Quality Assurance Trainee — GMP/Pharma

F. Hoffmann-La Roche AG; Singapore; On-site; SGD 70,000 - 100,000; Full time

Job summary

Roche Singapore seeks a QA professional to provide oversight for RSTO, ensuring investigational and commercial products are manufactured in line with global Roche PQS and local site requirements.

You will perform batch record reviews, support Make, Assess, Release operations, participate in cross-functional initiatives, and escalate quality issues to senior management as needed. The role requires attention to detail, knowledge of cGMP, and flexibility to support shift work.

Qualifications

• Knowledge of cGMP and GDP in pharma
• Ability to execute defined procedures independently
• Strong problem-solving abilities
• Excellent written and verbal communication
• Proactive team player with collaborative spirit
• Flexible in work hours, including shifts
• Excellent attention to detail and organization
• Experience in biotech/pharma operating environment is a plus
• Ability to prioritize, plan and manage multiple deliverables
• Willingness to learn and adapt in a regulated setting

Responsibilities

• Perform batch record, batch reports, logbooks and audit trails reviews to ensure product quality and on-time disposition.
• Provide QA guidance on categorization of unplanned events and release of GMP areas, utilities and equipment.
• Review discrepancies and justify resuming GMP processing as needed.
• Execute Periodic Floor Walk and other QA oversight tasks.
• Notify Senior Management of potential quality, regulatory and compliance issues.

Skills

cGMP knowledge

Problem solving

Communication skills

Prioritization & planning

Analytical thinking

Team player

Flexibility / shift work

Education

Degree in Life Sciences or Engineering

Job description

Roche Singapore seeks a QA professional to provide oversight for RSTO, ensuring investigational and commercial products are manufactured in line with global Roche PQS and local site requirements.

You will perform batch record reviews, support Make, Assess, Release operations, participate in cross-functional initiatives, and escalate quality issues to senior management as needed. The role requires attention to detail, knowledge of cGMP, and flexibility to support shift work.