QC Analytical Specialist, Cell Therapy - 4x10 Shift, Equity

AstraZeneca plc

Rockville (MD)

On-site

USD 81,000 - 121,000

Full time

4 days ago
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Benefits offered by this job

Short-term incentive bonuses
Equity-based awards
Health, dental, and vision coverage
Paid time off

Job summary

AstraZeneca plc in Rockville, MD is seeking a Specialist, Quality Control Analytical for a 4x10 hour shift (Wed-Sat). You will perform routine and non-routine analytical testing to support cGMP lot release and stability of cell therapy products, using flow cytometry, ELISA, PCR, and cell-based assays.

You will operate instruments, maintain documentation, participate in investigations, and contribute to CAPAs.

Qualifications

  • Bachelor's degree in Biological Sciences, Chemistry, Biochemistry, or related discipline.
  • Minimum of 3 years' experience with laboratory techniques relevant to cell therapy or biologics.
  • Hands-on experience with flow cytometry, ELISA, PCR, cell culture, cell count/viability, and related assays.
  • Ability to work on-site in a lab-based role for the assigned shift.
  • Strong cross-functional collaboration and flexible in evolving environment.

Responsibilities

  • Execute QC testing for cell therapy products per approved methods and SOPs.
  • Operate, calibrate, and maintain instruments; document activities.
  • Maintain accurate records; write/review SOPs and test methods; support audits.
  • Participate in laboratory investigations and CAPAs.
  • Provide peer training and maintain analyst proficiency.
  • Coordinate daily testing priorities and communicate testing status.

Skills

Flow cytometry
ELISA
PCR
Cell culture
Cell counting
Viability assays

Education

Bachelor's degree in Biological Sciences

Tools

Flow cytometer
ELISA reader
PCR machine

Job description

AstraZeneca plc in Rockville, MD is seeking a Specialist, Quality Control Analytical for a 4x10 hour shift (Wed-Sat). You will perform routine and non-routine analytical testing to support cGMP lot release and stability of cell therapy products, using flow cytometry, ELISA, PCR, and cell-based assays.

You will operate instruments, maintain documentation, participate in investigations, and contribute to CAPAs.

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