or apply directly on Forge Biologics's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 33 days Forge Biologics's roles stay open a median of 33 days
- Reposted
- No
- Salary listed
- No 0% of Forge Biologics's roles list one
- Ghost-job risk at Forge Biologics
- moderate 5 stale, 1 reposted of 21 open
- Hiring momentum
- 27 roles opened in the last 90 days ↑ up vs. the prior 90 days
- Last confirmed on the employer's board
- 2026-09-17
Measured from postings appearing on and disappearing from Forge Biologics's own greenhouse board since 2026-08-03. Full hiring picture for Forge Biologics.
About this role
The Specialist I, QA Operations at Forge Biologics is responsible for ensuring compliance with regulatory requirements and maintaining quality standards in AAV gene therapy manufacturing. Daily activities include overseeing operations in a cleanroom environment, performing batch record reviews, training manufacturing personnel on quality topics, and collaborating with cross-functional teams to support continuous process improvements. The role also involves preparing for audits and maintaining documentation control processes.
- benefits
- 5/5
- freshness
- 3/5
- career value
- 4/5
- role clarity
- 4/5
- pay transparency
- 0/5
Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of Forge Biologics as an employer.
What you need
- 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
- Ability to collaborate with cross-functional technical groups
- Strong communication skills
- Ability to work necessary hours to support production and participate in an on-call rotation
Nice to have
- Direct experience in providing QA support for cGMP manufacturing operations in a cleanroom environment
- Experience working in the production of biologics (ex. gene therapies)
- Knowledge 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
What you get
- Health, dental and vision insurance starting day one with 90% of premiums covered
- Competitive paid time off plan
- 12 weeks of fully paid parental leave
- Annual bonus opportunities for full-time team members
- 401(k) with company match
- Special employee discounts, including childcare and dependent care savings
Worth weighing
- The role requires working in a cleanroom environment and wearing PPE, which may not be suitable for everyone.
- The job involves participation in an on-call rotation, which may affect work-life balance.
Summarised from Forge Biologics's posting. Read the full original.
Listed by Forge Biologics on their greenhouse job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.
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