB)

Additional Locations

Work Shift

Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of 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, or any other protected status.

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