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Work Background
ElektaProject Manager Far East
May. 2023 - Mar. 2025Indonesia
Alere HealthOperations Support Manager
Apr. 2021 - Jan. 2022Jakarta Raya, Indonesia
Abbott IndonesiaTPM Manager
May. 2018 - Mar. 2021Jakarta, IndonesiaManage Third Party Manufacturing which have mutual agreement with Abbott Indonesia
GlaxoSmithKline IndonesiaProject Manager
Jun. 2013 - Apr. 2018-Develop and maintain relationships between related functions, commercial entities and external suppliers to ensure Product Transfer project timelines are met and commercial / manufacturing supply strategies are achieved. -Support the development and execution of sourcing strategy plans for the Indonesian supply network. -Manage the engagement of new suppliers and provide a leadership role to both internal teams and external suppliers in the establishment of new supply networks and/or new product launches. -Implement transfer planning systems and methodologies to support product transfer projects and align ways of working with key stakeholders and global NPI & NetChange practices. -Support and maintain compliance and governance systems for the product transfer and/or NPI launch process. -Represent the Product Transfer and/or NPI projects to functional groups, workshops and above country stakeholders as required. -Support the achievement of strategic objectives and targets for the Indonesian business. -Ensure project financial cost budgets are adhered to. -Ensure leadership HPB’s are in place and in use. - Manage related related functional transition plan for divestment project in timely manner.
PT. Glaxo Smith KlineProduct Transfer Manager
Jan. 2011 - Apr. 2018• Liaises & coordinates with Production, QA, regulatory & logistics to develop an integrated Product Transfer plan, documenting the delivery strategy & success criteria • Assumes responsibility for driving & implementing the product transfer plan, communicating issues, risks & progress to project stakeholders. Specifically liasing with Logistics & Commercial to continuously review stock build & write off plans as well as liasing with Senior Management & HR to ensure all related activities are managed on a timely basis • Designs, the project organisation structure, defines team member roles and assigns individual work responsibilities. Monitors, appraises, and upgrades individual and team performance as required, to assure project success. • Ensures the technical trial, commissioning & validation strategy is in place • Implements strict project controls including procedures for change control / management, cost control / forecasting • Develops a risk management strategy for the project and implements associated processes and tools to ensure effective identification, monitoring and management of project risk
AstraZeneca IndonesiaTechnical Manager / SHE and Validation Coordinator
Jul. 2009 - Dec. 2010To establish SHE management system across Indonesian Marketing Company. To maintain SHE management system and adopt new initiatives of SHE improvements. To promote SHE across Indonesian region to ensure adequate level of SHE awareness on Marketing Company. To establish Quality Management System across Indonesian Marketing Company. To maintain Quality Management System and to keep the system on the updated status. To keep SHE and Quality record and documentation are well maintained and updated. To ensure documentations are indexed, traceable and well stored. To arrange documents are auditable. To deal with contractors around technical matters such as packaging, procedure and manufacturing. To define contractor's KPI and manage their performance. To manage manufacturing/packaging changing. To manage technology transfer in technical area. To address technical issue and resolve it properly. To develop, analyse, reviews, summarizes and maintain cGMP technical/validation documentation. To work proactively with other departments to ensure cGMP documents are accurate and comply with company and local authority's regulation. To lead and consult on multiple projects. To anticipate and assess/prevent: technical problems from impacting product, adequacy of proposed corrective actions to address root cause. 2. Jan - Sept 2008 Head of Bulk Production T area, P.T. Sandoz Indonesia (ex. Bayer Schering Pharma plant). Job description: manage product transfer activities, generate URS (User Requirement Specification) for product tooling, to be person in charge if responsible pharmacist was not in place.
Sandoz IndonesiaHead of Bulk Production
Jan. 2008 - Sep. 2008manage product transfer activities, generate URS (User Requirement Specification) for product tooling, to be person in charge if responsible pharmacist was not in place.
