Biotechnologist - Manufacturing Central Operations
Found in: Talent SG 2A C2 - 2 weeks ago
Biotechnologist
to join our
Manufacturing Central Operations
group at our
Tuas
site in Singapore. Reporting to the Section Lead/Manager, you will be responsible for the manufacturing of therapeutic proteins under cGMP conditions.You will be working in 12-hour rotating shift in a 2-2 3-2 2-3 pattern and will be compensated with shift premium and allowancesKey responsibilities:Learn and perform well-defined procedures within a GMP manufacturing settingPerform equipment monitoring & and basic 6S housekeepingPerform basic laboratory tasks (e.g. sampling, pH/ conductivity/ osmolality measurements etc.)Perform routine sanitization tasks to maintain facility standardsTrained & signed off on Performance Measures (PMs) relating to CIP/ SIP/ basic tank & instrument operationsDemonstrate aseptic technique in the handling of product/ materialsPerform basic process & equipment troubleshootingMulti-task on equipment preparations & operations to ensure adherence to scheduleAttain full competency in the performance of all operations relevant to manufacturing areas assigned.Display basic process & equipment troubleshooting ability under routine scenarios.Become a technical process expert by exhibiting basic understanding of critical process/operational parameters and target/acceptable ranges, as well as interactions between different process parameters.Use Standard Operating Procedures (SOPs), logbooks & Batch Records (BRs) effectively & competentlySubmit samples via Laboratory Information Management System (LIMS)Materials & Equipment PreparationsAble to identify the correct materials by part number and FEFO lots.Select appropriate Dispensing Booths/Hoods and Weight balance.Identify sampling requirements based on material RMS.Assemble Autoclave assembly per SOP.Able to perform equipment wash without stains and residues.Solutions PreparationsEnhanced knowledge of the different setup and equipment use between customers for different operations, e.g.: CIPs and buffer/media transferAble to identify and lead the installation of the different set up and equipment for different customers for different operations, e.g.: CIPs and buffer/media transferUnderstand the criticality of setting up the right path and equipment for different customersIn depth knowledge of the different set up and the equipment use between single use and the conventional stainless steel equipmentAble to formulate plans for executing CIPs to meet different customers requirement, e.g., the CIPs of the HTST.Key requirements:Diploma/NITEC in a related Science/Engineering discipline or some relevant work experience in a similar industryKnowledge of Biopharmaceutical processing is not essential, but an added assetKnowledge of cGMP applicationsPositive team oriented attitudeStrong communication and interpersonal skillsWilling to perform rotating 12-hour shift patternEvery day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
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