Quality Control Technician 3

The businesses of Merck KGaA, Darmstadt, Germany•Jaffrey, NH

1d•$19 - $30•Onsite

About The Position

Advanced Lab Quality Control Technician with expertise in bacterial testing of biopharmaceutical filtration membranes and devices, focused on ensuring safety, quality, and productivity. Experienced in supporting advanced testing operations through troubleshooting, process setup, and retention testing procedures. Proficient in using Laboratory Information Management Systems (LIMS) to accurately track and document results. Shift hours : 10PM -6AM

Requirements

3+ years of laboratory experience.
High school diploma or GED.
Must be able to grasp, manipulate and handle objects consistently and regularly, Fine motor skills are required.
Pass a visual acuity test.

Nice To Haves

Associate’s degree in Life Science discipline.
Bachelor’s degree in any discipline.
3+ years’ experience in an aseptic and cGMP laboratory environment.
1+ years of experience with Laboratory Information Management Systems.
Strong knowledge of EHS, ISO, cGMP, and other laboratory and regulatory requirements.
Demonstrated computer skills, familiarity with Microsoft Office applications.
Reliable and self-motivated.
Read, follow and understand Test Methods, Test Specifications, and other technical documentation.

Responsibilities

Test products safely and in accordance with Standard Operating Procedures, Quality and Safety Specifications and GMP standards.
Follow procedures to perform required testing independently.
Safely set up and operate quality lab test equipment and monitor required inputs and outputs on equipment such as steam systems, pressurized vessels, bacterial challenge systems, and various test stands and support equipment.
Support quality lab operations and projects under the supervision of master technicians.
Proactive identification of safety, quality, and productivity concerns. Actively report hazardous conditions or hazardous behaviors observed in the work center and the site.
Participate in laboratory audits and tours, perform troubleshooting and advanced set-ups, review and verify test and process data with accurate entry into the Laboratory Information Management System (LIMS), support sustainability initiatives, and operate effectively with limited supervision.
Accurately complete and review documentation in compliance with GMP standards, initiate and participate in Out of Specification (OOS) investigations, support the execution of protocols, qualifications, and validations, and maintain a clean, organized, and compliant workspace.