Greenville Operator I Grads To Work Program (12hr days or 12hr nights)
Greenville Operator I Grads To Work Program (12hr days or 12hr nights)
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1 Vacancy
Job Description
Work Schedule
12 hr shift/daysEnvironmental 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 Some degree of PPE (Personal Protective Equipment) required (safety glasses gowning gloves lab coat ear plugs etc.) Strong Odors (chemical lubricants biological products etc.)Job Description
Greenville Operator I Grads To Work Program (Certification Required)
As part of the Thermo Fisher Scientific team youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the worlds toughest challenges like protecting the environment making sure our food is safe or helping find cures for cancer. Shift hours are 6am-6pm or 6pm-6am on a 2-2-3 rotating schedule.
Location/Division Specific Information
Greenville NC
How will you make an impact
The Manufacturing Operator will be responsible for the manufacturing equipment for filling pharmaceutical products in a clean room environment. They will carry out the production process by closely following the Standard Operating Procedures (SOP) and Work Instruction Documents as they relate to assembly materials handling equipment operation and finished products.
What will you do
- Ensure pharmaceutical products are manufactured in accordance with area SOPs and current cGMP.
- Verify and document production activities in batch records logbooks and controlled forms.
- Operate vial trayloader
- Conduct filter integrity testing
- Clean pre and post-use change parts and prepare them for sterilization.
- Prepare components/commodities.
- Handle general materials.
- Maintain/clean classified and non-classified areas including the aseptic core.
- Inspect in-process products.
- Participate in the On the Job (OJT) training program area safety and Lean Manufacturing initiatives.
- Perform other activities as the need arises.
How will you get here
Education
- High school diploma or equivalent minimally required.
Experience
- Preferred: 0-1 year of regulated manufacturing experience preferably Pharmaceutical experience.
Equivalency:
- Equivalent combinations of education training and relevant work experience may be considered.
Knowledge Skills Abilities
- Ensure pharmaceutical products are manufactured in accordance to area SOPs and current cGMP.
- Verify and document production activities in batch records logbooks and controlled forms.
- Operate vial tray loader.
- Filter integrity testing.
- Clean pre and post use change parts and prep for sterilization.
- In-process product inspection.
- Participate in on the Job (OJT) training program area safety and Lean Manufacturing initiatives.
- General material handling.
- Maintain/clean classified and non-classified areas. This includes but is not limited to aseptic core.
- Component/commodity prep.
Employment Type
Full-Time
