Quality Control

  • location: Minneapolis, MN
  • type: Contract
  • salary: $33 - $51 per hour


Chat with me now! - https://flashrecruit.com/jobs/296752

Job Title: Quality Control Analyst II

Position Description

  • Perform supportive activities for general lab readiness, laboratory equipment qualification and method transfers.
  • Conduct critical biological test methods including samples generated for in-process, drug substance and stability.
  • Use a variety of laboratory instrumentation and computer systems to collect and record data (such as LIMS).
  • Follow SOPs to perform methods requiring precise analytical skills and understanding of biology and chemistry principles.

Position Responsibilities

  • Demonstrate a functional understanding of a laboratory setting and Standard Operating Procedures (SOPs).
  • Complete all testing, including special project / protocol testing in a timely and appropriate manner.
  • Maintain data integrity and ensure compliance with company SOPs, specifications and cGMP regulations.
  • Exercise judgment within defined Quality Control procedures and practices to determine appropriate action.
  • Initiate low severity level deviations, CAPAs and change controls within the electronic Quality Management System.
  • Occasionally participate in functional efforts involving teams to solve problems of moderate scope where analysis of situations or data requires a review of identifiable factors.
  • Author minor revisions to existing SOPs.
  • Receives general instructions on routine work and detailed instructions on new assignments.
  • May be required to work overtime or be assigned to a different shift as needed.
  • May perform equipment maintenance and calibrations as required.
  • May perform other duties as assigned.

Position Requirements

  • Bachelors or Masters Degree in any Life Sciences with relevant laboratory coursework and 0-3 years of relevant experience.
  • Previous experience in a regulated environment desirable.
  • Ability to handle multiple tasks concurrently, and in a timely fashion.
  • Must have basic understanding of laboratory instrumentation.
  • Must be able to communicate effectively with supervisors and peers.
  • Must be able to read, write and converse in English.
  • Must be computer literate. Able to navigate, conduct searches, and complete online forms on Personal Computer for the purposes of training, performance management, and self service applications.
  • Good interpersonal skills and be able to work effectively and efficiently in a team environment.
  • Knowledge of cGMP manufacturing preferred.
  • Knowledge of basic chemical and biological safety procedures.
  • Must display eagerness to learn and continuously improve.
  • Must have the following personal attributes: integrity and trust, work ethic, sound judgment, intellectual honesty, pragmatism, courage and conviction.


  • Medical, Dental, and Vision Insurance
  • 401K Plan with Company Match
  • Life and AD&D Insurance

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