R-262920 Specialist, Quality Control Analytical, Cell Therapy (Sunday - Wednesday)
AstraZeneca · Rockville, Maryland, United States of America · Global
Other
–
Dentist
Demand72
Career growth62
Healthcare fit38
Remote potential–
5-year outlook
Stable demand expected for cell therapy and biologics QC analytical talent, with progression toward senior QC, QA, or lab operations roles; the posted base range is $80,909.60-$121,364.40 plus incentives.
Clinical license
Not required
Applicant reach
narrow
Seniority
mid
Employment type
full-time
Date found
2026-10-28
Intelligence details
Flexible work details
- Engagement type
- Permanent
- Hours
- Full-time
- Eligible countries
- United States
- Profession fit
- Dentist
- Rate period
- Hourly
Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.
Why this is worth applying to
Worth considering only if you have hands-on biologics/cell therapy QC laboratory experience. Most clinicians without bench experience would find the technical barrier and shift pattern poorly aligned with a non-clinical transition.
Who should apply
Biological sciences or biochemistry graduates with 3+ years of cGMP lab experience; cell therapy/biologics QC analysts; lab technologists with flow cytometry, ELISA, PCR, and cell-based assay experience; allied health professionals with strong prior bench research backgrounds.
CV angle
Frame real laboratory and regulated-work experience around cGMP testing, assay execution, data integrity, contemporaneous documentation, instrument troubleshooting, SOP authorship/review, and deviation/OOS/OOT support. Avoid claiming specific cell therapy methods unless genuinely performed.
Skills to highlight
- Flow cytometry
- ELISA
- PCR
- Cell culture and cell-based assays
- cGMP documentation and ALCOA+ data integrity
- OOS/OOT and deviation investigations
- CAPA and change controls
- Instrument calibration and troubleshooting
Role summary
A pharma QC analytical specialist role performing cGMP analytical testing for cell therapy products, including flow cytometry, ELISA, PCR, cell count/viability, and cell-based assays, with responsibility for documentation, instrument maintenance, investigations, and audit readiness.
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