Filling Technician I, Nights
BioSpace
Clayton, NCFresher1h agovia LinkedIn
About the Role
Novo Nordisk's Product Supply Aseptic Manufacturing (PS AM) facility in Clayton, NC is a 457,000 square foot aseptic "fill and finish" site responsible for producing innovative, injectable diabetes and obesity treatments.
Key Responsibilities
- Filling of insulin & media preparations under aseptic conditions.
- Operation of inspection equipment to achieve production goals.
- Operate, monitor & control equipment, systems & processes associated with Vial/Cartridge filling.
- Achieve production goals.
- Maintain aseptic areas & perform sanitizations & environmental monitoring.
- Participate actively in & support event response.
- Review documents as required.
- Assist during equipment maintenance, including restoration of lost function, predictive & preventative maintenance.
- Record/review production data in BPR’s & associated forms.
- Follow all safety & environmental requirements.
Physical Requirements
- Moves equipment &/or supplies weighing up to 33 pounds.
- Routinely operates & inspects manufacturing equipment.
- Strap & unstrap pallets.
- Ability to be on your feet for up to a 12-hour shift.
- May require corrected vision to 20/20 or 20/25.
- May require colour vision.
- Occasionally ascends/descends a ladder.
- May be required to work at elevated heights.
- Occasionally works around odorous &/or hazardous materials.
- May be required to wear latex gloves.
- May perform critical job functions in extremely cold work environments.
- May position oneself within confined spaces for inspection.
- Ability to work in loud noise environments with hearing protection.
- May be required to secure a motorized vehicle license & operate a motorized vehicle.
Qualifications
- High School Diploma or equivalent.
- Minimum of six (6) months manufacturing experience (Requirement may be waived with military experience, a BioWorks/BioBlend certification or equivalent from an accredited college, or a current Novo Nordisk contractor with 3 months of demonstrated performance).
- Aseptic Processing Experience (Preferred).
- Experience working in an FDA regulated environment (Preferred).
- Ability to read, write & understand complicated product documentation & standard operating procedures with attention to detail.
- Computer literacy (Preferred).