Deskripsi Pekerjaan
Are you an experienced Quality Control professional with a passion for pharmaceutical excellence? Anvita Pharma Indonesia is seeking a dedicated and proactive QC Chemical Supervisor to join our growing facility in Karawang. In this pivotal role, you will be the guardian of our quality standards, ensuring that all laboratory instruments, analytical equipment, and supporting tools are fully operational, calibrated, and compliant with international pharmaceutical regulations.
As our QC Chemical Supervisor, you will lead a team of analysts, fostering a culture of precision, safety, and continuous improvement. You will play a vital role in the production lifecycle by guaranteeing that the technical infrastructure supporting our chemical analysis processes is always ready to meet the demands of high-volume pharmaceutical manufacturing. We are looking for a leader who is detail-oriented, technically proficient, and capable of driving operational excellence within the Quality Control department.
Tanggung Jawab
- Supervise day-to-day operations within the QC laboratory, ensuring all chemical testing is performed according to SOPs.
- Oversee the maintenance, calibration, and readiness of all analytical instruments (e.g., HPLC, GC, Spectrophotometers).
- Coordinate with the engineering and procurement teams to ensure the availability of essential laboratory tools and reagents.
- Analyze deviations in equipment performance and implement prompt corrective and preventive actions (CAPA).
- Maintain rigorous compliance with cGMP, ISO, and local BPOM regulations.
- Train and mentor junior QC analysts on laboratory safety, analytical methods, and equipment troubleshooting.
- Prepare technical documentation, reports, and audit trails related to equipment qualification and validation.
Kualifikasi
- Bachelor’s degree in Chemistry, Pharmacy, Chemical Engineering, or a related field.
- Minimum of 3-5 years of experience in a QC supervisory role within the pharmaceutical or chemical manufacturing industry.
- Deep understanding of cGMP, GLP, and pharmacopoeia standards (USP/BP).
- Proven expertise in analytical instrument qualification (IQ/OQ/PQ) and maintenance management.
- Strong problem-solving skills and ability to manage multiple laboratory projects simultaneously.
- Fluency in Bahasa Indonesia and professional proficiency in English.
- Willingness to be based in Karawang, Jawa Barat.