Snr Formulation Technician
Thermo Fisher Scientific
Work Schedule
12 hr shift/nightsEnvironmental Conditions
Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Cold Room/Freezers -22degreesF/-6degrees C, No contact lens allowed; prescriptive glasses will be provided, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Strong Odors (chemical, lubricants, biological products etc.), Warehouse, Will work with hazardous/toxic materialsJob Description
Join Thermo Fisher Scientific as a Snr Formulation Technician and embark on an exceptionally rewarding career where your work contributes to world-class advancements! Based in Singapore, you will be part of a collaborative team, working towards flawless execution of our ambitious goals. Our organization is driven by a proven strategy and a dedication to making significant contributions to the world.
ResponsibilitiesOperate pharmaceutical production equipment, including filling lines, autoclaves, washers, formulation processes, and inspection equipment, strictly following SOPs.Coordinate formulation activities for production batches, including the dispensing of drug substances and excipients.Prepare, wash, and sterilize materials and parts.Package and transfer the final product to the freezer.Complete all relevant training before performing tasks.Perform necessary materials and process (SAP) transactions at each manufacturing step.Adhere to aseptic techniques and practices for aseptic operations.Clean and maintain production equipment and classified areas within the manufacturing space.Conduct QC sampling and in-process testing at various manufacturing stages.Timely complete relevant batch records and logbooks while adhering to GDP.Transfer materials for manufacturing batches.Prepare filters for test execution and perform FIT (filter integrity testing).Load and unload equipment during production activities.Conduct stock checks of consumables and inform the Manager/Lead Technician of required materials.Follow safety and quality compliance at all times, reporting any anomalies immediately.Participate in EHS, Business Compliance, cGMP, and other compliance-related matters.Report quality issues to the Manager or Lead Technician immediately.Perform microbial sampling and swabbing of room and equipment as required.Liaise with external vendors for instrument calibration and maintenance.Perform chemical and mathematical calculations to determine product potency and endotoxin levels when required.Perform visual inspection, labeling, and packaging of finished drug products.Conduct in-process sampling and inspection of semi-finished drug products.Undertake any other duties as assigned by the Manager.EducationMinimum “O” Level, NITEC/ITE education/Diploma in a relevant field.Experience3 to 5 years of experience in the pharmaceutical industry.Knowledge, Skills, AbilitiesGood understanding of safe working practices and cGMP.Highly motivated to work in the pharmaceutical industry.Strong great teammate.Ability to work rotating shifts.
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