Attach and Train Trainee - Quality Control

Overview

This is a part-time, onsite Attach and Train position based in Tuas, Singapore, within Lonza's Quality Control team. The training program spans 15 months, focusing on practical, structured on-the-job training at the site to build essential competencies for pharmaceutical manufacturing roles.

Work Environment

The role is fully based at the Tuas site to support precise, real-time collaboration required for producing medicines that meet top quality and safety standards. The working schedule involves a rotating 12-hour day shift.

Key Responsibilities

• Execute prioritized testing and analyses promptly to align with business needs.
• Conduct analysis on final products, in-process materials, raw materials, and environmental samples adhering to Standard Operating Procedures and Test Methods.
• Document and review testing outcomes in compliance with current Good Manufacturing Practices (cGMP).
• Perform general laboratory duties including housekeeping, equipment upkeep, inventory management, procurement of lab supplies, handling of glassware, and autoclaving.
• Manage sample logistics including storage of retention samples, coordination with external laboratories, control of QC documents, and shipment of QC specimens.
• Prepare and maintain standards and reagents following GMP guidelines.
• Comply with data integrity principles consistent with company policies and proactively seek improvements in data management processes.
• Apply spectroscopy techniques and other assigned analytical methods such as chromatography (HPLC), total organic carbon (TOC), protein concentration measurements (A280 or SoloVPE), osmolality, and appearance assessment.
• Contribute actively to continuous improvement and operational efficiency efforts.
• Fulfill additional duties as assigned by management.

Candidate Profile

• Holds a degree in a relevant science discipline or possesses equivalent qualifications.
• Open to individuals without prior work experience in biopharmaceutical manufacturing.
• Basic understanding of mammalian cell culture techniques used for biopharmaceutical production.
• Familiarity with current Good Manufacturing Practices (cGMP) regulations.
• Demonstrates strong problem-solving and analytical capabilities.
• Exhibits effective communication and collaborative teamwork skills.
• Willing to work in a rotating 12-hour shift schedule.

Perks & Benefits

• Exposure to a dynamic work culture supporting career agility.
• Inclusive and ethical workplace environment.
• Daily company shuttle service between MRT locations near employees' homes and the Tuas facility.

About Lonza

Lonza is a leading global life sciences company operating over 30 sites worldwide with a commitment to collaboration, accountability, excellence, passion, and integrity. Diversity and inclusion are core to its work environment, and employees contribute to advancing innovative therapies that impact millions of lives.