QC Specialist (Non-shift Role)

Roche Diagnóstica Brasil; Singapore; On-site; SGD 50,000 - 80,000; Full time

Job summary

Roche recherche un Spécialiste QA pour assurer la qualité de ses produits pharmaceutiques. Ce poste impliquera des tests analytiques, l'amélioration des méthodes, et la collaboration au sein d'une équipe performante. Vous aurez l'occasion de travailler dans un environnement stimulant qui priorise la qualité et le respect des normes. Rejoignez une entreprise qui valorise votre expertise et offre une carrière riche en possibilités.

Qualifications

• Expérience de 1 à 3 ans en contrôle qualité dans un environnement réglementé GMP.
• Connaissance pratique des opérations de laboratoire analytique et des systèmes de qualité.

Responsibilities

• Effectuer des tests analytiques de routine et non-routine de produits.
• Documenter et rapporter les résultats des tests en conformité avec les normes de qualité Roche.

Skills

Habilité d'analyse

Résolution de problèmes

Collaboration

Education

Diplôme en biochimie, chimie ou discipline scientifique liée

Job description

Na Roche, você pode-se apresentar como você mesmo, abraçado pelas qualidades únicas que traz. Nossa cultura incentiva a expressão pessoal, o diálogo aberto e as conexões genuínas, onde você é valorizado e respeitado por quem você é, e permitindo que você prospere tanto pessoal como profissionalmente. É assim que pretendemos prevenir, deter e curar doenças e garantir que todos tenham acesso aos cuidados de saúde hoje e nas gerações futuras. Junte-se à Roche, onde cada voz é importante.

A posição

Join Roche and play a vital role in ensuring the quality and safety of our pharmaceutical products. As a QC Specialist, you will support the core of our manufacturing operations through accurate and timely product testing, data integrity, and continuous improvement in a hands-on, lab-based role where scientific precision meets real-world impact.

This is a regular Monday to Friday, 8:00 AM to 5:00 PM position, offering stability, predictability, and work-life balance while supporting critical business operations.

The Opportunity

You Will

• Perform and review routine and non-routine analytical testing of in-process and final product samples to support manufacturing timelines.
• Document, verify, and report test results in compliance with cGMP, SOPs, and Roche/Genentech quality standards.
• Support lab operations including housekeeping, equipment upkeep, inventory management, and reagent preparation.
• Contribute to continuous improvement initiatives, including method optimization, process enhancements, and implementation of new technologies.
• Troubleshoot testing issues and lab equipment, initiating and supporting investigations where necessary.
• Author and revise SOPs, test methods, and lab documents to maintain accuracy and compliance.
• Train and support team members in lab procedures, best practices, and quality systems.
• Participate in cross-functional projects such as method validation, method transfer, and equipment qualification.
• Lead or support discrepancy investigations, identify root causes, and define corrective actions for lab-related issues.
• Ensure all GMP training is completed in a timely and compliant manner.
• Actively contribute to a safe and compliant working environment, adhering to all Safety, Health, and Environment (SHE) requirements.
  
  

What Makes This Role Unique

• Be part of a collaborative, high-performing team that values knowledge sharing and mutual support.
• Gain exposure to global quality standards and contribute to impactful work with real patient outcomes.
• Build a solid foundation for long-term career growth in quality and manufacturing within a world-leading biotech company.
  
  

Who You Are

You're detail-oriented, hands-on, and passionate about delivering quality in every task. You’re looking for a role where your expertise and initiative make a daily difference.

You Bring

• A degree in biochemistry, chemistry, or a related scientific discipline.
• 1–3 years of QC or lab experience in a GMP-regulated environment, preferably in biotech or pharmaceuticals.
• Practical knowledge of analytical laboratory operations, cGMP, and quality systems.
• Familiarity with laboratory safety protocols and equipment maintenance.
• Strong problem-solving skills, and the ability to work independently and in teams.
• Excellent written and verbal communication skills in English.
• A proactive mindset focused on collaboration, ownership, and continuous improvement.
  
  

Quem nós somos

Um futuro mais saudável nos leva a inovar. Juntos, mais de 100 mil funcionários em todo o mundo se dedicam ao avanço da ciência, garantindo que todos tenham acesso à saúde hoje e nas próximas gerações. Nossos esforços resultam em mais de 26 milhões de pessoas tratadas com nossos medicamentos e mais de 30 bilhões de testes realizados usando nossos produtos de diagnóstico. Nós nos capacitamos para explorar novas possibilidades, promover a criatividade e manter as nossas ambições altas, para fornecer soluções de saúde que mudem a vida e causem um impacto global.

Vamos construir juntos um futuro mais saudável.

A Roche é um empregador que pratica políticas de igualdade de oportunidades.