Quality analyst
Carmona
Job Description
Posted on 4 May 2026- Perform routine testing and analysis of raw materials, in-process samples, and finished products to ensure they meet quality standards
- Operate and maintain laboratory equipment, including analytical instruments, to conduct a variety of tests and analyses
- Document all testing procedures, results, and observations in compliance with standard operating procedures and Good Manufacturing Practices (GMP)
- Collaborate with cross-functional teams to investigate and resolve any quality-related issues
- Participate in continuous improvement initiatives to enhance laboratory processes and procedures
- Stay up-to-date with industry regulations, guidelines, and best practices in quality assurance and control
- Bachelor's degree in Chemistry, Pharmacy, Chemical Engineer, Licensed Chem Tech/Chemist/Pharmacist
- Minimum 1 year of experience as a Quality Control Analyst or in a similar role within the pharmaceutical industry
- Proficient in the use of analytical equipment and techniques, such as HPLC, GC, and UV/Vis spectrophotometry
- Strong attention to detail and critical thinking skills to ensure accurate and reliable results
- Excellent written and verbal communication skills to effectively collaborate with cross-functional teams
- Ability to work independently and as part of a team in a fast-paced, regulated environment
- Familiarity with GMP regulations and quality control procedures in the pharmaceutical industry
Work location
CARMONA, CAVITE
Remarks
No additional remarks
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