Associate QC Analyst – Data-Driven Quality in Biotech

Regeneron Pharmaceuticals, Inc (USA)

City of Rensselaer (NY)

On-site

USD 30,000 - 47,000

Full time

3 days ago
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Benefits offered by this job

Annual bonus
Equity awards
401(k) company match
Health and wellness programs
Fitness centers
Insurance benefits (medical, dental, ?
Paid time off
Family support benefits

Job summary

Regeneron Pharmaceuticals, Inc is seeking a candidate to perform a variety of chemical or biological analyses on raw materials, in-process materials, products, and stability samples to support the quality program.

The role involves gathering data, reviewing results for compliance, calibrating instruments, maintaining SOPs, and contributing to method development and validation efforts across quality systems.

Qualifications

  • Requires BS/BA in Life Sciences or related field; will substitute relevant experience for education.

Responsibilities

  • Gathers data and documents test results.
  • Reviews test results to ensure compliance with standards; reports any quality anomalies.
  • Complies with all pertinent regulatory agency requirements.
  • Participates in required training activities.
  • Maintains laboratory supplies.
  • Conducts testing on raw materials, in-process, product, stability, and/or research samples.
  • Writes and revises control test procedures and SOPs.
  • Completes test records and reviews data.
  • Calibrates or verifies calibration of instruments/devices prior to use.
  • Interacts with outside customers or functional peer groups.
  • May be responsible for maintaining a specific project.
  • May devise or develop new analytical methods and techniques.
  • May assist in validation of methods.
  • May be involved in establishing the transfer of methodology from R&D.

Job description

Regeneron Pharmaceuticals, Inc is seeking a candidate to perform a variety of chemical or biological analyses on raw materials, in-process materials, products, and stability samples to support the quality program.

The role involves gathering data, reviewing results for compliance, calibrating instruments, maintaining SOPs, and contributing to method development and validation efforts across quality systems.

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