Quality Control Associate I — Lab Testing & Compliance

Regulatory Toolkit

Frederick (MD)

On-site

USD 56,000 - 119,000

Full time

12 days ago

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Benefits offered by this job

401(k) plan
Health benefits
Paid vacation
Paid holidays

Job summary

AstraZeneca Operations is seeking candidates for an Associate level laboratory role at our Frederick Manufacturing Center. Responsibilities include sampling, testing, data entry, and maintaining a compliant lab environment. You will work under supervision and advance with established SOPs and GMP guidelines.

Essential qualifications involve a science-focused degree or equivalent experience, with 0–5 years in pharma settings. Competitive pay, benefits, and growth opportunities are offered.

Qualifications

  • BS/AS/HS with relevant lab experience in pharma/biotech environments.
  • Experience with routine lab testing and data recording per SOPs.
  • Familiarity with GMP and quality compliance is preferred.

Responsibilities

  • Perform laboratory sampling and testing under supervision.
  • Assist with routine tests and generate laboratory results.
  • Maintain lab housekeeping and stocking.
  • Prepare samples and record results per work plan.
  • Set up and clean testing equipment and sites.
  • Identify equipment or testing issues and report.
  • Ensure equipment and supplies are available for testing.
  • Enter data for compliance and report abnormalities.

Skills

Pipetting
pH measurement
UV/Vis
ELISA
GMP experience
Balances
Written communication
Oral communication
Self-motivation
Multi-tasking

Education

BS in Pharmaceutical Science
Associates degree in science
High school diploma with experience

Tools

Laboratory equipment
SOP compliance
cGMP compliance

Job description

AstraZeneca Operations is seeking candidates for an Associate level laboratory role at our Frederick Manufacturing Center. Responsibilities include sampling, testing, data entry, and maintaining a compliant lab environment. You will work under supervision and advance with established SOPs and GMP guidelines.

Essential qualifications involve a science-focused degree or equivalent experience, with 0–5 years in pharma settings. Competitive pay, benefits, and growth opportunities are offered.

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