or apply directly on Aspect Biosystems's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 102 days Aspect Biosystems's roles stay open a median of 91 days
- Reposted
- No
- Salary listed
- Yes 83% of Aspect Biosystems's roles list one
- Ghost-job risk at Aspect Biosystems
- high 12 stale, 1 reposted of 12 open
- Hiring momentum
- 6 roles opened in the last 90 days ↓ down vs. the prior 90 days
- Last confirmed on the employer's board
- 2026-11-14
Measured from postings appearing on and disappearing from Aspect Biosystems's own greenhouse board since 2026-08-03. Full hiring picture for Aspect Biosystems.
About this role
The Head of Quality Assurance at Aspect will lead the QA team and ensure GxP compliance for bioprinted tissue therapeutics. Responsibilities include establishing a GMP-compliant Quality Management System, overseeing core QA functions, leading inspection readiness activities, and collaborating on regulatory submissions. This role also involves building a high-performing QA team and engaging with regulatory agencies.
- benefits
- 2/5
- freshness
- 1/5
- career value
- 4/5
- role clarity
- 5/5
- pay transparency
- 5/5
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 Aspect Biosystems as an employer.
What you need
- Bachelor’s, Master’s, or Ph.D. in Life Sciences, Biotechnology, Chemistry, Engineering, or a related scientific discipline
- 10+ years of progressive Quality Assurance leadership experience within a GMP-regulated biotech, pharmaceutical, or advanced biologics environment
- Expert understanding and practical application of global regulatory guidelines (FDA, EMA, Health Canada, ICH)
- Demonstrated success in establishing, scaling, and maintaining a phase-appropriate Quality Management System (QMS)
- Direct experience authoring, reviewing, and approving Quality/CMC sections for regulatory submissions
- Proven ability to build a high-performing QA organization
Nice to have
- Advanced certifications (e.g., ASQ CQA/CQM)
- Strong preference for experience in Cell/Gene Therapy, Biologics, Tissue Engineering, or Advanced Therapy Medicinal Products (ATMPs)
- Proven track record of successfully hosting regulatory agency inspections and acting as the primary quality liaison
What you get
- Salary range of $191,000 - $202,000 annually
- Equity
- Comprehensive benefits package
- Support for continuous learning and career progression
Worth weighing
- No specific details on the comprehensive benefits package provided
- Role requires extensive experience in a highly regulated environment, which may limit candidates without such a background
- The salary range indicates a competitive compensation but may not reflect the total value of the package without further details
Summarised from Aspect Biosystems's posting. Read the full original.
Listed by Aspect Biosystems on their greenhouse job board, last confirmed open on 2026-11-14. PitchMeAI is not the employer.
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