GMP Buffers Technician I — 3rd Shift (Entry Level)

Forge Biologics; Columbus (OH); On-site; USD 25,000 - 36,000; Full time

Benefits offered by this job

Health insurance

Paid time off

Parental leave

Annual bonus

Job summary

Forge Biologics in Columbus, Ohio is seeking a Technician I, GMP Support – Buffers to contribute to buffer and media formulation for AAV gene therapy production. This entry-level role offers hands-on exposure to cGMP environments and cross-functional collaboration.

You will follow SOPs, maintain accurate documentation, assist with equipment setup, and support quality, manufacturing, and product development teams while adhering to strict GMP gowning and safety protocols.

Qualifications

• High school diploma or equivalent.
• Experience following SOPs or other protocols/work instructions.
• Basic computer skills and the ability to learn and use manufacturing software.
• Ability to work the hours necessary to support production and/or product transfer activities.
• Ability to work in loud noise environments and in PPE as needed.
• Ability to work a 3rd shift: 4 x 10-hour schedule (Sun night–Thu morning).

Responsibilities

• Assist in media and buffer preparation under supervision, adhering to schedules and SOPs.
• Maintain real-time and accurate documentation; review logbooks and associated documents.
• Assist in troubleshooting and resolving minor equipment or process-related issues.
• Collaborate with GMP Manufacturing, QA, QC, and Product Development teams.
• Assist in equipment setup, inventory management, and material requests for cleaning and manufacturing.
• Follow GMP gowning procedures and safety protocols in cleanroom environments.
• Contribute to process-improvement initiatives and efficiency efforts.
• Maintain a clean workspace and adhere to safety procedures.

Skills

SOP adherence

Quality documentation

Teamwork

GMP awareness

Education

High school diploma

Tools

PC literacy

Job description

Forge Biologics in Columbus, Ohio is seeking a Technician I, GMP Support – Buffers to contribute to buffer and media formulation for AAV gene therapy production. This entry-level role offers hands-on exposure to cGMP environments and cross-functional collaboration.

You will follow SOPs, maintain accurate documentation, assist with equipment setup, and support quality, manufacturing, and product development teams while adhering to strict GMP gowning and safety protocols.