QC Analyst

Overview

Join a Singapore-based regional hub for Asia Pacific and contribute to a globally recognized biopharmaceutical organization with a long-standing presence in Singapore and across AP. This opportunity sits within the Quality function, which helps ensure that every raw material, product component, and finished item is manufactured, tested, stored, packaged, and distributed in line with strict quality expectations and regulatory obligations.

The role reports to the Lab Manager, Quality Control and focuses on laboratory testing and review of raw materials, in-process samples, intermediates, final drug substances, and stability batches within Active Pharmaceutical Ingredients laboratories.

Key Responsibilities

• Carry out assigned tests and related work within required timelines while following SOPs, internal quality and safety standards, regulatory dossiers, and pharmacopoeial requirements.
• Handle calibration, routine maintenance, and qualification activities for laboratory instruments and equipment.
• Support and participate in laboratory efficiency initiatives, analytical method transfer, method development, validation work, and equipment qualification activities.
• Investigate laboratory issues such as equipment failures, out-of-trend results, and out-of-specification results, including root-cause analysis and preparation of reports.
• Review and update SOPs and laboratory test procedures as needed.
• Maintain proper laboratory housekeeping and manage inventory, including in-house stock control for reference standards, reagents, and consumables.

Additional Expectations

After approximately one year in the position, you are expected to be capable of performing most laboratory testing tasks in accordance with cGMP, data integrity, and GLP requirements. Training will cover the use of instruments and systems such as particle size analyzers, FTIR, UV-Vis spectrometers, microscopes, Empower CDS, HPLC, and GC.

Requirements

• A bachelor’s degree in Chemistry or Biochemistry is required, and previous work experience is preferred.
• 0 to 3 years of experience in pharmaceutical analysis is preferred.
• Fresh graduates may be considered if they have relevant internship exposure.
• Hands-on experience with particle size analyzers, GC, HPLC, FTIR, Karl Fischer titrators, and potentiometric titrators is preferred.
• Working knowledge of cGMP, GLP, and regulatory expectations related to pharmaceutical analytical testing is preferred.
• The position may follow standard working hours or a 12-hour rotating schedule, including day and night shifts as well as Saturdays and Sundays.
• A shift allowance will be provided if the role is assigned to shift work.

What You Can Expect

• Opportunities to grow across multiple manufacturing functions with a structured career path.
• Access to a modern facility serving customers worldwide.
• An inclusive workplace that values diverse perspectives and collaborative problem-solving.
• An equal opportunity environment committed to diversity and inclusion.
• This posting is intended to build a pipeline of talent for upcoming similar roles.

Role Note

Requisition ID: P-100901