Deskripsi Pekerjaan
Are you a detail-oriented Pharmacist with a passion for excellence in pharmaceutical production? We are seeking a highly skilled QA/QC Section Head to join our manufacturing facility in Majalengka. In this pivotal role, you will be responsible for overseeing either Quality Assurance or Quality Control operations, ensuring that all products meet stringent regulatory standards, GMP requirements, and company safety protocols.
The successful candidate will lead a team of professionals, fostering a culture of compliance and continuous improvement. You will act as a key technical authority, ensuring that the integrity of our pharmaceutical processes remains at the highest industry standards. If you are a proactive leader looking to make a significant impact on healthcare product quality, we want to hear from you.
Tanggung Jawab
- Lead and manage the daily operations of the QA or QC department, ensuring alignment with global pharmaceutical standards.
- Develop, implement, and monitor Standard Operating Procedures (SOPs) to ensure full compliance with GMP and local regulations.
- Conduct thorough internal audits and lead investigations for any deviations or non-conformance incidents.
- Manage the stability testing program, raw material sampling, and final product release processes.
- Supervise, mentor, and train junior laboratory staff and QA officers to enhance departmental expertise.
- Collaborate with Production and Supply Chain teams to troubleshoot issues and optimize quality workflows.
- Maintain comprehensive documentation and prepare analytical reports for regulatory submissions and management reviews.
Kualifikasi
- Bachelor’s Degree in Pharmacy (S1 Farmasi) and must possess a valid Pharmacist Professional Certificate (STRA).
- Minimum of 3-5 years of working experience in QA/QC within the pharmaceutical manufacturing industry.
- Deep understanding of CPOB/GMP (Cara Pembuatan Obat yang Baik) guidelines and international quality standards.
- Strong analytical, troubleshooting, and problem-solving skills, with a focus on attention to detail.
- Proven leadership capabilities with the ability to manage cross-functional teams effectively.
- Proficiency in laboratory equipment, chemical analysis, and quality documentation software.
- Ability to work effectively under pressure and meet tight production deadlines.