557 Ofertas de Qa Qc en Argentina

Join to apply for the Analista QA/QC role at Wood

Wood está en la búsqueda de un Analista QA/QC para trabajar en proyecto Minero en la provincia de Catamarca con una extensa experiencia en el campo de la industria minera para unirse a su unidad de negocio de Procesos y Químicos.

• Implementar la Política de Calidad, la Política de Seguridad y los Objetivos de Calidad requeridos por el Sistema de Gestión de Calidad
• Verificar el cumplimiento y la comprensión mediante la revisión de las presentaciones de calidad del contratista de acuerdo con los requisitos del contrato
• Trabajar con los contratistas de la construcción para garantizar el desarrollo oportuno de un Plan de inspección y pruebas (ITP) específico del contrato
• Monitorear a los contratistas de construcción para verificar que estén siguiendo sus manuales de calidad y los ITP aprobados por el proyecto
• Interactuar con clientes, proveedores y grupos internos con respecto a las inquietudes y la frecuencia de las inspecciones para garantizar que se cumplan todos los requisitos de inspección
• Realizar la vigilancia diaria del sitio, inspecciones, encuestas, auditorías y evaluaciones del proveedor / subcontratista y proporcione documentación detallada por escrito de estas actividades utilizando un formato aprobado
• Asegurar de que los inspectores de control de calidad de los contratistas realicen las inspecciones requeridas en el sitio y que los registros se archiven correctamente en los libros de datos del proyecto
• Asegurar que los recorridos del sistema y los controles de calidad aleatorios se ejecuten de manera oportuna y de acuerdo con el Paquete de trabajo de construcción (CWP), incluidos los cambiadores, y los últimos planos Emitidos para la construcción (IFC)
• Verificar que las actividades del sitio relacionadas con la calidad estén de acuerdo con los códigos y estándares aplicables
• Verificar periódicamente que el seguimiento de ensayos del contratista de construcción y los porcentajes de avances estén actualizados y sean precisos

• Conocimiento codificación de documentos, armado carpetas /Dosier
• Conocimiento de paquetes/software: Excel /Navisworks/Exagon.
• Se requiere nivel básico del idioma Inglés (No es excluyente)
• Minimo 6 Meses de experiencia
• Modalidad de trabajo bajo Roster 14 x 14

Wood is a global leader in consulting and engineering, helping to unlock solutions to critical challenges in energy and materials markets. We provide consulting, projects and operations solutions in 60 countries, employing around 35,000 people.

We are an equal opportunity employer that recognises the value of a diverse workforce. All suitably qualified applicants will receive consideration for employment on the basis of objective criteria and without regard to the following (which is a non-exhaustive list): race, colour, age, religion, gender, national origin, disability, sexual orientation, gender identity, protected veteran status, or other characteristics in accordance with the relevant governing laws.

• Entry level

• Full-time

• Quality Assurance

• Professional Services

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Santo Domingo, Santa Fe, Argentina 6 days ago

Worley es una firma global de servicios profesionales compuesta por expertos en energía, productos químicos y recursos. Nos asociamos con clientes para entregar proyectos y crear valor durante la vida útil de sus activos. Estamos uniendo dos mundos, avanzando hacia fuentes de energía más sostenibles y al mismo tiempo ayudamos a proporcionar la energía, los productos químicos y los recursos que se necesitan ahora.

• Asegurar el cumplimiento de la política de Calidad de Worley, como así también el Plan de Gestión y su aplicación durante la ejecución de la obra.

• Coordinar las actividades de cada uno de los Supervisor que conforman el departamento.

• Deberá revisar, evaluar y aprobar el Plan de Calidad del proveedor o contratista, y todos sus documentos asociados (Planes de Inspección y Ensayos, Procedimientos, Formularios/Registros, etc.)

• Participar en reuniones de programación y progreso de Fabricación/Construcción para analizar posibles desvíos o retrasos de los proveedores / contratistas por tareas propias de calidad que no se encuentren adecuadamente contempladas.

• Llevar el control de las no conformidades y las solicitudes de acciones correctivas y preventivas que surjan durante el desarrollo del Proyecto

• Efectuar recepción y evaluación final de toda la documentación de calidad (Data Books) generados por los proveedores / contratistas, para posterior entrega de estos, al cliente.

