Analyst II - QC

Novartis; Singapore; On-site; SGD 80,000 - 100,000; Full time

Job summary

A leading pharmaceutical company in Singapore is seeking a Quality Associate to support activities within the Quality department. The role involves managing sample storage, analytical testing, and ensuring compliance with cGxP standards. Candidates should have a background in pharmacy or chemistry with up to four years of experience in a laboratory environment. The company emphasizes collaboration and offers a community-oriented workplace.

Qualifications

• Previous experience in a laboratory environment in the pharmaceutical industry preferred.
• Knowledge of TQM and related industry GxP standards is essential.
• Experience in GMP and HSE compliant processes.

Responsibilities

• Manage sample storage and analytical testing.
• Ensure compliance with cGxP and data integrity.
• Detect and report potential risks and propose solutions.

Skills

Laboratory equipment

Quality Control (QC) Testing

Quality Control Sampling

Breakthrough Analysis

Operational Excellence

Continuous Learning

Digital & Tech Savvy

Education

University degree in Pharmacy or Chemistry

Job description

Summary

Supports all activities within the assigned Quality department. Contributes to the implementation, maintenance, and execution of the assigned Quality and/or Laboratory Systems in an effective and compliant manner.

About the Role

Key Responsibilities:

• Sample storage and management.
• Analytical testing and documentation of API / drug substance / drug product / finished product / Complaints / stability / packaging material samples.
• Ensure all activities in compliance with cGxP, including data integrity.
• Stability (when not centralized)
  • Testing/Sample storage and management.
  • Analytical documentation of stability samples to cGxP standards.
• Detect and report potential accidents, risks and propose solutions.

Essential Requirements:

• Preferred: Previous experience working in a laboratory environment in the pharmaceutical industry (quality assurance, production), aseptic technique.
• Administrative activities and GMP and HSE compliant, efficient production and documentation of standardized tasks in the infrastructure.
• Breakthrough Analysis; Being Resilient; Operational Excellence; Continuous Learning; Digital & Tech Savvy.
• Laboratory equipment; Quality Control (QC) Testing; Quality Control Sampling; knowledge of TQM and related industry GxP standards and processes; Laboratory Excellence; Quality decision making.

Desirable Requirements:

• University degree or equivalent experience in Pharmacy or Chemistry or equivalent + 0‑4 years working experience.

Why Novartis:

Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

Benefits and Rewards:

Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards

Commitment to Inclusion

Novartis is committed to building an outstanding, inclusive work environment and diverse teams representing the patients and communities we serve.