Human Computer Interaction Internship Jobs in Puerto Rico

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 Functions:

• Reviews inspection criteria, inspection methods and procedures to assure acceptable quality standards at the most economic level

• Investigates product complaints and directs the activities required to assure the timely implementation and documentation of corrective action

• Provides support and assures cGMP compliance in product and process validations and product and process transfers

• Monitors quality trends and conducts technical and statistical investigations on quality problems, reporting the results and recommendation in a timely manner

• Performs and review IQ's, OQ's and PQ's of manufacturing, packaging, test and inspection equipment and/or process performance validations

• Conducts audits to assure compliance to BD procedures and specifications, as well as to regulatory requirements

• Plays a key role in ensuring that the Corporation and customer's quality requirements are met on assigned products, programs, areas, and functions to ensure requirements are fulfilled. This includes review operation documents, process procedures, test procedures, inspection analysis, Vendor Quality Manuals, and customer and military specifications

• Provides technical and quality support to suppliers, the Manufacturing Engineering group and to the Customer Service department on the analysis of product returned from the field

• Reviews trends and planning of overall defect reduction programs associated with their assigned products or program. Such trend information is available from formal sources, such as the quality reports and informally through frequent interaction with Supervisors, Inspectors and Production personnel

• Interacts with representatives from different groups, including Manufacturing Engineering, Purchasing, Financial Department, and all production and inspection personnel in the facility. Also, evaluates customer complaints to identify any failure trends. This may require frequent communication with Division Field Assurance Department and suppliers on quality engineering issues

• Reviews all documentation related to product quality such as test procedures, raw material, specifications, operational procedures, etc. and approves as appropriate to ensure product quality

• Improves systems, monitors performance, and identify skills, training and capabilities needed

• Monitors inspection and test results and initiate corrective actions to maintain acceptable levels

• Assures are trained before performing any task

• Uses the required clothes, personal and security protective equipment according to the requirements of its operation

• Follows the cGMP's, Quality Standards and established policies and/or procedures

• Performs other duties assigned by supervisor

Basic Qualifications:

• Must be thoroughly knowledgeable on CGMP's, ISO 13485, OSHA and familiar with other Regulatory Requirements applicable to a medical device manufacturing operation

• Must perform statistical analysis and have the ability to analyze data and communicate effectively in order to solve problems where past experience cannot necessarily be drawn upon

• Must be able to interact with different kinds of persons in a harmonious manner, being cognizant of basic corporate, divisional and departmental goals

• Must have computer programming and software applications knowledge.

• Willing to travel

• Must be bilingual (English/ Spanish) and must have good communication skills both oral and written

• Team work oriented

Education and/or Experience:

• Bachelors Degree in Engineering

• Three (3) or more years' experience in the quality control and/or validation field, in a Medical Device manufacturing facility

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.

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