Software, procesos y herramientas:

• Experiencia mayor a 8 años en posiciones similares de proyectos mineros / Oil & Gas.

• Excelentes habilidades comunicativas e interpersonales.

• Manejo y coordinación de equipos de trabajo.

• Manejo del idioma Inglés. Deseable.

• Experiencia en Trabajo modalidad Roster en Altura.

• Manejo de sistema de gestión de calidad Norma, ISO 9001:2015.

• Se valora perfil orientado a obras de ingeniería Civil.

• Participar y liderar reuniones de calidad y contractuales con contratistas

• Evaluación KPI’s (indicadores de gestión y documentación de Calidad)

• Lugar y modalidad de trabajo: Salta en Roster 14x14.

• En caso de que necesites algún ajuste de accesibilidad por favor no dejes de aclararlo en tu postulación.

Avanzando juntos

Estamos comprometidos a construir un lugar de trabajo diverso, inclusivo y respetuoso donde todos sientan que pertenecen, puedan hablar y ser escuchados. Brindamos igualdad de oportunidades de empleo a todos los solicitantes y empleados calificados sin importar edad, raza, credo, color, religión, sexo, origen nacional, ascendencia, estado de discapacidad, estado de veterano, orientación sexual, identidad o expresión de género, información genética, estado civil. estatus, estatus de ciudadanía o cualquier otra base protegida por la ley.

Queremos que nuestra gente esté llena de energía y poder para impulsar un impacto sostenible. Por eso, nos centramos en una cultura inspirada en valores que genere brillantez a través de la pertenencia, la conexión y la innovación.

Estamos construyendo un lugar de trabajo diverso, inclusivo y respetuoso. Crear un espacio donde todos sientan que pertenecen, puedan ser ellos mismos y ser escuchados.

Y no estamos hablando sólo de eso; lo estamos haciendo. Estamos recapacitando a nuestra gente, aprovechando habilidades transferibles y apoyando la transición de nuestra fuerza laboral para convertirse en expertos en la infraestructura y tecnología de energía baja en carbono de hoy.

Cualquiera que sea tu ambición, aquí hay un camino para ti. Y no existe ninguna barrera para el posible éxito profesional. Únase a nosotros para ampliar sus horizontes, explorar diversas oportunidades y ser parte del logro de un cambio sostenible.

Job description:

Job Summary

The Quality Control (QC) Specialist is responsible for implementing, managing, and overseeing quality control processes within clinical research operations. This role ensures that all aspects of clinical trials comply with protocols, Good Clinical Practice (GCP), regulatory guidelines, and organizational standards. The QC Specialist collaborates with site staff, Clinical Trial Managers (CTMs), and other departments to verify data accuracy, maintain documentation integrity, and ensure trial readiness for audits and inspections. This role requires a strong understanding of quality standards, regulatory compliance, and the ability to identify and mitigate risks proactively.

Key Responsibilities

• Develop and oversee quality control processes at clinical research sites.
• Review data for accuracy, consistency, and compliance with study protocols.
• Conduct regular monitoring visits and ensure adherence to regulatory standards.
• Support audit readiness and collaborate with QA teams during inspections.
• Train site staff on GCP, documentation practices, and internal procedures.
• Identify quality risks and implement corrective/preventive actions.
• Prepare and maintain audit-ready documentation and QC reports.
• Collaborate with CTMs, PIs, QA, sponsors, and CROs to ensure quality standards across all trial phases

Requirements

• Proven experience in multi-site clinical trials and data verification.
• Strong knowledge of GCP, ICH guidelines, and regulatory bodies (FDA, EMA).
• Proficient with CTMS and EDC platforms.
• Excellent attention to detail, organizational skills, and communication abilities.

