Pharma Manufacturing Technician III - On-Site Day Shift

Alcami Corporation

Wilmington (NC)

On-site

USD 55,000 - 75,000

Full time

14 days+
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Job summary

Alcami Corporation is seeking a Manufacturing Technician III OSD to support on-site production of oral solid dosage products. You will follow SOPs, operate processing equipment, and document activities in real time while complying with cGMP and FDA regulations.

The role requires 4–6+ years of relevant pharmaceutical manufacturing experience, a high school diploma or GED (associate degree preferred), and willingness to work a 1st shift Monday–Thursday 6:30am–5:00pm with possible weekend work.

Qualifications

  • High school diploma or GED is required; Associate degree preferred.
  • 4–6+ years of relevant experience preferred.
  • Experience in drug substance manufacturing and cGMP environment preferred.

Responsibilities

  • Follow SOPs and cGMPs to perform duties.
  • Ensure timely completion and compliance with training requirements.
  • Operate manufacturing techniques and equipment per SOPs and cGMPs.
  • Document activities in real time on controlled documentation per SOPs and cGMPs.
  • Perform in-process testing, weight checks, component counting and basic math calculations.
  • Assist with other manufacturing areas as required.
  • Perform production tasks in Solid Oral Dosage: Microencapsulation, Blending, and Bulk Packaging.
  • Maintain accurate production documentation in compliance with GMP and FDA regulations.
  • Work occasional hours outside scheduled shift, including weekends, as needed.

Skills

Verbal communication
Written communication
Documentation
Attention to detail
Problem-solving
Reading instructions
Math calculations
PPE proficiency

Education

High school diploma or GED
Associate's degree preferred

Job description

Alcami Corporation is seeking a Manufacturing Technician III OSD to support on-site production of oral solid dosage products. You will follow SOPs, operate processing equipment, and document activities in real time while complying with cGMP and FDA regulations.

The role requires 4–6+ years of relevant pharmaceutical manufacturing experience, a high school diploma or GED (associate degree preferred), and willingness to work a 1st shift Monday–Thursday 6:30am–5:00pm with possible weekend work.

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