Formulation Technician

Thermo Fisher Scientific Inc.; Singapore; On-site; SGD 20,000 - 60,000; Full time

Job summary

Thermo Fisher Scientific is seeking to hire personnel for pharmaceutical production roles in Singapore. The position involves operating vital production equipment, ensuring compliance with safety regulations, and contributing to the quality assurance processes. Candidates should possess a minimum of 'O' Level, NITEC, or a relevant diploma, demonstrating readiness to work in a manufacturing environment under strict good manufacturing practices (GMP).

Responsibilities

• Setup and operate pharmaceutical production equipment including high-speed filling lines for sterile products, autoclaves, parts and vial washers, depyrogenation tunnel, formulation process, HMI, and automatic CIP/SIP processes.
• Responsible for formulation activities of production batches, including formulation and/or dispensing of drug substances and excipients.
• Responsible for parts preparation, washing, and sterilization of materials.
• Responsible for packaging and transfer of the final product to the freezer.
• Follow aseptic techniques and practices for aseptic operations.
• Timely complete batch records and logbooks, adhering to GDP.
• Participate in EHS, Business Compliance, cGMP, and other compliance-related matters.

Education

Minimum 'O' Level, NITEC/ITE education, or Diploma in relevant field.

Job description

Work Schedule

Rotational shift nights/weekends

Environmental Conditions

Able to lift 40 lbs. without assistance, adherence to all Good Manufacturing Practices (GMP) safety standards, and specific cleanroom requirements such as no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair, etc. Allowed conditions include working in Cold Room/Freezers at -22°F/-6°C, exposure to loud noises from equipment/machinery, and working with hazardous/toxic materials. No contact lenses allowed; prescriptive glasses will be provided. PPE such as safety glasses, gowning, gloves, lab coat, ear plugs, etc., are required. The environment may involve strong odors from chemicals, lubricants, biological products, etc., and some office work.

Job Description

When you’re part of the team at Thermo Fisher Scientific, you’ll do important work surrounded by collaborative colleagues. You’ll have the support and opportunities that only a global leader can give you. Our organization has an outstanding strategy for the near term and beyond. Take your place on our strong team and help us make meaningful contributions to the world.

The incumbent will perform various tasks and activities listed below, for which they are appropriately trained and in compliance with cGMP, company and department SOPs, and safety regulations.

Responsibilities

• Setup and operate pharmaceutical production equipment including high-speed filling lines for sterile products, autoclaves, parts and vial washers, depyrogenation tunnel, formulation process, HMI, and automatic CIP/SIP processes, as well as inspection and packaging line equipment (e.g., AVIM, labeling, and carton machines) as per relevant SOPs and Batch Record.
• Responsible for formulation activities of production batches, including formulation and/or dispensing of drug substances and excipients.
• Responsible for parts preparation, washing, and sterilization of materials.
• Responsible for packaging and transfer of the final product to the freezer.
• Complete all relevant training before performing any task.
• Follow aseptic techniques and practices for aseptic operations.
• Carry out cleaning and upkeep of production equipment and classified manufacturing areas.
• Timely complete batch records and logbooks, adhering to GDP.
• Transfer materials for manufacturing a batch.
• Prepare filters for test execution and perform filter integrity testing (FIT).
• Provide for loading/unloading of loads/batches during production activities.
• Perform stock checks of consumables and inform managers of required materials.
• Follow safety and quality compliance at all times and report anomalies promptly.
• Participate in EHS, Business Compliance, cGMP, and other compliance-related matters.
• Perform all tasks according to SOPs and maintain strict GMP compliance, reporting quality issues immediately.
• Perform visual inspection, labeling, and packaging of finished drug products, and conduct in-process sampling and inspections.
• Perform any other duties as assigned by the Manager.

  Education

  • Minimum "O" Level, NITEC/ITE education, or Diploma in relevant field.