Tipo de puesto: Tiempo completo

Lugar de trabajo: Empleo presencial

Tipo de puesto: Tiempo completo

Lugar de trabajo: Empleo presencial

About This Role

As an Associate III, Quality Control at our laboratory in Villa Soldati CABA,

you will play a pivotal role in the Quality Control group. You will be responsible for conducting essential environmental, physico-chemical, and microbiological testing to support the release and distribution of products in Argentina. Your role will include microbial limit tests, endotoxin, sterility, and more, ensuring compliance with cGMP and local Health Authority requirements. You'll manage projects related to method transfer, qualification, and validation activities, and maintain laboratory equipment and supplies. Your expertise will guide the review of GXP documentation while fostering the development of peers through leadership modeling. Additionally, your proficiency in Biogen Quality Systems will be key for continuous improvement across Quality Systems. You will be a subject matter expert, liaising with Quality Assurance, Manufacturing, and Quality Control teams, while coordinating investigations impacting the quality areas. This role requires a mature leadership approach, excellent English communication skills, and the ability to work independently and collaboratively across all business areas.

What You'll Do

• Perform routine release testing of finished products, including microbiological testing for product release and distribution in Argentina.
• Conduct QC environmental monitoring and microbial limit tests, ensuring compliance with cGMP and local Health Authority requirements.
• Participate in and manage method transfers and analytical improvement projects.
• Provide timely review of data and documentation generated for or by QC.
• Author or review controlled documents, investigational protocols, and reports.
• Manage laboratory stock and ensure the availability of laboratory reference materials.

Who You Are

You are inquisitive and eager to learn, always questioning and seeking evidence to support your findings. Your strong understanding of quality control testing principles, combined with excellent communication and collaboration skills, enables you to work effectively across all levels of the organization. Logical thinking is your forte, making you a valuable team member who excels in both independent and collaborative settings.

Required Skills

• 2 years of relevant experience in Quality Control or related field.
• Studies in Pharmacy, Chemistry, or Biological Sciences.
• Proficiency in microbiological testing methodologies.
• Strong organizational skills and ability to multi-task and manage multiple projects.
• Advanced English. Fluency preferrred.

Preferred Skills

• Experience with FDA/EMA/HA and local regulatory compliance.
• Familiarity with small molecule testing science principles.
• Proficiency in generating purchase requisitions and processing invoices.

Job Level: Professional

We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.

At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts.

All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

Japanese Quality Control Reviewer

The Language Doctors, Inc. is a US-based linguistic services provider known for its commitment to quality and precision. We are currently seeking a detail-oriented and bilingual Japanese Quality Control Reviewer to join our team.

This role is ideal for professionals fluent in Japanese and English with a strong eye for linguistic accuracy and consistency.

Key Responsibilities:

• Monitor overall document quality to ensure adherence to client-specific and internal standards throughout the review process.

• Review linguistic content to verify grammatical accuracy, appropriate terminology, and alignment with style guides and tone requirements.

• Check formatting and layout to ensure documents follow template specifications, visual consistency, and structural completeness.

• Suggest process improvements and participate in root-cause analysis when errors are detected.

• Collaborate with team members to communicate findings and escalate quality concerns as needed.

• Ensure projects are delivered within timelines while maintaining high quality.

Qualifications:

• Native or near-native fluency in Japanese, with strong command of written and verbal English (minimum B2 CEFR level).

• Minimum 1–2 years of experience in Quality Assurance or document review, preferably in the medical or life sciences fields.

• Demonstrated attention to detail and ability to analyse complex documents for consistency and quality.

• Proficient in Microsoft Word and Excel, including formatting, comments, and revision tools.

• Strong organizational and time management skills with the ability to meet deadlines independently.

Preferred Skills:

• Experience reviewing Japanese handwritten documents and translated texts

• Background in transcription, documentation, or translation QA

Technical Requirements:

• Computer with 8GB RAM or higher

• Intel i5 (5th gen or newer) or equivalent processor

• Microsoft Office 2019 or later

• Reliable internet connection (50 Mbps minimum)

Available Schedules:

• Monday to Friday | 09:00 AM to 5:30 PM EST
• Monday to Friday | 02:00 PM to 10:30 PM EST
• Monday to Friday | 10:00 PM to 06:30 AM EST

The Language Doctors, Inc. is an equal-opportunity employer committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.

Visit our website at to learn more about us.

Korean Quality Control Reviewer

The Language Doctors, Inc. is a US-based linguistic services provider known for its commitment to quality and precision. We are currently seeking a detail-oriented and bilingual Korean Quality Control Reviewer to join our team.

