QC Analyst II

DanaherMadison, WI
94d

About The Position

At Aldevron, we deliver world-class CDMO services that accelerate the development of groundbreaking therapies. Our mission is to be the engine of innovation for genomic medicine pioneers. As a member of our team, you'll help bring life-changing innovations to life—impacting millions around the world. We bring together deep scientific expertise, an unwavering commitment to quality, and a collaborative spirit to drive progress. Whether you're launching your career or bringing years of experience, we value the unique perspective you bring. Join us and become part of a mission-driven team advancing science and unlocking human potential—one discovery at a time.

Requirements

  • Bachelor's degree in Scientific field + 2 years of experience working in an ISO 13485 and/or GxP laboratory environment.
  • Knowledge of analytical laboratory practices and Good Documentation Practices.
  • Have good depth perception, manual dexterity ability, and steady hands for pipetting.

Nice To Haves

  • Prior experience with one or more of: HPLC, 96-well plate assays, CE-SDS, ELISA, qPCR.
  • Experience with Electronic Laboratory Information Management Systems (LIMS).

Responsibilities

  • Independently perform routine QC assays for biological macromolecules (Concentration, Purity, Activity, Residual, Compendial) according to established standard operating procedures under direction from the QC Supervisor.
  • Perform data entry and review own work and peers' work for accuracy in accordance with laboratory and Good Documentation Procedures.
  • Document and compare testing results against control/specification limits, and report all Out of Specification (OOS), Out of Trend (OOT) results and other quality concerns to the QC Supervisor.

Benefits

  • Comprehensive health care program.
  • Paid time off.

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What This Job Offers

Job Type

Full-time

Career Level

Entry Level

Industry

Computer and Electronic Product Manufacturing

Education Level

Bachelor's degree

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