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QC Technician Trainee - Attach & Train program

Roche
Central Region, Singapore
Salary Estimate
SGD 2.600 – SGD 3.200
Posting Time
1 Mei 2026
Deadline
1 Mei 2027

Job description

Roche Singapore is pleased to offer a dynamic QC Technician Trainee position within our Attach & Train program. This structured, immersive track is designed to develop the next generation of quality control professionals in a modern pharmaceutical environment. You will gain hands-on experience in a regulated lab, guided by experienced QA and Manufacturing scientists, with mentorship to accelerate your growth.

Throughout the program, you will build core QC skills, learn GMP-compliant workflows, and understand the importance of data integrity and safety in every product we deliver. Our training approach emphasizes practical, real-world testing, meticulous documentation, and collaboration with cross-functional teams to ensure product quality and timely release. This role is ideal for ambitious individuals who are early in their careers or recent graduates seeking a clear path to advanced QC roles within a global biotechnology leader.

Join Roche to develop a strong scientific foundation, gain exposure to state-of-the-art QC methods, and advance within a company known for manufacturing excellence, scientific rigor, and a commitment to patients around the world.

Responsibility

  • Participate in Roche's Attach & Train program to develop foundational QC competencies under supervision.
  • Assist with sample preparation, testing, labeling, and data entry in accordance with SOPs and GMP guidelines.
  • Support instrument setup, calibration, maintenance, and basic troubleshooting of QC equipment.
  • Record test results accurately in LIMS/ELN, ensuring data integrity and traceability.
  • Maintain a clean, organized laboratory workspace and comply with safety and waste disposal policies.
  • Contribute to quality documentation, deviation reports, CAPA processes, and continuous improvement initiatives.
  • Collaborate with manufacturing, QA, and other teams to support timely product qualification and release.
  • Learn and apply SOPs, change controls, and regulatory requirements to daily tasks.

Qualification

  • Diploma or bachelor’s degree in Chemistry, Biology, Biotechnology, or a related science field, or equivalent practical experience.
  • Fresh graduates or early-career candidates welcomed; strong willingness to learn and grow.
  • Excellent attention to detail, data accuracy, and robust documentation habits.
  • Basic knowledge of laboratory safety, GLP/GMP principles, and SOPs.
  • Proficient computer skills and familiarity with data entry; experience with LIMS/ELN is a plus.
  • Effective communication and teamwork abilities; able to follow instructions and work well under supervision.
  • Proactive problem-solving mindset and a drive for continuous improvement.

Required Skills

Quality Control GMP GLP Laboratory Techniques Instrument Calibration Data Entry Documentation SOP Adherence LIMS ELN Quality Assurance

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