GMP Formulation & Filling Technician

Augustbioservices; United States; On-site; USD 40,000 - 54,000; Full time

Job summary

August Bioservices, headquartered in Nashville, TN, is hiring experienced manufacturing technicians to support formulations and filling teams. The role requires a High School diploma or equivalent, with 1+ year in pharmaceutical manufacturing and GMP/GDP understanding.

You will operate equipment, perform cleaning, manage materials, and document activities per batch records. Join a growing CDMO focused on drug discovery, formulation, and manufacturing, collaborating with QA, QC, engineering, and

Qualifications

• High School Diploma or equivalent required.
• Associate degree in a technical field or a bachelor's in biological, chemical sciences, or engineering preferred but not required.
• 1+ years in pharmaceutical manufacturing environments.
• Familiarity with GMP and GDP standards.
• Strong attention to detail and ability to follow SOPs.

Responsibilities

• Perform routine cleaning and sanitization of production areas to maintain a controlled environment.
• Prepare and transfer materials for production using proper aseptic handling techniques.
• Operate and maintain equipment used across production processes (formulation, filling, sterilization, packaging).
• Complete GMP documentation, batch records, protocols, and deviations per GDP.
• Collaborate with production, QA, QC, engineering, validation, and maintenance teams as required.
• Recognize and report deviations or equipment malfunctions to management.

Skills

Mechanical aptitude

Attention to detail

Documentation skills

Verbal and written communication

Team collaboration

Education

High School Diploma or equivalent

Technical associate or Bachelor’s preferred but not required

Job description

August Bioservices, headquartered in Nashville, TN, is hiring experienced manufacturing technicians to support formulations and filling teams. The role requires a High School diploma or equivalent, with 1+ year in pharmaceutical manufacturing and GMP/GDP understanding.

You will operate equipment, perform cleaning, manage materials, and document activities per batch records. Join a growing CDMO focused on drug discovery, formulation, and manufacturing, collaborating with QA, QC, engineering, and