Job Openings
QC Analyst | Pasir Gudang
About the job QC Analyst | Pasir Gudang
Company Background
Our client is a leading provider of chemical manufacturing and technology solutions, serving global customers in the crop protection, pharmaceutical, specialty chemicals, and engineering technology industries. With nearly 40 years of industry experience, the company is committed to delivering innovative, integrated services and technical solutions throughout the entire product lifecycle. From process development and scale-up to commercial manufacturing, they work closely with customers to meet their evolving needs at every stage, helping accelerate innovation and achieve long-term success.
Our client provides customized solutions for complex chemical processes and high-value products. The company operates 8 chemical manufacturing sites, 3 equipment manufacturing facilities, and 3 R&D centers across China, as well as production facilities in the United Kingdom and Malaysia.
Job Descriptions
- Raw Material Testing: Adhere to validated standards and SOPs; complete identification, content, and impurity tests.
- In-Process Sample Analysis: Follow validated analytical methods and SOPs; accurately fill out analytical raw records.
- Finished Product Testing and Release: Conduct comprehensive testing; prepare standardized inspection reports.
- Execute optimization and validation protocols for analytical methods (specificity, linearity, accuracy, precision).
- Lead transfer and replication of new product analysis methodologies; support R&D process optimization.
- Simple instrument maintenance; pre-use calibration of titrators, moisture analyzers.
Job Requirements
- Diploma or Degree in chemical analysis, applied chemistry, or related discipline.
- More than 3 years of analytical working experience.
- Basic analytical lab skills: titration, sample preparation.
- Proficient in HPLC, GC, HS-GC, FTIR, GC-MS, UV-VIS, Automatic Potentiometric Titrator (HPLC and GC must be proficient).
- Able to perform basic equipment maintenance and analytical method transfer/validation.
- Familiarity with Chinese Pharmacopoeia, European Pharmacopoeia, US Pharmacopeia, and GMP.