Specialist I, QA Operations (2nd Shift)

Forge Biologics; Columbus (OH); On-site; USD 75,000 - 105,000; Full time

Job summary

Forge Biologics is seeking a Specialist I, QA Operations (AAV Manufacturing) to ensure regulatory compliance and uphold high quality standards in our GMP cleanroom environment. You will support document control, batch record reviews, and maintain a QA presence across AAV gene therapy manufacturing areas.

The role requires collaboration with Process Development, Analytical Development, and Manufacturing teams, along with deviations and CAPA activities, audits, and continual process improvements.

Qualifications

• Bachelor’s degree in a scientific or related field (or equivalent experience).
• Experience in a quality assurance role within pharma/biotech.
• Keen attention to detail with accurate documentation across tasks.
• Ability to collaborate with cross-functional technical groups to resolve issues.
• Strong communication skills to convey quality issues to leadership.
• Willingness to work production hours and participate in on-call rotation.
• Ability to work in a GMP cleanroom environment with appropriate PPE.

Responsibilities

• Serve as a quality resource for GMP AAV manufacturing, guiding management on quality issues in the cleanroom.

Skills

Attention to detail

Cross-functional collaboration

Quality issues communication

GMP compliance

Documentation accuracy

On-call readiness

Cleanroom operations

Education

Bachelor’s degree in science or related field

Tools

eQMS (Veeva Vault)

Microsoft Office (Outlook/Teams/Word/Excel/PowerPoint)

Job description

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 arehardworking, showing up each day with determination and grit. We areopen, creating a space where ideas flow freely, and every voice is valued. We arepurpose-driven, with every task directly tied to changing lives. And we areengaged, 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:

We are currently seeking a Specialist I, QA Operations (AAV Manufacturing) to join the Forge Biologics Team. The Specialist I, QA Operations is responsible for ensuring compliance with regulatory requirements and maintaining the highest quality standards. Th is role will support the Quality Assurance team in activities such as document control, batch record review, and helping maintain a QA presence in AAV gene therapy manufacturing areas.

Responsibilities:

• Serves as a quality resource for the GMP AAV Manufacturing department directly overseeing operations in the cleanroom manufacturing environment, providing guidance and effectively communicat ing to management Quality issues that arise during the manufacturing of product.
• Perform detailed review and approval of batch records and associated documentation for AAV gene therapy manufacturing, logbooks, and other controlled documentation ensuring adherence to established procedures and cGMP regulations.
• Provide training and guidance to manufacturing personnel on quality-related topics, ensuring proper understanding and adherence to AAV gene therapy manufacturing procedures and regulatory requirements.
• S upport deviations and continuous improvements related to AAV gene therapy manufacturing processes, assist with root cause analysis and identification of CAPA measures to prevent recurrence.
• Collaborate with cross-functional teams, including Process Development, Analytical Development, and Manufacturing, to support continuous process improvement initiatives and ensure alignment with quality objectives .
• Support the documentation control process for AAV gene therapy manufacturing, including reviewing and revising SOPs, work instructions, and forms to ensure compliance with regulatory requirements and industry best practices.
• Assist in the preparation for external audits and inspections, supporting regulatory agencies or client audits specific to AAV gene therapy manufacturing.

Qualifications:

• Bachelor’s Degree in a scientific or related field (or equivalent experience).
• Previous experience in a quality assurance role within the pharmaceutical or biotechnology industry.
• Proven track record of keen attention to detail, consistently ensuring accuracy and precision in all tasks and documentation, managing multiple priorities in a fast-paced environment
• Ability to collaborate with cross-functional technical groups to resolve issues, close gaps, and ensure compliant outcomes which are efficient and robust.
• Strong communication skills, including the ability to effectively communicate quality issues to senior management.
• Ability to work the hours necessary to support production and participate in an on-call rotation providing off-hours support for AAV manufacturing needs and issues .
• Ability to work in a GMP cleanroom environment as needed to support manufacturing operations, which includes wearing required PPE such as gowns, gloves, masks, and safety glasses.

Preferred Skills:

• Direct experience in providing QA support for cGMP manufacturing operations in a cleanroom environment .
• Experience working in the production of biologics (ex. gene therapies).
• K nowledge of cGMP regulations, quality systems, and quality assurance principles .
• Experience utilizing an eQMS , preferably Veeva Vault or another document management system.
• Intermediate proficiency in Microsoft Office applications (Outlook, Teams, Word, Excel, and PowerPoint ).
• Experience supporting internal audits and participating in external audits or inspections .

This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities and activities may change, or new ones may be assigned.

Work Environment and Physical Demands

This position is performed in a temperature-controlled laboratory or office environment and requires regular standing, hand manipulation, and use of laboratory equipment. The role may involve lifting or moving materials up to 25 pounds and occasional reaching or handling at various heights. Appropriate personal protective equipment (PPE) must be worn when working with chemicals, biological materials, or in controlled environments.

Forge Biologics is an equal opportunity employer dedicated to building an inclusive and diverse workforce. Forge Biologics, provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

At Forge Biologics, we believe our people deserve to be taken care of – in and out of the workplace. We’ve built a comprehensive compensation and benefits package designed to help you thrive, grow, and feel valued every step of the way:

Health from day one

• Health, dental and vision insurance start your first day – with 90% of premiums covered for youandyour family.

Time to recharge

• A competitive paid time off plan – because rest fuels innovation.
• 12 weeks of fully paid parental leave so you can focus on family when it matters most.

Rewarding your impact

• Annual bonus opportunities for all full-time team members.
• 401(k) with company match to help you plan for the future.
• Special employee discounts, including childcare and dependent care savings.
• Onsite fitness facility at The Hearth.
• Mental health counseling and financial planning services through our Employee Assistance Program.
• Employer-paid short and long-term disability coverage to protect your peace of mind.

Fuel for your workday

• A fully stocked kitchen with free snacks and beverages – we keep you energized and ready for what’s next.

Grow with us

• Ongoing professional development resources, training, and mentorship programs to help you build your care and grow within Forge.