This list contains only the countries for which job offers have been published in the selected language (e.g., in the French version, only job offers written in French are displayed, and in the English version, only those in English).
Prepare the clean room (materials, resources, prescriptions, etc.) with the aim of eliminating any errors and to work according to Good Manufacturing Practices. Maintains a sterile environment in the clean room, by garbing, cleaning the room, and behaving according to cleanroom procedures that align with CGMP practices or guidelines. Prepares and sterilizes components/vials for appropriate solutions; sterilizes solutions and fills into specified containers. Prepare individual pharmaceutical compounds according to schedule and prescribed medication as well as GMP requirements, with the aim of providing the patient with the correct medication. Check prescriptions and compound preparations (personal details, dosing, validity date, etc.) and label and send the medication out, with the aim of ensuring that the patient is provided with the correct medication. According to defined guidelines, clean the equipment and the workplace as well as monitor possible residual materials with the aim of working in a neat and clean environment which adheres to the quality guidelines so as to prevent accidents and incidents. Show respect for the quality, neatness and safety guidelines when carrying out production orders with the aim of preventing accidents and other unwanted incidents. Clock in and out for every scheduled shift in a timely manner. Other duties as assigned. Collection of vials out of cleanroom pass throughs, ensuring stoppers are set flush in vials per SOP. Labels are placed on trays, label and Lot control. Working within the team on first in and first out rotation of crimping. Tracking batches within Felton per SOP. Equipment prep and maintenance. Autoclaving and ensuring proper sterilization occurred on batches required. Proper documentation.
Job Responsibility:
Prepare the clean room (materials, resources, prescriptions, etc.) with the aim of eliminating any errors and to work according to Good Manufacturing Practices
Maintains a sterile environment in the clean room, by garbing, cleaning the room, and behaving according to cleanroom procedures that align with CGMP practices or guidelines
Prepares and sterilizes components/vials for appropriate solutions
sterilizes solutions and fills into specified containers
Prepare individual pharmaceutical compounds according to schedule and prescribed medication as well as GMP requirements, with the aim of providing the patient with the correct medication
Check prescriptions and compound preparations (personal details, dosing, validity date, etc.) and label and send the medication out, with the aim of ensuring that the patient is provided with the correct medication
According to defined guidelines, clean the equipment and the workplace as well as monitor possible residual materials with the aim of working in a neat and clean environment which adheres to the quality guidelines so as to prevent accidents and incidents
Show respect for the quality, neatness and safety guidelines when carrying out production orders with the aim of preventing accidents and other unwanted incidents
Clock in and out for every scheduled shift in a timely manner
Other duties as assigned
Collection of vials out of cleanroom pass throughs, ensuring stoppers are set flush in vials per SOP
Labels are placed on trays, label and Lot control
Working within the team on first in and first out rotation of crimping
Tracking batches within Felton per SOP
Equipment prep and maintenance
Autoclaving and ensuring proper sterilization occurred on batches required
Proper documentation
Requirements:
Experience working in a production environment, ideally in a cleanroom setting
Ability to effectively communicate with others
Ability to lift up to 60 lbs
High school diploma or equivalent
one to four years previous work experience in a hospital or manufacturing environment or doing aseptic filling
Knowledge of clean room procedures, preferred but not required
Knowledge of and compliance with CGMP (Current Good Manufacturing Practices) regulations, preferred but not required
Ability to take initiative, including asking for and offering help when needed
performs work independently without being prompted
Ability to prioritize and plan work activities. Manages time effectively and adapts quickly to changing priorities
Ability to work within tight timelines
Ability to handle multiple tasks and organize resources to ensure work is completed on time
Strong attention to detail and focus on quality, accuracy, sterility, and aseptic technique
Basic computer and math skills
Positive attitude and the ability to work in a team environment
Nice to have:
Knowledge of clean room procedures
Knowledge of and compliance with CGMP (Current Good Manufacturing Practices) regulations
What we offer:
competitive salary
comprehensive benefits
performance package
ability to be part of an international leader in an expanding industry