Internship in Materials CR (12 months)

Título del trabajo: Internship in Materials CR (12 months)

Compañía: Hologic

Descripción de funciones: Job Description:

• Education / Educaci贸n:
• 50% of total percentage of University bachelor’s degree in engineering, or related career.

• Experience / Experiencia:
• No experience required.

• Specialized Knowledge (Desirable) / Conocimiento especializado (preferible):
• Knowledge of FDA Medical Device Regulations including Quality System Regulation 21 CFR Part 820 (Preferable)
• ISO 13485:2016 (Preferable)
• Canadian MDR, and Medical Device Directive (Preferable)
• Equipment qualification.
• Test method and procedure development
• Statistics
• Knowledge of production processes.
• Knowledge in reading blueprints.
• Experience in equipment validation.

• Qualifications / Cualificaciones:
• Drive for Results
• Strong planning/ organizational skills
• Organizational Agility
• Listening
• Decision making
• Problem Solving

• Languages 鈥嬧�媟equired for the position (Desirable) / Idiomas requeridos para el puesto (preferible):
• Advanced English (B2+).

• Computer tools and knowledge level required (Desirable) / Herramientas inform谩ticas y nivel de conocimiento requerido:
• Microsoft Office, Internet, Minitab, Oracle, Agile, Project Management

• Responsabilities / Responsabilidades
• Give support / lead VIP / Sustaining projects.
• Support Operational Excellence program and initiatives.
• Support local and extended CSPOs, VIP projects, improvement initiatives, NPIs, product transfers, implementation of new technologies.
• Maintain, improve, and simplify procedures, processes, and methods.
• Support and promote the implementation of EHS programs to ensure people safety and environment health.
• Coordinate services with suppliers and availability of the required supplies in house. (as applicable).
• Coordinate and ensure that required payments to vendors are performed on time.
• Ensure testing, investigations are performed in accordance with the procedures and on a timely manner.
• Create and execute new procedures, new testing methods, validations.
• Make change orders.
• Follow up on change orders and projects.
• Comply with the internal policies and standards of the organization, and those stipulated in the quality system.
• Involvement and support of new product introduction activities, when required.
• Comply with safety and environmental regulations, as well as general internal policies / procedures.
• Comply with all the policies, procedures applicable to the workplace and internal regulations of the organization, and those stipulated in the quality system.
• Verify that the revision of the documents to be used, be they procedures or forms; is the most up-to-date and who is trained in it.
• Document the respective training in the training system, before executing the respective task.

• Ensure company trainings are completed on time.
• Support and/or confront and escalate issues in a timely manner.

Ubicación: Alajuela

Fecha del trabajo: Sat, 25 May 2024 06:17:51 GMT


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