Analista Control de Calidad

**Analista Control de Calidad - Materias Primas**

At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where, Health for all, Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining ‘impossible’. There are so many reasons to join us. If you’re hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there’s only one choice.

When you show proactivity and ambition, we’ll harness it through a variety of opportunities and challenges in the diverse areas of our business - all with a strong and meaningful purpose. Where do you want to go? What do you want to do? How do you want to make a difference? The choice is yours, and we’ll help you get there. Be better together. Be Bayer.

**Main Purpose**

Sampling & analysis all incoming raw material samples & intermediate bulks (i.e. purchased materials, production or process technology batches). Perform standard physical and chemical analysis per the approved procedures, ensuring compliance with the written specifications.

**Your mission Will be to**
- Adhere to all aspects of Corporate and Plant safety programs, GMP’s, ISO standards or other regulatory requirements.
- Perform and support standard qualitative and quantitative analysis on Raw Materials in accordance with the approved testing procedures.
- Adhere to all Bayer and Regulatory guidelines for documentation, ensuring accurate, clear, legible and complete records of all information related to the sample login and release, analytical testing and investigations, preventive maintenance and instrument calibration, inventory and training.
- Trained/qualified on basic and various analytical techniques, instruments and equipment, for qualitative and/or quantitative analysis.
- Prepare laboratory reagent solutions for Raw Materials per monograph procedures as needed to support the laboratory. Prepare sample placebos for method development and validations.
- Perform glassware washing to support the laboratory. Distribute and maintain adequate levels of clean glassware as required for testing needs.
- Prepare and file retain samples for Raw Materials. Maintain the sample file room. Manage the monthly retains for all tested samples.
- Responsible for filing the laboratory documentation according to DI requirements.
- Assist supervisor with revising SOPs, testing procedures and training material, with non-compliance investigations for in-process work and other special assignments as directed.
- Support calibration, qualification, and maintenance of the qualified state of laboratory equipment and Systems.
- Participate in laboratory safety audits and solvent dumping schedule.
- Participate in QC weekly PSS dialogue.
- May perform other duties as assigned, including housekeeping tasks.

**Unlock your Potencial**
- Advanced/ completed university degree in science/ engineering.
- Preferably at least 2 years of GMP lab experience required, showing demonstrated ability to accurately conduct routine QC tests in accordance with approved written procedures and demonstrated ability to follow production schedule with mínimal direction from her/ his manager.
- Knowledge of and effective use of Standard Operating Procedures (SOPs) is required.
- Must be able to basically read, write, and speak English; ability to understand verbal and written instructions.
- Must have good organizational skills, high degree of accuracy in testing and completing paperwork, and legible handwriting.
- Demonstrated ability to adhere to safety and Personal Protective Equipment (PPE) is required.
- Good interpretive judgment and skills to coordinate timing of testing and material flow by following production schedule is required.
- Personal computer (PC) skills required, including skills in Microsoft Word, Excel and Laboratory Information Management systems (SAP-QM).
- Herramientas: cromatografía líquida de alta eficiencia y buenas prácticas de documentación y de laboratorio (GMP y GLP). Deseable: uso de GC (cromatografía gaseosa) Empower e inglés técnico
- Preferentemente disponibilidad para turno tarde (13.45 a 22hs). Rol 100% planta Pilar (contamos con servicio de charter)
- Experiência en Industria pharma, consumer health, veterinaria o cosmética

YOUR APPLICATION

This is your opportunity to tackle the world’s biggest challenges with us: Maintaining our health, feeding growing populations and slowing the rate of climate change. You have a voice, ideas and perspectives and we want to hear them. Because our success begins with you. Be part of something big. Be Bayer.

LI-LATAM

**Período de aplicación**:

- 19/12/2024 - 5/1/2025

**Código de referencia**:

- 836082

**División**:

- Consumer Health

**Ubicación**:

- Argentina : Buenos Aires : Pilar

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