Quality Control Manager

Description Can you spot issues, problems, or anomalies quickly? If so, you could be a fit for this exciting role! As a Quality Control Manager, you'll have an impact across various functions of our supply chain. You will be doing work that matters to our business and operations and is essential to everything we hold dear. If our product isn't up to the highest quality standards, we need you to tell us and help us make things better.We are seeking a highly skilled and expert Quality Control Manager to join our pharmaceutical QC Lab team in Indonesia where communication, initiative, leadership, collaboration skills, and abilities are important.Our QA team strives for nothing but the best every single day. It's one of the key reasons over 5 billion consumers purchase our products around the world. On our team, you'll play a key part in driving the integrity of our brands and helping us deliver our Quality Promise: "Quality our consumers, customers, regulators, and employees trust - everywhere, every time."Key Responsibilities Team Leadership: Lead and develop a team of QC analysts and technicians, providing mentorship, training, and support to ensure efficient and effective lab operations.Quality Control: Implement and maintain a robust quality control program, including the development and revision of standard operating procedures (SOPs), technical standards (test methods, specifications), and protocols.Compliance: Ensure strict adherence to local and international pharmaceutical regulations (BPOM/CPOB) and guidelines (WHO, ICH) in all QC activities.Instrumentation: Lead all aspects of the calibration, maintenance, and qualification of QC analytical instruments and equipment.Testing and Analysis: Coordinate and conduct various analytical tests and assays to evaluate the quality, purity, and potency of pharmaceutical products, including HPLC, Spectrophotometer, Dissolution Tester, etc.Data Management: Review, analyze, and maintain accurate records of test results, ensuring data integrity and compliance with documentation requirements.Investigations and Deviations: Lead investigations of out-of-specification (OOS) results and deviations, implement corrective and preventive actions (CAPA) and report findings to the leadership team.Continuous Improvement: Find opportunities for process optimization and efficiency improvements within the QC Lab. Implement 5S and other operational excellence toolsSupplier and Material Management: Collaborate with procurement and supply chain teams to ensure the quality of raw materials and components used in pharmaceutical manufacturing. Ensure all suppliers and materials are qualified prior to GxPs use, including laboratory chemicals, reference standards, etc.Audit Readiness: Prepare the QC Lab for internal & external inspections and audits, ensuring readiness and compliance with all audit requirements.Job QualificationsDegree in Pharmacy (certified Apothecary).Proven Min. 5 to 7 years in pharmaceutical quality control & QC lab operations.Prefer 2 years in a managerial or leadership role, managing a team of QC Analysts.In-depth knowledge of pharmaceutical quality control regulations and guidelines.Strong analytical and problem-solving skills.Excellent communication and leadership abilities.Proficiency in laboratory instrumentation and analytical techniques.Detail-oriented with a strong dedication to quality and compliance.Job ScheduleFull timeJob NumberR000090651Job SegmentationExperienced Professionals (Job Segmentation)