Sterile Injectables Manufacturing Tech II

Alcami; Morrisville (NC); On-site; USD 34,000 - 44,000; Full time

Job summary

Alcami is seeking a Manufacturing Technician II (Compound/Fill/Finish) to join our on-site team in a fast-paced sterile liquid manufacturing environment. You will operate aseptic equipment, perform compounding and filling, and maintain strict cGMP documentation and quality standards.

Responsibilities include equipment setup, process execution, in-process sampling, and ensuring product quality while adhering to SOPs and batch records.

Qualifications

• High school diploma or GED required; associate or bachelor’s degree preferred.
• 1–2 years of work experience required; 2–5 years preferred.
• Prior experience in a cGMP pharmaceutical manufacturing environment required.
• Experience in dispensing, compounding, aseptic filling, or visual inspection is highly desirable.
• Life sciences or engineering degrees considered without manufacturing experience.

Responsibilities

• Learns and executes manufacturing operations, including setup, operation, and maintenance of equipment used in dispensing, compounding, filling (isolators), and visual inspection.
• Becomes a subject matter expert on compounding and filling processes and equipment.
• Performs production processes with adherence to SOPs, batch records, quality standards, and minimal deviations to maintain product quality.
• Conducts in-process and end-of-process sampling/quality checks to ensure product quality.
• Identifies inefficiencies and escalates to supervision to support continuous process improvement.
• Maintains accurate and detailed production documentation with minimal errors and recommends revisions to reduce errors.

Skills

Communication

Teamwork

Troubleshooting

Math skills

Documentation

GMP knowledge

Safety awareness

Independent work

Education

High school diploma or GED

Associate degree preferred

Bachelor’s degree preferred

Job description

Alcami is seeking a Manufacturing Technician II (Compound/Fill/Finish) to join our on-site team in a fast-paced sterile liquid manufacturing environment. You will operate aseptic equipment, perform compounding and filling, and maintain strict cGMP documentation and quality standards.

Responsibilities include equipment setup, process execution, in-process sampling, and ensuring product quality while adhering to SOPs and batch records.