Deskripsi Pekerjaan
Am-Europharma Corporation, a premier name in the Philippine pharmaceutical industry, is seeking a detail-oriented and highly skilled Quality Control Analyst to join our dynamic team in Calamba City, Laguna. As a key member of our Quality Assurance department, you will play a critical role in safeguarding the integrity and safety of our products, directly impacting the health and well-being of our consumers.
At Am-Europharma, we pride ourselves on our commitment to international quality standards. We are looking for a professional who is passionate about precision, compliance, and continuous improvement. In this role, you will be at the forefront of our manufacturing process, ensuring that every batch of raw materials, in-process samples, bulk products, and finished goods meets stringent regulatory and company specifications before reaching the market.
Your expertise will be vital in maintaining our reputation for excellence. You will work in a state-of-the-art laboratory environment, utilizing advanced analytical techniques to perform chemical and physical testing. This is not just a job; it's an opportunity to grow your career in a company that values scientific rigor, offers stability, and provides a clear path for professional development. Join us in our mission to deliver safe and effective healthcare solutions to the Filipino people and beyond.
If you have a keen eye for detail, a strong background in chemistry or microbiology, and a desire to make a real impact in the pharmaceutical industry, we want to hear from you. Take the next step in your career with Am-Europharma Corporation.
Tanggung Jawab
- Conduct accurate and timely analysis of raw materials, in-process samples, bulk products, and finished pharmaceutical products in accordance with established analytical procedures and pharmacopeial standards (USP, BP, Ph. Eur.).
- Perform chemical, physical, and microbiological testing using laboratory instruments such as HPLC, GC, UV-Vis Spectrophotometer, pH meter, and dissolution apparatus.
- Document all test results meticulously in laboratory notebooks and computerized systems (e.g., LIMS) to ensure full traceability and compliance with Good Laboratory Practices (GLP) and cGMP.
- Prepare and standardize volumetric solutions, reagents, and mobile phases as required for laboratory operations.
- Review and verify analytical data generated by junior analysts or lab technicians to ensure accuracy and reliability before release.
- Investigate out-of-specification (OOS) results and non-conformances, perform root cause analysis, and implement corrective and preventive actions (CAPA).
- Calibrate and maintain laboratory equipment, ensuring all instruments are functioning within specified parameters and preparing maintenance logs.
- Ensure strict adherence to safety protocols, environmental regulations, and quality management systems (ISO 9001:2015) within the laboratory.
Kualifikasi
- Bachelor's Degree in Pharmacy, Chemistry, Biochemistry, Chemical Engineering, or a related life science field. Registered Pharmacist (RPh) or Licensed Chemist is an advantage.
- Proven experience (1-3 years) as a Quality Control Analyst in a pharmaceutical, food, or cosmetic manufacturing company is required.
- Strong working knowledge of analytical chemistry, quality control procedures, and Good Manufacturing Practices (GMP).
- Proficiency in operating and troubleshooting analytical laboratory instruments (e.g., HPLC, GC, FTIR, Dissolution Tester).
- Excellent attention to detail, analytical thinking, and problem-solving skills with the ability to work independently and in a team.
- Effective verbal and written communication skills in English and Filipino for accurate documentation and inter-departmental coordination.
- Willing to work in Calamba City, Laguna, and can start immediately.
- Must be amenable to shifting schedules, extended hours, and holiday work when required by production demands.