Formulation Technician II

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profile Job Location:

Singapore - Singapore

profile Monthly Salary: Not Disclosed
Posted on: 30+ days ago
Vacancies: 1 Vacancy

Job Summary

Work Schedule

Flex 12 hr shift/nights

Environmental 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.) Will work with hazardous/toxic materials

Job Description

Join Thermo Fisher Scientific and contribute to important impactful work. As a Formulation Technician II youll have the opportunity to work with world-class colleagues and use outstanding resources that our global leadership provides. Be part of our ambitious team where you can successfully apply strategies that make a difference!

Responsibilities

  • Setup and operate pharmaceutical production equipment including high-speed filling lines for sterile products autoclave 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 machine) according to relevant SOPs and Batch Records.
  • Manage formulation activities of production batches including formulation and/or dispensing of all available drug substances and excipients.
  • Prepare wash and sterilize materials and parts.
  • Package and transfer final product to the freezer.
  • Complete all relevant training before performing any task.
  • Strictly adhere to aseptic techniques and practices for aseptic operations.
  • Clean and maintain production equipment and classified areas in the manufacturing area.
  • Complete relevant batch records and logbooks on time adhering to GDP (Good Documentation Practice).
  • Transfer materials for batch manufacturing.
  • Prepare filters for test execution and perform FIT (filter integrity testing).
  • Load and unload batches from equipment during production activities.
  • Perform stock checks of consumables and inform Manager/Lead Technician of required materials.
  • Adhere to safety and quality standards consistently and promptly inform the manager of any irregularities.
  • Participate in EHS Business Compliance cGMP and other compliance-related matters.
  • Carry out all duties following SOPs and adhere to strict GMP standards consistently. Promptly notify the Manager or Lead Technician of any quality concerns.
  • Conduct visual inspections labeling and packaging of finished drug products. Perform in-process sampling on semi-finished drug products and conduct in-process inspections.

Education

  • Minimum O Level NITEC/ITE education/Diploma in a relevant field.

Experience

  • 1 to 2 years of valuable experience in the pharmaceutical sector or 3 to 5 years of professional experience in any field.

Knowledge Skills Abilities

  • Good understanding of safe working practices and cGMP.
  • Eager to contribute in the pharmaceutical sector.
  • Capable of collaborating effectively within a team environment.
  • Capable of handling rotating shifts.


Required Experience:

IC

Work ScheduleFlex 12 hr shift/nightsEnvironmental ConditionsAble 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 -22d...
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Electron microscopes reveal hidden wonders that are smaller than the human eye can see. They fire electrons and create images, magnifying micrometer and nanometer structures by up to ten million times, providing a spectacular level of detail, even allowing researchers to view single a ... View more

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