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Merck KGaA, Darmstadt, Germany

Quality Control Technician 2

20h

Merck KGaA, Darmstadt, Germany

US · Full-time · $44,000 – $68,000

About this role

Intermediate-level Quality Control Technician in a membrane analytical lab supporting biopharmaceutical testing operations with a focus on safety, quality, and productivity. Skilled in basic troubleshooting and familiar with Laboratory Information Management Systems. This role does not offer sponsorship for work authorization.

Test membranes safely and in accordance with Standard Operating Procedures, Quality and Safety Specifications and GMP standards. Safely set up and operate quality lab test equipment while monitoring required inputs and outputs. Accurately complete documentation per GMP standards and ensure proper entry into LIMS.

Work in a laboratory environment with exposure to machinery, chemical reagents, and biological materials at Biosafety Levels 1 and 2. Position requires 100% standing or sitting for up to 12-hour shifts along with frequent lifting of 20-30 lbs and regular bending and twisting.

Support quality lab operations and projects under the supervision of senior technicians while developing skills to independently perform membrane analytical testing. Initiate and participate in Out of Specification investigations and assist with execution of protocols, qualifications, and validations.

Requirements

  • 1+ years of laboratory or cGMP manufacturing experience.
  • High school diploma or GED.
  • Basic knowledge of EHS, ISO, cGMP, and other manufacturing regulatory requirements.
  • Basic computer skills and familiarity with Microsoft Office applications.
  • Read, follow and understand test methods, operating procedures and related documentation.
  • Reliable and self-motivated.

Responsibilities

  • Test membranes safely and in accordance with Standard Operating Procedures, Quality and Safety Specifications and GMP standards.
  • Safely set up and operate quality lab test equipment and monitor required inputs and outputs.
  • Support quality lab operations and projects under the supervision of senior technicians.
  • Accurately complete documentation per GMP standards.
  • Initiate and participate in Out of Specification (OOS) investigations.
  • Assist with execution of protocols, qualifications, and validations.
  • Perform basic troubleshooting and equipment set-ups, review and verify test data for accuracy, and ensure proper entry into LIMS.

Benefits

  • Health insurance
  • Paid time off (PTO)
  • Retirement contributions