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...
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
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