AstraZeneca

Manager Quality Control Analytical (Wednesday - Saturday)

AstraZeneca$112K — $168K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor’s degree in Biological Sciences, Chemistry, Biochemistry, or related discipline; advanced degree (MS/PhD) preferred.
  • At least 5 years' experience in pharmaceutical/biotech QC with emphasis on laboratory operations/management in a cGMP setting.
  • Experience operating a QC laboratory in a regulated environment with knowledge of cell therapy considerations.
  • Proven ability to coordinate laboratory operations and manage competing priorities.
  • Hands-on experience with qualification and maintenance of QC instruments and lab informatics systems.
  • Ability to design and deliver effective training and mentorship.
  • Effective cross-functional partner with various teams in a fast-paced environment.

Responsibilities

  • Manage a QC laboratory team and day-to-day lab activities, including sample intake and testing flow.
  • Perform and oversee QC testing for cell therapy products ensuring adherence to cGMP and data integrity expectations.
  • Maintain accurate records in electronic systems; author/review SOPs and ensure readiness for audits.
  • Train and mentor junior team members on methods, cGMP/GDP, and safety practices.
  • Coordinate testing schedules, sample logistics, and communicate status and risks to stakeholders.
  • Drive continuous improvement and LEAN initiatives to enhance laboratory performance.
  • Implement deviation trend reviews to bolster right-first-time performance.

Benefits

  • Qualified retirement programs.
  • Paid time off including vacation, holiday, and leave.
  • Health, dental, and vision coverage.
Full Job Description

Manager, Quality Control Analytical, Cell Therapy

Wednesday - Saturday (4x 10 hour day shift)

Role Overview 

The Manager, QC Analytical, provides managerial, operational and technical leadership for a cGMP Quality Control laboratory supporting cell therapy lot release and stability testing. The role focuses on right‑first‑time analytical assay execution (e.g., flow cytometry, ELISA, PCR, automated cell counting, and other cell‑based assays) and end‑to‑end laboratory readiness, including people and equipment oversight. Responsibilities span management of a routine testing team, testing execution, laboratory operations management, quality record management, and audit/inspection readiness. The Manager partners closely with other QC teams, MSAT/Analytical Development, Manufacturing, QA, and Supply Chain to ensure the lab operates safely, compliantly, and efficiently to meet patient supply timelines. 

 

This position is for a 4 days per week, 10 hours per day shift, Wednesday through Saturday.  

 

Role Responsibilities 

  • Laboratory operations oversight: Manage a QC laboratory team and day‑to‑day lab activities including sample intake, scheduling, testing flow and data review. 

  • Analytical testing: Perform and oversee QC testing for cell therapy products (flow cytometry, ELISA, PCR, cell based assays, cell count/viability) per approved methods, ensuring adherence to cGMP, GDP, and data integrity expectations (ALCOA+). 

  • Documentation and compliance: Maintain accurate, contemporaneous records in relevant electronic systems and forms; author/review SOPs, test methods, and certificates of analysis; ensure readiness for internal/external audits and regulatory inspections. 

  • Training and mentoring: Train and coach junior team members on methods, cGMP/GDP, safety, and data integrity; support qualification of analysts and ongoing proficiency assessments. 

  • Planning and communication: Coordinate testing schedules, sample logistics, and material controls; communicate status and risks; escalate issues proactively to meet lot release timelines. 

  • Continuous improvement and LEAN: Drive 5S, visual management, standard work, and deviation trend reviews; improve flow and increase right‑first‑time performance. 

 

Minimum Requirements 

  • Bachelor’s degree in Biological Sciences, Chemistry, Biochemistry, or related discipline; advanced degree (MS/PhD) preferred. 

  • At least 5 years' experience in pharmaceutical/biotech QC with emphasis on laboratory operations/management in a cGMP setting.   

  • Demonstrated experience operating a QC laboratory in a regulated environment with knowledge of cell therapy specific considerations (e.g., chain of identity/chain of custody, rapid turnaround for patient supply, phase‑appropriate controls). 

  • Proven ability to plan and coordinate laboratory operations, manage competing priorities, and communicate status, risks, and mitigations tocross‑functionalstakeholders; experience presenting in audits/inspections.

  • Hands‑onexperience with qualification and maintenance of key QC instruments and with lab informatics (LIMS/ELN/LES, instrument data systems); strong command of data integrity controls and computerized systems compliance.

  • Ability to design and deliver effective training; mentor analysts on safe, compliant, and efficient lab practices; cultivate a culture of quality and continuous improvement.

  • Effectivecross‑functionalpartner with Manufacturing, MSAT/AD, QA, Supply Chain, Facilities, and EHS; comfortable operating in a fast‑changingenvironment and adjusting plans to meet patient‑criticaltimelines.

  • Ability to work on-site in a lab-based rolefor the assigned shift.

The annual base pay (or hourly rate of compensation) for this position ranges from $112,604.80 -  $168,907.20. Our positions offer eligibility for various incentives—an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.

Date Posted

05-Jun-2026

Closing Date

18-Jun-2026

About AstraZeneca

AstraZeneca is a British-Swedish multinational pharmaceutical company that specializes in the research, development, and manufacturing of prescription drugs. The company was formed in 1999 through the merger of Astra AB and Zeneca Group plc. AstraZeneca's products are used to treat a wide range of medical conditions, including cancer, cardiovascular disease, respiratory disease, and diabetes. The company has operations in over 100 countries and employs more than 76,000 people worldwide. AstraZeneca is committed to developing innovative medicines that improve the health and well-being of people around the world.
Learn more about AstraZeneca
Size
83,100 employees
Market Cap
$211.5 billion
Industry
Net Income
$3.1 billion
Founded
1999
5 Year Trend
+10.2%
Revenue
$26.6 billion
NASDAQ

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