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Technician I, GMP Manufacturing Support - Sanitization (1st Shift

Job in Columbus, Franklin County, Ohio, 43224, USA
Listing for: Forge Biologics
Full Time position
Listed on 2026-07-31
Job specializations:
  • Manufacturing / Production
    Manufacturing & Industrial Operations, Pharmaceutical Manufacturing
Salary/Wage Range or Industry Benchmark: 36000 - 60000 USD Yearly USD 36000.00 60000.00 YEAR
Job Description & How to Apply Below
Position: Technician I, GMP Manufacturing Support - Sanitization (1st Shift)

At Forge Biologics, we believe in turning bold ideas into life-changing realities. Our mission is simple yet powerful: to enable access to life-changing gene therapies and help bring them from ideas into reality. We partner with scientists, physicians, biotech and pharma innovators, and patient communities — all united by one goal: improving lives. If you’re driven by purpose and excited to make a tangible impact, this is where your journey begins.

Our team works out of The Hearth, a state-of-the-art, 200,000-square-foot cGMP facility in Columbus, Ohio. Here, you won’t just watch innovation happen — you’ll be part of it. Whether you’re scaling AAV manufacturing, collaborating on cutting-edge therapies, or supporting complex technical projects, you’ll play a key role in bringing hope to patients with genetic diseases.

What sets Forge apart is our culture ofH.O.P.E.We are
hardworking
, showing up each day with determination and grit. We are
open
, creating a space where ideas flow freely, and every voice is valued. We are
purpose-driven
, with every task directly tied to changing lives. And we are
engaged
, energized by the challenges we face and the milestones we achieve together.

At Forge, your growth matters. We’re committed to helping you expand your skills, take on new challenges, and develop your career through mentorship, hands-on learning, and opportunities for advancement. Our people are our greatest investment, and we’re proud to see team members grow with us.

If you’re ready to use your talent to help deliver hope to patients around the world, join us — and be part of something bigger than yourself.

About The Role:

The Technician I, GMP Manufacturing Support , performs a wide range of functions crucial to AAV gene therapy production. This position is responsible for cleaning and sanitization of GMP equipment and facilities, preparing tubing sets and inventory management within the cleanroom space. This entry-level position offers an opportunity to gain foundational experience in the multifaceted support activities crucial for the production of AAV gene therapy products.

Responsibilities:
  • Perform the cleaning and sanitization of GMP manufacturing facilities and equipment, ensuring compliance with SOPs and cGMPregulations.
  • Assistin tube set preparation under supervision, adhering to specific procedures and documentation practices.
  • Replenish cleaning andconsumablessuppliesrequiredfor manufacturing operations, setting reorder points, and placing orders as per forecastdemand.
  • Stock andmaintaincommon-use items in the cleanroom, ensuring that inventory levels are adequate for daily operations and that items are readily available.
  • Monitor theexpirationdates and conditions of consumables, ensuring that they are rotated and replaced as necessary to prevent shortages or non-compliance.
  • Maintain real-time andaccuratedocumentation; perform the manufacturing review of logbooks, MPR’s, and associated documents.
  • Assistin troubleshooting and resolving minor equipment or process-related issues under the guidance of senior team members.
  • Collaborate with cross-functional teams, including GMP Manufacturing, Quality Assurance, Quality Control, and Product Development, to support efficient manufacturing operations.
  • Assistin equipment setup, inventory management, and material requests for cleaning and manufacturing activities.
  • Contribute to process improvement initiatives, providing feedback and suggestions to enhance department-related processes and improve efficiency.
  • Follow safety procedures andmaintaina clean workspace.
Qualifications:
  • High school diploma or equivalentGEDrequired
  • 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 Personal Protective Equipment (PPE) as needed
Preferred

Skills:
  • Prior experience in a manufacturing or laboratory environment.
  • Exposure to facility or equipment cleaning and sanitization or equipment building and setup.

This job description is not designed to cover or contain a…

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