Junior Quality Assurance Inspector

Main purpose and objective of the position:

• Ensure that quality systems directly related to materials, purchased semi-finished products, and finished products are managed in accordance with established quality standards.

• Ensure that the material inspection of packaging, medicinal products, vials, purchased semi-finished products, and finished products is carried out in accordance with established processes, conforming to approved specifications and within the required deadlines.

Key responsibilities:

• Ensure that the review, approval, and detection of possible rejections of packaging material and the review, approval, and detection of possible rejections of purchased semi-finished products, vials, bulk products, and medicinal products are carried out adequately for their subsequent use in production.

• Carry out the identification of purchased semi-finished products prior to their receipt, as well as the sampling of bulk products for their receipt and analysis.

• Collaborate in the drafting and review and/or draft the area's GMP procedures in accordance with the standards for which we are responsible.

• Ensure communication of quality issues to the rest of the Incoming & Product Disposition Quality Assurance team members, and other Quality Assurance teams.

Key responsibilities:

- No experience required.

Personal skills:

The following qualities are required:

• Interpersonal skills: teamwork, customer orientation (internal/external), decision-making, good oral and written communication.

• Organizational skills: ability to prioritize objectives.

• Computer skills: knowledge of common office software at a user level, as well as knowledge of the computer systems that control business processes.

• Technical skills: knowledge of Good Manufacturing Practices, quality concepts, and their application in the pharmaceutical industry is valued.

Education requirements (studies):

Higher Degree in Quality Analysis and Control.

Schedule:

Night shift, 24/7.

full-time

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work-but it's work worth doing. If you're driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.

#WeAreLilly

Propósito principal y objetivo del puesto:

• Asegurar que los sistemas de calidad directamente relacionados con materiales, semiterminados comprados, y producto terminado se gestionan de acuerdo con los estándares de calidad establecidos.

• Asegurar que la inspección material de acondicionamiento, productos sanitarios, viales, semiterminados comprados y producto terminado se realiza de acuerdo a los procesos establecidos, conforme a las especificaciones aprobadas y en los plazos requeridos.

Responsabilidades clave:

• Asegurar que se realiza adecuadamente la revisión, aprobación y detección de posibles rechazos de material de acondicionamiento y la revisión y detección de posibles rechazos de semiterminados comprados, viales, graneles, y productos sanitarios, para su posterior uso en producción.

• Realizar la identificación de los semiterminados comprados previa a su recepción, asi como los muestreos de graneles para su recepción y análisis.

• Colaborar en la elaboración y revisión y/o elaborar los procedimientos GMP del área conforme a los estándares que son nuestra responsabilidad.

• Asegurar la comunicación de problemas de calidad al resto de miembros del equipo de Garantía de Calidad Incoming & Disposición de producto, y otros equipos de Garantía de Calidad.

Responsabilidades clave:

- Experiencia no requerida.

Habilidades personales:

Se requiere tener las siguientes cualidades:

• Habilidades interpersonales: trabajo en equipo, orientación al cliente (interno/externo), toma de decisiones, buena comunicación oral y escrita.

• Habilidades organizativas: cualidades para priorizar objetivos.

• Manejo de herramientas informáticas: conocimientos de software ofimático de uso común a nivel usuario, así como conocimiento de los sistemas informáticos que controlan los procesos de negocio.

• Habilidades técnicas: valorable conocimiento en las normas de correcta fabricación, en conceptos de calidad y en su aplicación en la industria farmacéutica.

Requerimientos de formación (estudios):

Grado Superior en Análisis y Control de Calidad.

Horario:

Turno 24/7 nocturno.

full-time

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work-but it's work worth doing. If you're driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.

#WeAreLilly