This role is ideal for professionals fluent in Korean and English with a strong eye for linguistic accuracy and consistency.

Key Responsibilities:

• Monitor overall document quality to ensure adherence to client-specific and internal standards throughout the review process.

• Review linguistic content to verify grammatical accuracy, appropriate terminology, and alignment with style guides and tone requirements.

• Check formatting and layout to ensure documents follow template specifications, visual consistency, and structural completeness.

• Suggest process improvements and participate in root-cause analysis when errors are detected.

• Collaborate with team members to communicate findings and escalate quality concerns as needed.

• Ensure projects are delivered within timelines while maintaining high quality.

Qualifications:

• Native or near-native fluency in Korean, with strong command of written and verbal English (minimum B2 CEFR level).

• Minimum 1–2 years of experience in Quality Assurance or document review, preferably in the medical or life sciences fields.

• Demonstrated attention to detail and ability to analyse complex documents for consistency and quality.

• Proficient in Microsoft Word and Excel, including formatting, comments, and revision tools.

• Strong organizational and time management skills with the ability to meet deadlines independently.

Preferred Skills:

• Experience reviewing Korean handwritten documents and translated texts

• Background in transcription, documentation, or translation QA

Technical Requirements:

• Computer with 8GB RAM or higher

• Intel i5 (5th gen or newer) or equivalent processor

• Microsoft Office 2019 or later

• Reliable internet connection (50 Mbps minimum)

Available Schedules:

• Monday to Friday | 09:00 AM to 5:30 PM EST
• Monday to Friday | 02:00 PM to 10:30 PM EST

The Language Doctors, Inc. is an equal-opportunity employer committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.

Visit our website at to learn more about us.

Con un legado único en dermatología y décadas de innovación de vanguardia, Galderma es el líder emergente en la categoría de dermatología, presente en aproximadamente 90 países. Ofrecemos un portafolio innovador basado en la ciencia de marcas emblemáticas premium y servicios que abarcan todo el espectro del mercado de la dermatología en rápido crecimiento a través de Estética Inyectable, Cuidado Dermatológico y Dermatología Terapéutica. Desde nuestra fundación en 1981, hemos dedicado nuestra atención y pasión al órgano más grande del cuerpo humano, la piel, satisfaciendo las necesidades individuales de consumidores y pacientes con resultados superiores en asociación con profesionales de la salud. Porque entendemos que la piel en la que vivimos moldea nuestras vidas, estamos avanzando en dermatología para cada historia de piel.

Buscamos personas que se centren en obtener resultados, abracen el aprendizaje y traigan una energía positiva. Deben combinar la iniciativa con un sentido de trabajo en equipo y colaboración. Sobre todo, deben estar apasionados por hacer algo significativo para los consumidores, pacientes y profesionales de la salud a quienes servimos todos los días. Nuestro objetivo es empoderar a cada empleado y promover su crecimiento personal mientras se asegura de que se satisfagan las necesidades comerciales ahora y en el futuro. En toda nuestra empresa, valoramos la diversidad y respetamos la dignidad, la privacidad y los derechos personales de cada empleado.

En Galderma, damos activamente a nuestros equipos razones para creer en nuestra ambiciosa meta de convertirnos en la principal empresa de dermatología del mundo. Con nosotros, tienes la oportunidad definitiva de adquirir nuevas y desafiantes experiencias laborales y crear un impacto directo sin igual.

Objetivo Del Puesto
El objetivo del cargo es asegurar el cumplimiento de GMP/GLP en el laboratorio de control de calidad, supervisando los ensayos de nuevos productos, el correcto funcionamiento de los equipos y las áreas de seguridad e higiene. Además, se encargará de gestionar y actualizar los SOPs, así como cumplir con los planes de calidad, incluyendo calibraciones y validaciones.