Bayer Indonesia Ps. Rebo PlantHead of Production Section/Production Responsible Pharmacist
Apr. 2007 - Dec. 2007monitor and improve the current GMP practice in production area, monitor and control the production process change management, generate and implement SOP, batch record review and release of products, conduct training for production and packaging personnel, maintain validity of production processes and system, schedule daily and weekly production process based on production order, appointed as Production Responsible Pharmacist according to Indonesian regulatory, coordinate with Technical Service Department to ensure preventive maintenance of machine was inline with production schedule, coordinate with third party to maintain cleanliness of production area, conduct production process risk assessment, conduct monthly sampling of hazardous airborne (API) in production area, identify suitable personnel protective equipment (PPE) for production/packaging process (mask, cloth, glove, goggle, earplug/earmuff and safety shoes). build Good Manufacturing Process (GMP) culture on production process, update and implement Quality Management System on production area, as co-auditor, to conduct internal audit within manufacturing division,
Schering IndonesiaHead of Production Section/Production Responsible Pharmacist
Sep. 2005 - Mar. 2007monitor and improve the current GMP practice in production area, monitor and control the production process change management, generate and implement SOP, batch record review and release of products, conduct training for production and packaging personnel, maintain validity of production processes and system, schedule daily and weekly production process based on production order, appointed as Production Responsible Pharmacist according to Indonesian regulatory, coordinate with Technical Service Department to ensure preventive maintenance of machine is in line with production schedule, coordinate with third party to maintain cleanliness of production area, conduct production process risk assessment, conduct monthly sampling of hazardous airborne (API) in production area, identify suitable personnel protective equipment (PPE) for production/packaging process (mask, cloth, glove, goggle, earplug/earmuff and safety shoes
Schering IndonesiaProduction Responsible Pharmacist
Aug. 2004 - Aug. 2005appointed as Production Responsible Pharmacist according to Indonesian regulatory, monitor and improve current Good Manufacturing Practice implementation in production, monitor and control the production process change management, feedback material consumption/reconciliation data to computer system, generate and review SOP and Master Batch Record, assist Head of Production Section to conduct production/packaging process risk assessment, identify suitable personnel protective equipment (PPE) for production/packaging process (mask, cloth, glove, goggle, earplug/earmuff and safety shoes), create gowning procedure to enter manufacturing areas.
Schering IndonesiaProduction Supervisor
Aug. 2001 - Jul. 2004plan and execute daily and weekly bulk production and packaging process, prepare of raw and packaging material, dispensing, granulation, tablet coating, primary packaging and secondary packaging, supervise production and packaging process and personnel, feedback material consumption/reconciliation data to computer system, deliver training (GMP and SOP) to related personnel within manufacturing division, assist Head of Production Section to conduct production/packaging process risk assessment, identify suitable personnel protective equipment (PPE) for production/packaging process (mask, cloth, glove, goggle, earplug/earmuff and safety shoes), NON FORMAL EDUCATION March 2009 Pharmacist Competency Certificate issued by ISFI (Ikatan Sarjana Farmasi Indonesia). August 2008 Weighing in Quality Management System Seminar held by Sartorius Indonesia. July 2008 Critical Aspect of HVAC for Pharmaceutical Industry Seminar held by QA-QC Managers. September 2007 GMP Seminars "Towards product quality and regulatory compliance in the manufacture of oral medicinal product" held by National University of Singapore. Apr 2006 Creating Disciplined People and Bright Factory trough 5S, training held by Productivity & Quality Management Consultants (PQM). March 2005 Refresh Fire Fighting Training, held by internal QES (Quality, Environment and Safety) Department of PT. Schering Indonesia. Jan 2005 Training of formulation, granulation, tablet pressing and tablet coating, held by P.T. Korsch Indonesia. Oct 2004 Refresh First Aider Training, held by Health Surveillance Services. July 2004 Fire Fighting Training, held by Dinas Pemadam Kebakaran DKI Jakarta. March 2003 First Aider Training, held by Health Surveillance Services. June 2002 First Aid Training 2nd Level held by SOS International.
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