Quality Control Analyst II

Quality Control Analyst II Astrix Technology Group - 3.4 Fort Worth, TX Job Details Contract 6 hours ago Benefits Health insurance Dental insurance Paid time off 401(k) matching Qualifications Instrumentation troubleshooting Laboratory equipment performance testing and validation Procedural guides Pharmaceutical laboratory environment Preventive action implementation Laboratory instrument validation Production deviation management Corrective and preventive actions (CAPA) GMP Equipment malfunction troubleshooting Mid-level Laboratory equipment calibration Pharmaceutical company experience Laboratory standard operating procedures Compliance documentation Quality compliance management Vendor relationship management Laboratory preventive maintenance Vendor communication Verification of laboratory test methods Quality control within pharmaceutical industry Equipment testing Investigating compliance violations Test validation method Standard operating procedures (SOPs) Communication skills Audit support Documentation reviews Full Job Description Exciting Quality Control Analyst II (Contract -) development opportunity to work for a global leader dedicated to helping people see brilliantly. The largest device company in the world - with complementary businesses in Surgical and Vision Care.

Location:

Fort Worth, TX (Onsite)

Contract:

1 year Contract extension or conversion potential

Benefits:

Medical, Dental, Holiday, PTO 401K matching We are seeking a Quality Control Analyst II to support laboratory instrumentation compliance and qualification activities in a GMP-regulated environment. The primary focus of this role is laboratory instrument Preventive Maintenance (PM), Calibration (PC), Performance Verification (PV), and new equipment qualification. CSA/CSV experience is highly preferred.

Key Responsibilities:

Coordinate PM, calibration, PV, and qualification activities for laboratory instruments. Troubleshoot equipment issues and support vendor management. Execute equipment qualifications, method validations, and transfers. Support deviations, investigations, CAPAs, and audit readiness. Maintain SOPs, protocols, and compliance documentation. Review laboratory data and ensure adherence to GMP requirements.

Qualifications:

Experience in a regulated pharmaceutical, biotech, or medical device laboratory. Knowledge of laboratory instrumentation, qualification, and compliance processes. CSA/CSV experience preferred. Strong documentation, troubleshooting, and communication skills. This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you! INDBH #LI-RL1