Responsabilidades Principales

• Evaluar los resultados de los análisis de rutina para aprobar o rechazar productos terminados, materias primas y materiales de empaque.
• Revisar y evaluar las técnicas analíticas utilizadas, garantizando su adecuación y la validez de los resultados.
• Administrar las actividades del personal para optimizar tiempos de ejecución y asegurar la eficiencia del laboratorio.
• Participar en la redacción y actualización de SOPs (Procedimientos Operativos Estándar) conforme a la normativa vigente.
• Recomendar la compra de equipos nuevos para garantizar que el laboratorio cuente con los recursos necesarios.
• Asegurar la capacitación técnica continua de los analistas del sector.
• Supervisar el estado de calibraciones, vencimientos de reactivos y estándares, y mantener los recursos del sector en condiciones adecuadas.
• Verificar el almacenamiento de contramuestras y supervisar el muestreo de materias primas y productos terminados.

Perfil
Título de Grado
:

• Título en áreas de la salud (farmacéutico es un plus) o en campo relacionado.

Nivel De Inglés

• Inglés avanzado. Necesario para participar en reuniones con el equipo global y seguir información sobre nuevos lanzamientos.

Transferencia y Validación Analítica

• Experiencia en la transferencia y validación analítica, asegurando el cumplimiento de los protocolos establecidos por las autoridades sanitarias locales.
• Elaboración de reportes para autoridades sanitarias locales.

Conocimientos y Experiencia

• Experiencia mínima de 5 años como líder en análisis físico-químico o microbiológico.
• Al menos 8 años en el área de laboratorio.
• Idealmente, experiencia en el sector farmacéutico.

Competencias y Habilidades
Iniciativa y Anticipación
:

• Capacidad para tomar decisiones proactivas y anticiparse a las necesidades.

Espíritu De Crecimiento

• Alineación con los objetivos del negocio y enfoque en crecimiento continuo.

Comunicación y Partnering

• Habilidad en negociación, priorización y establecimiento de alianzas efectivas.

Mejora Continua

• Enfoque en identificar y aplicar opciones de mejora.
• Optimización de procesos y mejoras continuas.

Ofrecemos: Oportunidades para crecer, aprender y generar un impacto directo en el negocio. Buscamos personas apasionadas y comprometidas con hacer algo significativo en la salud y bienestar de las personas.

Únete a nosotros y haz parte de la innovación dermatológica

Job Description
KYC Analyst QC Latam supporting Commercial Banking (NA)
As part of the Quality Control team, you will be a key part of the CB business.

As a Client Onboarding Analyst, you will report to a KYC Associate or KYC Manager. You will be a key part of the CB business ensuring a comprehensive due diligent review is completed for new and existing clients in accordance with AML/KYC standards.

Core functional responsibilities and expectations include, but are not limited to, the following:

• Performing the review of client profiles, checking for consistency of the whole Lifecycle based on legal and commercial documents, to understand client´s activity, structure, and associated risks
• Obtain a general understanding of and execute AML (Anti money laundering) policies and internal procedures, in accordance with local and global principles.
• Resolve issues by identifying underlying or hidden problems and patterns
• Build knowledge of procedures, systems, products and services
• Foster partnerships with other supporting areas such as Legal, Compliance, Internal Controls, Technology, Client Services, including Global Client Onboarding teams
• Identify and control risk to prevent fraudulent account behavior and potential fraud exposure
• Prioritize daily workload to maximize productivity utilizing time management and organizational skills
• Follow all established policies, procedures and practices
• Project a confident and professional presence to all the extended teams we work with
• Work independently with supervision and escalate complex issues as necessary to resolve issues in a timely manner

Daily activities will include, but are not limited, to reviewing client profiles. Additionally, you will be expected, over time, to get involved with other activities being run within the team or within the BACC corporate center. Also, we currently operate in the hybrid work model i.e. three days in the office and two days work from home. However, in 2026 we will be return to the office full time (company directed)

Experience

• Excellent communication skills both written and verbal
• Relentless and versatile learner with an aptitude for assimilating new industry, company, product or technical knowledge
• Highly organized, proactive and motivated with strong prioritization skills, innovation and problem-solving skills
• Demonstrated, consistent professional presence with the ability to adapt to evolving needs and situations
• Sense of urgency/ability to work well under pressure and tight deadlines
• Demonstrates flexibility and willingness to accept new assignments and challenges in a rapidly changing environment, as well as handling multiple tasks and changing priorities on a daily basis
• Knowledge of tools such as Alteryx, Tableau, BI, UiPath, will be considered an asset.

