Cell & Gene Therapy (CGT) Manufacturing Specialist
Sample Resume & ATS Keywords
Barrington James's 2026 Outlook projects the cell & gene therapy market will reach $54.4bn by 2030, cites 45 FDA-approved CGT products and 700+ active US clinical assets as of 2025, and names MSAT/process development, quality, and cold-chain/logistics among the highest-demand 2026 CGT hiring functions, stating plainly that 'manufacturing readiness is now a primary determinant of funding, valuation, and hiring.' This title is distinct from a generic Process/Manufacturing Engineer role — it's a narrower, hands-on operational specialization in viral-vector production, cell processing, and chain-of-identity logistics. The example below shows how a CGT manufacturing specialist resume carries modality-specific vocabulary distinct from generic process-engineering language.
All sample resume content on this page is original and illustrative — fictional candidates, realistic numbers. Use it as a pattern, not a template to copy verbatim.
Sample Cell & Gene Therapy (CGT) Manufacturing Specialist resume summary
What a parseable, keyword-complete professional summary looks like for this role:
Cell & Gene Therapy Manufacturing Specialist (BS, Cell Biology) with 5 years in GMP-compliant viral-vector production and autologous cell-processing operations. Executes apheresis intake, cell processing, and cryopreservation workflows within cleanroom suites, maintains chain-of-identity/chain-of-custody documentation across patient-specific batches, and supports potency-assay sample handling. Experienced with AAV and lentiviral vector production platforms in a commercial-scale ATMP facility.
Sample achievement bullets that pass ATS screening
Each bullet follows the pattern recruiters and parsers reward: exact keywords, a specific action, and a quantified outcome.
- Executed GMP-compliant viral-vector production runs (AAV and lentiviral platforms) across 60+ batches annually, maintaining a 94% batch success rate.
- Managed chain-of-identity/chain-of-custody documentation for 150+ patient-specific autologous cell-therapy batches, achieving zero identity-mismatch events.
- Performed apheresis-intake and cell-processing operations in a cleanroom GMP suite, processing 8-10 patient samples per week within validated cycle-time targets.
- Executed cryopreservation and cold-chain handoff procedures for 200+ cell-therapy product units, maintaining 100% compliance with temperature-excursion-free storage.
- Supported potency-assay sample preparation and chain-of-custody handoff for 40+ release-testing samples per quarter, contributing to on-time batch disposition decisions.
- Participated in scale-up of a viral-vector production process from lab-scale to a 50L bioreactor, increasing vector yield by 35% while maintaining GMP compliance.
- Executed batch-record documentation for cleanroom operations under 21 CFR Part 11, achieving a 99% right-first-time documentation rate across 2 audit cycles.
- Trained 5 new manufacturing associates on aseptic technique and chain-of-identity procedures specific to autologous cell-therapy production.
ATS keyword bank for Cell & Gene Therapy (CGT) Manufacturing Specialist resumes
From our 2026 research into recruiter sourcing behavior for this role. Recruiter and ATS searches match exact strings — carry the terms your real experience supports, in the wording the posting uses.
| Keyword group | Terms recruiters search |
|---|---|
| Titles & variants | Cell & Gene Therapy Manufacturing Specialist · CGT Manufacturing Associate · ATMP Manufacturing Specialist · Viral Vector Manufacturing Technician · Cell Therapy Process Specialist |
| Credentials | BS/MS in Biotechnology or Cell Biology · GMP manufacturing training · aseptic technique certification |
| Systems & software | MES batch record systems · cleanroom monitoring software · chain-of-identity tracking systems |
| Regulatory/technical vocabulary | viral-vector production · cell processing · apheresis · cryopreservation · chain-of-identity/chain-of-custody · ATMP regulatory framework |
| Quantified outcomes | batches processed · vector yield improvement · cleanroom/GMP suite scale · batch success rate |
Cell & Gene Therapy (CGT) Manufacturing Specialist resume formatting: do this, not that
Do
- Name the specific modality you've worked in: viral-vector production, autologous or allogeneic cell processing, apheresis — not just "biomanufacturing".
- State "chain-of-identity/chain-of-custody" explicitly — this is the operational layer that separates CGT roles from broader process-engineering language.
- Reference ATMP-specific regulatory vocabulary where relevant, distinct from small-molecule/biologics GMP language a generic process-engineer resume defaults to.
- Quantify batches processed, vector types handled, and cleanroom/GMP suite scale — these numbers show real production-scale experience.
- Name the vector platform specifically (AAV, lentiviral, retroviral) if you've worked with it — recruiters in this niche search by platform.
Don't
- Don't write "worked in biomanufacturing" — name the modality (cell processing, viral-vector production) recruiters specifically search for in CGT postings.
- Don't omit chain-of-identity/chain-of-custody experience if you have it — it's the defining operational distinction of patient-specific cell therapy work.
- Don't use generic process-engineering language if your experience is CGT-specific — it dilutes the match against CGT-focused postings.
- Don't leave out batch-success or yield metrics — these are the concrete numbers hiring managers use to compare production-floor experience.
- Don't skip potency-assay or release-testing support experience if you've done it — it signals broader involvement in the CGT product lifecycle beyond core processing.
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