# Quality Control Analyst II

**Company:** [BioPharma Consulting JAD Group](null/companies/pScfjBzGATtPx3geL93jwD.md)
**Location:** Fort Worth, United States
**Workplace:** on site
**Employment type:** Contract

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## Description

We are seeking a **Quality Control Analyst II** to support laboratory testing, method development and quality operations at a manufacturing site in Fort Worth, Texas.

**Key Responsibilities**

-   Conduct routine and non-routine analyses of in-process materials, raw materials, environmental samples, finished goods and stability samples.
-   Develop and qualify new testing methods; perform validations or transfers of analytical methods per applicable policies and guidelines.
-   Prepare or review method transfer documentation, including technical transfer protocols and reports.
-   Interpret test results against specifications and control limits and recommend whether data is appropriate for release.
-   Participate in out-of-specification (OOS) and failure investigations and recommend corrective actions; investigate or report questionable results.
-   Write technical reports and documentation such as deviation reports, testing protocols and trend analyses; write or revise QC standard operating procedures.
-   Calibrate, validate and maintain laboratory equipment; identify and troubleshoot equipment problems.
-   Receive and inspect raw materials and perform visual inspections of finished products.
-   Coordinate testing with contract laboratories and vendors, and review their data for accuracy and regulatory compliance.
-   Supply QC data for regulatory submissions and participate in internal assessments and audits.
-   Serve as technical liaison between Quality Control and other departments, vendors or contractors.
-   Train other analysts on laboratory procedures and assays; ensure lab cleanliness and safety standards are maintained.
-   Evaluate new technologies and methods and recommend improvements to analytical procedures.

## Requirements

**Education**

-   Bachelor's degree in Chemistry, Biochemistry, Biology or a related scientific field

**Preferred Experience**

-   Capillary electrophoresis
-   HPLC/GC
-   Analytical instrument qualification

**Key Skills**

-   Analytical method development, qualification, validation and transfer
-   OOS/deviation investigations and root cause analysis
-   Technical writing: protocols, reports, SOPs and trend analyses
-   Laboratory equipment calibration, maintenance and troubleshooting
-   Knowledge of GMP/GDP and regulatory compliance in a quality control laboratory
-   Ability to train others and work cross-functionally with vendors and contract laboratories

## Benefits

-   **Contract position:** 12 months, with possible extension
-   **Shift:** Administrative shift
-   **Days:** Monday to Friday, 40 hours/week
-   On-site in Fort Worth, Texas