QC Technician II

Work Schedule and Environment

The role follows a standard Monday to Friday schedule, from 8:00 am to 5:15 pm, based in Singapore at the Gul Circle site. The work environment requires strict adherence to Good Manufacturing Practices (GMP) safety standards typical in cleanroom conditions where no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, or facial hair are allowed. The job also involves accessing cold rooms/freezers at -22°F (-6°C), office settings, warehouses, and handling hazardous or toxic materials. Required personal protective equipment includes safety glasses, gowns, gloves, lab coats, and ear plugs.

About Thermo Fisher Scientific

Joining this team provides an opportunity to contribute to impactful work supporting a healthier, cleaner, and safer world. The company equips teams with the resources to meet career objectives while innovating solutions to global challenges such as environmental protection, food safety, and medical cures.

Job Purpose

Conduct inspections of incoming materials, take precise measurements, and review batch records to ensure full compliance with quality systems aligned with ISO 13485 and 21 CFR 820 standards.

Key Responsibilities

• Inspect incoming materials to verify they meet quality specifications and regulatory standards.
• Thoroughly review manufacturing batch records and related documentation for accuracy and completeness before approving material release or finalizing batches.
• Effectively communicate and collaborate with Manufacturing and Quality Control teams to facilitate timely material release.
• Carry out environmental monitoring, document measurements, and compile test reports following established protocols.
• Raise Nonconforming Material Reports through TrackWise and manage the segregation and proper handling of nonconforming materials per approved procedures.
• Perform inventory-related transactions in JDE software to support inspections and product release workflows.
• Maintain organized filing systems for outgoing inspection reports.
• Lead investigations and trend analyses on material and reagent failures, identify root causes, and contribute to the implementation of corrective and preventive actions (CAPA).
• Provide recommendations to improve operational processes and efficiency.
• Support Senior Technician in updating records on the daily Tier meeting Excel board.
• Undertake additional duties as assigned.

Candidate Requirements

• Education: Completion of higher secondary education, diploma, or equivalent.
• Experience: At least 1 year in Quality Assurance or Quality Control roles within regulated, cGMP-compliant environments.
• Skills: Strong written and verbal communication abilities; detail-oriented; capable of working autonomously and collaboratively; motivated and results-driven with a positive demeanor; sound analytical capabilities; familiarity with ISO standards and regulatory requirements.

Physical and Work Environment Considerations

The position requires adherence to varying environmental conditions and compliance with strict cleanliness and safety protocols as per GMP standards.

Employee Benefits

The company offers a competitive salary package, annual incentive bonuses, healthcare coverage, and an array of employee benefits. It promotes a workplace culture grounded in integrity, passion, engagement, and innovation, providing rich career development opportunities.