Required Experience

• College degree preferred, or equivalent work experience
• Preferred minimum of one to three years of customer service, operations, sales or portfolio management experience, preferably with work experience primarily in banking or the financial service industry
• Proficient PC skills including Word, Excel and PowerPoint
• Fluent English is mandatory, both written and verbally.
• Previous experience with AML/KYC, Investment Banking, is a plus but it´s not an exclusive requirement.

About Us
J.P. Morgan is a global leader in financial services, providing strategic advice and products to the world's most prominent corporations, governments, wealthy individuals and institutional investors. Our first-class business in a first-class way approach to serving clients drives everything we do. We strive to build trusted, long-term partnerships to help our clients achieve their business objectives.

We recognize that our people are our strength and the diverse talents they bring to our global workforce are directly linked to our success. We are an equal opportunity employer and place a high value on diversity and inclusion at our company. We do not discriminate on the basis of any protected attribute, including race, religion, color, national origin, gender, sexual orientation, gender identity, gender expression, age, marital or veteran status, pregnancy or disability, or any other basis protected under applicable law. We also make reasonable accommodations for applicants' and employees' religious practices and beliefs, as well as mental health or physical disability needs. Visit our FAQs for more information about requesting an accommodation.

About The Team
J.P. Morgan's Commercial & Investment Bank is a global leader across banking, markets, securities services and payments. Corporations, governments and institutions throughout the world entrust us with their business in more than 100 countries. The Commercial & Investment Bank provides strategic advice, raises capital, manages risk and extends liquidity in markets around the world.

About This Role

As an Associate III in the Quality Control group at our Biogen Laboratory in Villa Soldati, CABA ; you will be an integral member of the Quality Control team, contributing to key functional, tactical, and operational elements. Your primary focus will be on performing QC environmental, routine physico-chemical, and microbiological testing of products to support their release and distribution in Argentina. This involves tasks such as pH measurement, appearance checks, osmolality assessments, moisture analysis (Karl-Fisher), HPLC, dissolution tests, UV identification, microbial limit tests , and other related activities adhering to cGMP and local Health Authority requirements. You will manage projects, facilitate method transfers, and oversee qualification and validation activities. Your role will ensure the maintenance of laboratory equipment and supplies, review GXP documentation, and foster leadership competencies while aiding in the development of your peers. Moreover, you will serve as a subject matter expert, ensure compliance with regulatory licenses, interface with key stakeholders in Quality Assurance, Manufacturing, and Quality Control, and coordinate investigations impacting Quality areas. Your expertise will also support Quality Management in interviewing, training employees, and driving compliance with training policies. This position requires excellent written and verbal communication skills in English and a mature leadership approach to effectively manage personal communication styles within the team framework.

What You'll Do

• Perform routine release testing of finished products, including physico-chemical analyses such as pH, appearance, osmolality, moisture (Karl-Fisher), assay and impurities by HPLC, uniformity content, dissolution tests, and UV identification.
• Participate in and manage the execution of method transfers and analytical improvement projects.
• Provide timely review of data and documentation generated for or by Quality Control.
• Author or review controlled documents, investigational protocols, investigational reports, and change control requests.
• Support laboratory stock management for the QC lab, ensuring the availability of laboratory reference materials.

Who You Are

You possess a strong understanding of quality control testing principles and are naturally curious, eager to learn, and ask questions to seek evidence-based clarity. You excel in communication and collaboration, demonstrating logical thinking and the ability to work across all organizational levels effectively.

Required Skills

• 2 years of relevant experience in Quality Control or related field.
• Studies in Pharmacy, Chemistry, or Biological Sciences.
• Proficiency in microbiological and physico-chemical testing methodologies.
• Strong organizational skills and ability to multi-task and manage multiple projects.
• Advanced English. Fluency Preferred.

Preferred Skills

• Experience with FDA/EMA/HA and local regulatory compliance.
• Familiarity with small molecule testing science principles.
• Proficiency in generating purchase requisitions and processing invoices.

Job Level: Professional

We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.

At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts.

All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.