How will you make an impact?
Sets-up, operate, and maintain classified environments along with manufacturing equipment for filling pharmaceutical products.
What will you do?
Ensures pharmaceutical products are manufactured in accordance to area SOPs and current cGMP.
Verify and document production activities in batch records, logbooks and controlled forms.
Complete assembly, disassembly and operation of area manufacturing equipment inside/outside the aseptic core:
Freeze dryer (Lyo) loading/Unloading
SMEJA stopper processor
Equipment and component sterilizers
Filter integrity testers
Piping changeover’s on the product delivery systems and CIP/SIP cycles (Filler/Stopper isolator)
Assist with initial/subsequent validation of filling equipment and processes.
General material handling
Maintain/clean classified areas. This includes but is not limited to the aseptic core.
Clean pre and post use change parts and prep for sterilization.
Participate in the On the Job (OJT) training program, area safety and Lean Manufacturing initiatives.
Train new employees.
How will you get here?
High school diploma or equivalent required. Technical degree preferred.
2 years of regulated manufacturing (Pharmaceutical preferred), mechanical or similar experience.
Knowledge, Skills, Abilities
General mechanical, electrical, pneumatic and hydraulic knowledge.
Mechanical troubleshooting (manufacturing equipment preferred)
Equipment change part cleaning and sterilization
If you are an individual with a disability who requires reasonable accommodation to complete any part of our application process, click here for further assistance.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.