Pharmaceutical Technician (Drug Product)
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Esco Lifesciences Group provides enabling technologies, products and services to the life sciences and healthcare industries, supporting academic research and scientific discoveries, clinical practice, as well as biopharmaceutical R&D and manufacturing. Headquartered in Singapore, Esco has an extensive sales network in over 100 countries, direct sales and service offices in over 24 countries, 8 manufacturing and R&D hubs in the US, Europe, the UK, China, Singapore, Indonesia, and over 1500 employees worldwide.
Esco is poised to benefit from the sustained growth of the healthcare and biopharma industries in Asia and globally. Esco has achieved market leadership in China, and globally, in multiple categories within some of the fastest-growing segments — with China being its largest and fastest growing market. As a Singapore-headquartered company, Esco is a nexus of East and West, bridging technologies, products and talent across the world, with global operations spanning the US, Europe and Asia.
You will be part of Esco Aster’s Manufacturing team and contribute to the overall site mission and objectives. You will ensure pharmaceutical operation activities and tasks are planned and executed in an efficient and compliant manner, while adhering to cGMP standards. You will work with the Leadership team of Manufacturing to develop a continuous improvement mindset and engage in teamwork with cross-functional departments.
We are looking for someone equipped who has excellent organizational skills and the ability to prioritize their workload.
Primary work location: Ayer Rajah Crescent, Singapore
- Complete pharmaceutical operation and documentation following ALCOA principles and SOP.
- Meet the KPIs for the department and organization.
- Setup and operate the production equipment including high-speed filling machines, isolators, and compounding tanks.
- Preparation of filling machine parts including manual washing and start sterilization cycles in ovens and autoclaves
- Provide operation support on equipment/system IQ/OQ/PQ.
- Support investigation by providing information to investigator.
- Dispense, compound, and fill active biological product batches.
- Perform filter integrity testing using automatic filter integrity test unit
- Microbial sampling and swabbing of room and equipment during operation
- Complete the batch documentation as required.
- Perform visual inspection, labeling and packaging on semi-finished drug products.
- Perform in-process sampling on semi-finished drug products
- Report and discuss with supervisors regarding any problem arising during the manufacturing process, which may lead to stoppages.
- Report and investigate if any.
- Always ensure strict adherence to GMP requirements.
- Author and revise relevant SOPs, logbooks and other relevant documents.
- Higher Nitec or Diploma in Chemical, Mechanical and electronical engineering.
- Minimum 2 years of working experience in pharmaceutical manufacturing.
- Good knowledge in applying regulatory guidelines especially in manufacturing process, validation, change control cGMP and GDP
Apply now by submitting a Cover Letter and CV to [email protected].