1.564 Ofertas de Empresas Que Contratan Mystery Shoppers en Argentina

Location: Argentina, Australia, Canada, France, UK, US

Report to: Operations Director

Summary: We are among the top e-commerce brands in the world engaging with millions of consumers and global fashion influencers. We have built multiple platforms and brands through innovative marketing and merchandising strategies that connect with the next generation and redefine fashion retail. We strive for success and creativity to become the top e-commerce fashion brand globally. With a team based in four locations in the US, we are motivated to elevate fashion to the next level. We seek positive, proactive problem solvers who love fashion and can work independently in a fast-paced, evolving environment.

About the Position: This role is responsible for ensuring all finished products, from samples to production, meet the highest standards. The candidate will lead a small team, provide feedback on imperfections, and collaborate with the Buying team on vendor performance.

This is an on-site role; safety protocols are in place, including daily temperature checks, masks, and social distancing in warehouses, offices, and recording studios.

Quality Control Management: 7 years (Preferred)

Quality Control: 5 years (Preferred)

We are committed to recruiting, training, and promoting all associates regardless of gender, race, religion, age, disability, sexual orientation, nationality, or ethnicity. Diversity is encouraged. Discrimination, harassment, and bigotry are not tolerated.

Location: Argentina, Australia, Canada, France, UK, US

Report to: Operations Director

Summary: We are among the top e-commerce brands in the world engaging with millions of consumers and global fashion influencers. We have built multiple platforms and brands through innovative marketing and merchandising strategies that connect with the next generation and redefine fashion retail. Our goal is to hire candidates that are positive go-getters and problem solvers who love fashion. The right candidate should be able to work independently in a fast-paced and evolving environment.

About the Position: This role will be responsible for ensuring that all finished products from samples to production are of the highest standards and will lead a small team. You will provide timely feedback to the team on any imperfections and collaborate with the Buying team on vendor performance.

This is an on-site role; however, we adhere to safety protocols to keep all employees safe. Daily temperature checks and masks are required, and team members are working in a distanced manner throughout our warehouses, offices, and recording studios.

• Quality Control Management: 7 years (Preferred)
• Quality Control: 5 years (Preferred)

We are committed to recruiting, training, and providing career advancement to all associates regardless of gender, race, religion, age, disability, sexual orientation, nationality, or social or ethnic origin. Diversity in the workplace is encouraged. Bigotry, racism, and any form of harassment or discrimination are not tolerated.

Location: Argentina, Australia, Canada, France, UK, US

Report to: Operations Director

Summary: We are among the top e-commerce brands in the world engaging with millions of consumers and global fashion influencers. We have built multiple platforms and brands through innovative marketing and merchandising strategies that connect with the next generation and redefine fashion retail. We strive for success and creativity to maintain our position as the top e-commerce brand in the world. Our team, based out of four (4) locations in the US, is motivated to take Fashion to the next level. Our goal is to hire candidates who are positive go-getters and problem solvers with a passion for fashion. The right candidate should be able to work independently in a fast-paced and ever-evolving environment.

About the Position: This role will be responsible for ensuring that all finished products, from samples to production, meet the highest standards, as well as leading a small team. You will provide timely feedback to the team on any imperfections and collaborate with the Buying team on vendor performance.

1. Measure, inspect, and provide feedback about quality to the TOP team when comparing TOP samples to bulk production.
2. Identify defects effectively and efficiently, sorting defective merchandise into appropriate categories.
3. Perform, report, and communicate feedback on vendor evaluations.
4. Negotiate quality discounts with vendors.
5. Collaborate with Buying to ensure fit and quality integrity from TOP to bulk production.
6. Clearly communicate with vendors in writing and/or verbally regarding defective and unacceptable merchandise.
7. Interpret and implement quality assurance standards.
8. Collect, create, and compile information to provide reporting on all inspection results, vendor scorecard data, and communicate to organization members.
9. Coordinate and support on-site audits conducted by the internal team.

1. Comprehensive understanding of flat garment measuring, garment construction, and quality control/assurance.
2. Knowledge of preparing and writing product specification sheets.
3. High level of attention to detail.
4. Ability to identify apparel flaws quickly and effectively.
5. Ability to work successfully with any personality type.
6. Sense of urgency and ability to maintain performance quality under pressure.
7. Ability to prioritize work and follow instructions.
8. Team-oriented; ability to excel in a team-based structure.
9. Strong communication skills (verbal and written) and organizational skills.
10. Self-starter, multi-task oriented, and the ability to resolve issues in a timely manner.
11. Strong computer skills including Microsoft Office and databases.
12. 3 to 5 years of leadership experience.

1. A fun and fulfilling place to work.
2. Competitive pay.
3. 401k retirement savings plan.
4. Yearly handbag allowance.
5. Job Type: Full-time.
6. Disability Insurance.
7. Employee Discount.
8. Health Insurance.
9. Life Insurance.
10. Paid Time Off.
11. Vision Insurance.

Day shift, Monday to Friday.

This is an on-site role; however, we adhere to safety protocols to keep all employees safe. Daily temperature checks and masks are required, and team members are working in a distanced manner throughout our warehouses, offices, and studios.

Quality Control Management: 7 years (Preferred)

Quality Control: 5 years (Preferred)

We are committed to recruiting, training, and providing career advancement to all associates regardless of gender, race, religion, age, disability, sexual orientation, nationality, or social or ethnic origin. Diversity in the workplace is encouraged. Bigotry, racism, and any form of harassment or discrimination are not tolerated.

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.