Operator I Steriles East (12hr nights, D shift, 2-2-3)

at  Thermo Fisher Scientific

JOB DESCRIPTION

As part of the Drug Product Division (DPD), the Greenville, North Carolina site is a multi-purpose pharmaceutical development, manufacturing, and packaging campus. The operation specializes in taking both sterile injectable and oral solid dose drug products from development phase through to commercialization!

EDUCATION

• High school diploma or equivalent is minimally required.

EXPERIENCE

• Some pharmaceutical production experience preferred (0-1 years)
• Preferred: Experience in a cGMP environment

KNOWLEDGE, SKILLS, ABILITIES

• Excels in a team environment.
• Basic math skills.
• Good verbal/written communication.
• Attention to detail while maintaining a quality product.
• Ability to perform repetitive work duties.
• Ability to follow SOPs.

PHYSICAL REQUIREMENTS/WORK ENVIRONMENT

• Work in a clean-room which is a controlled environment for temperature and humidity having low ambient noise.
• Wear gowning which includes: gloves, hair & beard net and face cover, safety glasses with no makeup / jewelry, and the like.
• Use Personal Protective Equipment (PPE) and understand chemical hygiene.
• Infrequently lift and manipulate up to 25 pounds max unassisted.
• Stand and move about including reaching, bending, stooping, grasping.
• Use hand tools and equipment including forceful gripping, grasping, pushing and pulling.
• Job requires basic mobility and coordination to navigate office areas; ability to stand, walk, bend, and carry light to medium objects (10-35 pounds).
  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

• 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 trayloader
• Filter integrity testing
• Clean pre and post use change parts and prep for sterilization.
• Component/commodity prep.
• General material handling
• Maintain/clean classified and non-classified areas. This includes but is not limited to the aseptic core.
• In-process product inspection
• Participate in the On the Job (OJT) training program, area safety and Lean Manufacturing initiatives.
• Perform other activities as required.