Operator II, Mfg (12hr nights or 12hr days, 2-2-3 rotation)

Thermo Fisher Scientific•Greenville, NC

12d•Onsite

About The Position

Job Description COMPANY INFORMATION As part of the Thermo Fisher Scientific team, you’ll 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 world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. GROUP/DIVISION SUMMARY 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. S hift hours are 6am-6pm or 6pm-6am on a 2-2-3 rotating schedule. POSITION SUMMARY 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.

Requirements

HS Diploma or equivalent minimally required.
1-2 years of work experience in manufacturing/production, operations, lab setting; pharma preferred.
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.

Nice To Haves

Equivalent combinations of education, training, and relevant work experience may be considered.

Responsibilities

Ensures 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 tray loaders.
Filter integrity testing.
Clean pre and post use change parts and prep for sterilization.
Maintain/clean classified and non-classified areas. This includes but is not limited to the aseptic core.
Record and complete accurate documentation according to GMP requirements.
Drive a culture of safety and quality in all activities.
Perform visual inspections on in-process and finished products and call out inconsistencies when appropriate.
Work with a team in a fast-paced environment assembling product.