Formulation Technician II

at  Thermo Fisher Scientific

Greenville, NC 27834, USA -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate24 Dec, 2024Not Specified25 Sep, 20242 year(s) or aboveColor,Motion,Sterilization,Mechanical Troubleshooting,Documentation PracticesNoNo
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Description:

JOB DESCRIPTION

When you’re part of the team at Thermo Fisher Scientific, you’ll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you’ll be supported in achieving your career goals.

REQUIREMENTS

High school diploma or equivalent required. Technical degree preferred.
2 years of supervised manufacturing (Pharmaceutical preferred), mechanical or similar experience.

KNOWLEDGE, SKILLS, ABILITIES

  • General mechanical, electrical, pneumatic and hydraulic knowledge.
  • Mechanical troubleshooting (manufacturing equipment preferred)
  • Aseptic Cleaning
  • Equipment change part cleaning and sterilization
  • Component/commodity sterilization
  • Aseptic gowning/technique
  • Good documentation practices
  • Good written and verbal communication
  • Ability to use a computer
  • Ability and desire to learn
  • Stand for long periods of time
  • Ability to work with cross-functional teams comprised of diverse individuals.
  • Ability to manipulate (lift, carry, move) weights of 25-50 pounds; occasionally pushing and pulling 50-100+ pounds.
  • Full range of motion in upper and lower extremities.
    At Thermo Fisher Scientific, each one of our 70,000 extraordinary minds has a unique story to tell. Join us and give to our singular mission—enabling our customers to make the world healthier, cleaner and safer.
    Apply today! http://jobs.thermofisher.com
    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.
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Responsibilities:

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:
Filler
Capper
Freeze dryer (Lyo) loading/Unloading
Trayloader
Vial Washer
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.
Mechanical troubleshooting
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.


REQUIREMENT SUMMARY

Min:2.0Max:7.0 year(s)

Mechanical or Industrial Engineering

Engineering Design / R&D

Mechanical Engineering

Diploma

Proficient

1

Greenville, NC 27834, USA