Night Shift Biotech Manufacturing Associate

CSL Vifor; Holly Springs (NC); On-site; USD 42,000 - 54,000; Full time

Job summary

CSL Vifor in Holly Springs, NC is seeking a dedicated shop floor operator for the night shift to manufacture high-quality biologics in a compliant, cost-effective manner. You will be trained on basic processes and equipment, performing sterile production tasks and supporting QA activities in a fast-paced biotech environment.

Responsibilities include cleaning, assembling, setting up and disassembly of equipment, following SOPs/BPRs, documenting activities, and interfacing with process automation

Qualifications

• High school diploma or GED or associate’s degree with 1+ years’ transferable skills, or bachelor’s with 0+ years’ experience, or equivalent.
• Experience in pharmaceutical/biotech/sterile production environments preferred.
• Basic knowledge of cGMP requirements preferred.
• Experience executing SOPs and documenting work preferred.

Responsibilities

• Becomes trained on basic processes and equipment and serves as a hands-on resource in Production.
• Conducts all assigned activities in a safe and cGMP compliant manner. Tasks include cleaning, preparing, and sterilizing production equipment; disinfecting rooms; assembly and disassembly of equipment; executing process steps per SOPs/BPRs; documenting activities; handling hazardous materials.
• Interface with process automation systems and electronic business systems (e.g., PAS, BAS, PLCs, LIMS, SAP)
• Support Qualification and Validation activities and document issues; assist CAPA investigations.
• Support team effort in root cause investigations and maintain a high-performance teamwork environment.

Skills

Mechanical aptitude

cGMP awareness

SOP execution

Education

High School Diploma or GED

Associate's degree or higher

Job description

CSL Vifor in Holly Springs, NC is seeking a dedicated shop floor operator for the night shift to manufacture high-quality biologics in a compliant, cost-effective manner. You will be trained on basic processes and equipment, performing sterile production tasks and supporting QA activities in a fast-paced biotech environment.

Responsibilities include cleaning, assembling, setting up and disassembly of equipment, following SOPs/BPRs, documenting activities, and interfacing with process automation