Job description
New Myrex Laboratories Inc. is actively seeking a dedicated Quality Control Analyst to join our expanding team in Malolos City, Bulacan. This full-time role is ideal for a detail-oriented laboratory professional who is passionate about product safety, quality, and regulatory compliance. You will be part of a dynamic QA/QC function committed to upholding the highest standards of quality across all stages of the product lifecycle.
In this role, you will contribute to the integrity of our manufacturing and testing processes by applying validated QC methods to raw materials, in-process samples, and finished products. You will collaborate closely with QA, Research & Development, and Manufacturing to ensure compliance with GMP and internal specifications. Your attention to detail, strong documentation practices, and proactive problem-solving will help identify, investigate, and resolve quality issues quickly, supporting continuous improvement initiatives across the organization. The position offers competitive compensation, a comprehensive benefits package, and opportunities for professional growth within a reputable laboratory that prioritizes accuracy, reliability, and teamwork.
Qualified candidates will bring a solid foundation in pharmaceutical or life sciences QC, hands-on experience with analytical methods, and a commitment to accurate data recording and compliance. If you thrive in a fast-paced lab environment and want to contribute to high-quality products that meet regulatory expectations, we invite you to apply.
Responsibility
- Develop, implement, and maintain quality control procedures for incoming materials, in-process samples, and finished products to ensure adherence to specifications.
- Perform routine analytical testing (e.g., chromatography, spectrophotometry, titrations) and interpret results with accuracy and reliability.
- Document test results, deviations, and CAPA (Corrective and Preventive Actions) in approved systems; generate clear, compliant batch records and reports.
- Calibrate, maintain, and qualify laboratory instrumentation; track calibration and maintenance schedules to ensure reliable data.
- Monitor quality metrics, conduct trend analysis, and escalate issues to QA and production teams for timely resolution.
- Participate in internal and external audits; support compliance with GMP, GLP, and safety procedures.
- Assist in investigations of non-conformances, root-cause analyses, and implementation of preventive measures.
Qualification
- Bachelor's degree in Chemistry, Pharmaceutical Sciences, or a related field.
- 1–3 years of hands-on quality control experience in a pharmaceutical or life sciences setting.
- Strong knowledge of GMP/GLP guidelines and quality systems; experience with QA/QC documentation and regulatory compliance.
- Proficiency with laboratory instrumentation (e.g., HPLC, UV-Vis spectrophotometer, pH meters) and data analysis.
- Excellent attention to detail, critical thinking, and problem-solving abilities; good written and verbal communication skills.
- Experience with laboratory information management systems (LIMS) and electronic record-keeping is preferred.
- Ability to work collaboratively in cross-functional teams and adapt in a fast-paced environment.