Deskripsi Pekerjaan
Are you a detail-oriented professional with a passion for precision? New Myrex Laboratories Inc. is seeking a dedicated Quality Control Analyst to join our expanding team in Santa Maria, Bulacan. In this role, you will be the final line of defense in ensuring our manufacturing processes meet the highest standards of safety, quality, and regulatory compliance.
As a Quality Control Analyst, you will work closely with production and laboratory teams to monitor, test, and analyze products at various stages of the manufacturing lifecycle. We are looking for an individual who thrives in a fast-paced environment and possesses the analytical mindset required to identify process improvements, document deviations, and ensure that every product leaving our facility exceeds client expectations.
If you are committed to excellence and eager to contribute to a company that values integrity and professional growth, we invite you to apply today.
Tanggung Jawab
- Conduct routine inspections and testing of raw materials, in-process samples, and finished goods to ensure adherence to quality specifications.
- Perform comprehensive laboratory analysis using standardized methodologies and laboratory equipment.
- Document all test results, observations, and non-compliance issues accurately in accordance with Good Manufacturing Practices (GMP).
- Identify, investigate, and report any quality deviations or manufacturing inconsistencies immediately to the production supervisor.
- Maintain laboratory equipment, ensuring all tools are calibrated, clean, and functioning optimally.
- Collaborate with cross-functional departments to implement corrective and preventive actions (CAPA).
- Ensure compliance with all local health, safety, and industry-specific regulatory standards.
Kualifikasi
- Bachelor’s degree in Chemistry, Biology, Chemical Engineering, or a related science-based field.
- Minimum of 1-2 years of experience in a Quality Control or laboratory setting within the manufacturing industry.
- Proficiency in using analytical laboratory instrumentation and documentation software.
- Strong understanding of Good Manufacturing Practices (GMP) and ISO quality management systems.
- Excellent analytical, problem-solving, and critical thinking skills.
- High level of attention to detail and ability to work with minimal supervision.
- Effective communication skills, both written and verbal.