QC Data Analyst at Medvacon Life Sciences
Medvacon Life Sciences · Houston, United States Of America · Onsite
- Professional
- Office in Houston
This is a 1099 Contract-to-Hire position with no benefits. Estimated 3-month contract.
Position Summary
The QC Data Analyst is responsible for collecting, organizing, analyzing, and interpreting data from multiple laboratory and manufacturing sources to support Quality Control (QC) operations within a pharmaceutical environment. This role will focus on trending, visualization, and data integrity to ensure proactive identification of quality trends and support continuous improvement efforts.
Key Responsibilities
Education:
Position Summary
The QC Data Analyst is responsible for collecting, organizing, analyzing, and interpreting data from multiple laboratory and manufacturing sources to support Quality Control (QC) operations within a pharmaceutical environment. This role will focus on trending, visualization, and data integrity to ensure proactive identification of quality trends and support continuous improvement efforts.
Key Responsibilities
- Collect, compile, and validate QC data from various systems and electronic laboratory notebooks.
- Perform data analysis to identify trends, shifts, and anomalies in analytical results, environmental monitoring, stability studies, and manufacturing data.
- Develop and maintain Excel-based dashboards, graphs, pivot tables, and trend charts for QC data reporting and visualization.
- Support routine QC data trending reports, annual product reviews, and quality metrics summaries.
- Collaborate with QC, QA, Manufacturing, and other departments to interpret and communicate data findings.
- Ensure data accuracy, completeness, and compliance with cGMP and data integrity principles (ALCOA+).
- Assist in investigations, CAPAs, and OOS/OOT analysis through data-driven insights.
- Maintain documentation and records in compliance with regulatory and company standards.
- Support continuous improvement of QC data management processes and reporting tools.
Education:
- Bachelor’s degree in a scientific or technical field (e.g., Chemistry, Biochemistry, Biology, Data Science, Statistics, or related discipline).
- 2–5 years of experience in Quality Control, Data Analysis, or related role in the pharmaceutical or biotechnology industry.
- Experience with GMP-regulated environments preferred.
- Strong proficiency in Microsoft Excel (advanced formulas, pivot tables, macros, and data visualization).
- Experience with data analysis and statistical trending.
- Familiarity with QC laboratory systems (e.g., LIMS, Empower, SAP) is an asset.
- Excellent attention to detail and data accuracy.
- Strong communication skills to present data and trends clearly to technical and non-technical audiences.
- Ability to manage multiple data sources and deliver reports within defined timelines.
- Experience with data visualization tools (e.g., Power BI, Tableau) a plus.
- Understanding of cGMP, GLP, and data integrity requirements.
- Statistical knowledge (control charting, capability analysis, regression).
