Deskripsi Pekerjaan
Lonza is looking for a dedicated and meticulous Quality Control Analyst to join our world-class manufacturing facility in Tuas. As a global leader in the life sciences industry, Lonza provides a dynamic environment where quality and precision are at the forefront of everything we do. This role is essential in maintaining the integrity of our production processes, ensuring that every batch of life-saving medicine meets the highest safety standards before reaching patients.
In this position, you will work within a high-tech laboratory environment, collaborating with cross-functional teams to support our manufacturing goals. You will be responsible for the rigorous testing of raw materials, in-process samples, and final products. We are seeking a professional who thrives in a regulated cGMP environment and is committed to continuous improvement and operational excellence. If you are passionate about science and quality assurance, Lonza offers the perfect platform to grow your career and make a meaningful impact on global health.
Tanggung Jawab
- Perform timely testing and analysis of raw materials, in-process samples, and final product batches.
- Strictly adhere to Standard Operating Procedures (SOPs) and ensure full compliance with current Good Manufacturing Practices (cGMP).
- Document all analytical results accurately in the Laboratory Information Management System (LIMS) and physical logbooks.
- Maintain, calibrate, and troubleshoot laboratory equipment such as HPLC, GC, and spectrophotometers.
- Participate in laboratory investigations, including Out of Specification (OOS) and Out of Trend (OOT) results.
- Support internal and external audits by ensuring the laboratory is in an audit-ready state at all times.
- Assist in the validation and transfer of analytical methods.
- Contribute to safety and environmental initiatives within the laboratory and manufacturing site.
Kualifikasi
- Bachelor’s degree in Chemistry, Biochemistry, Biotechnology, or a related scientific discipline.
- Minimum of 1-3 years of experience in a Quality Control laboratory, preferably within the pharmaceutical or biomanufacturing industry.
- Strong working knowledge of cGMP regulations and international pharmacopoeia standards (USP, EP, JP).
- Hands-on experience with analytical instrumentation, specifically HPLC and Gas Chromatography.
- Excellent attention to detail and a high level of accuracy in data recording and reporting.
- Ability to work effectively both independently and as part of a collaborative team in a fast-paced environment.
- Strong problem-solving skills and the ability to handle technical challenges with a proactive mindset.