Packaging/Labeling Technician II (10hr 1st shift; Tues-Fri)
About The Position
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. 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! How Will You Make an Impact?: Sets-up, operates, and maintains the classified environments and manufacturing equipment for pharmaceutical products. Requires proficiency in; cleaning, preparing equipment and components for operations, operating and troubleshooting mechanical equipment, following approved procedures and proper documentation. Position is a 10-hour first shift (Tuesday-Friday)
Requirements
- High school diploma or equivalent required.
- Minimum of 1 year of work experience in a manufacturing, operations, production, lab setting or related field
- 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.
Nice To Haves
- Experience in a cGMP environment
Responsibilities
- Ensures operations are performed in a safe and responsible manner striving to create an injury-free and incident-free workplace.
- Ensures pharmaceutical products in manufacturing are in accordance to Standard Operating Procedures (SOPs) and Current Good Manufacturing Practices (cGMPs) and other batch related activities.
- Verifies and documents production activities in batch records, logbooks, etc.
- Assists in troubleshooting operational and production problems in order to identify appropriate corrective actions.
- Maintains/cleans classified environments/areas.
- Communicates and works to resolve any production, quality or safety issues.
- Complies with all job-related safety, cGMP, and other department procedural requirements.
- Participates in the On the Job (OJT) training program, area safety initiatives, and area lean manufacturing initiatives.
- Perform other related duties as required by the job or directed by the supervisor.
- Trains new employees.
- Performs other duties as assigned
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED
