Quality Control Specialist

Job Responsibilities:

• Lead and oversee daily quality control operations for bulk, in-process, and finished products to ensure compliance with internal specifications and regulatory standards.
• Coordinate and monitor third-party manufacturers to ensure adherence to quality standards and approved processes.
• Prepare and review reports on product verification and inspection results.
• Develop, revise, and implement Standard Operating Procedures (SOPs), specifications, and testing methods in alignment with GMP and company requirements.
• Conduct investigations on Out-of-Specification (OOS), Out-of-Trend (OOT), and non-conformance results, including root cause analysis and CAPA implementation.
• Collaborate with Production, R&D, and Packaging teams to resolve quality issues and support product development and scale-up activities.
• Coordinate with manufacturing teams on production planning to ensure product availability and stock readiness.
• Support stability studies, method validation/verification, and continuous improvement initiatives.
• Manage and coordinate QC operational requirements to ensure effective product verification activities.

• Bachelor’s degree in Pharmacy, Chemistry, Chemical Engineering, Bioprocess Engineering, or a related field.
• Minimum 2-3 years of experience in Quality Control within the cosmetics or pharmaceutical industry.
• Strong knowledge of QC testing methods, including physicochemical analysis, with basic understanding of microbiological and stability testing.
• Good understanding of GMP, CPKB, ISO 9001, ISO 22716, and regulatory requirements related to cosmetic/pharmaceutical products.
• Proven experience in handling OOS, OOT, deviation investigations, and CAPA implementation.
• Familiar with laboratory instruments (e.g., pH meter, viscometer, vacuum leak tester) and their calibration and maintenance.
• Strong analytical thinking and problem-solving skills with high attention to detail.
• Ability to collaborate effectively with cross-functional teams (e.g., Production, R&D, Regulatory).
• Good communication skills in Bahasa Indonesia and English, both written and verbal.
• Experience in audit preparation (internal/external) is preferred.
• Willing to be placed in Batu Ceper, Tangerang, and able to join immediately (ASAP).