**We’re Hiring: Quality Assurance Investigator / Quality Control Specialist**
We’re looking for a hands-on **QA/QC professional** who enjoys working close to the science and cares deeply about product quality, compliance, and continuous improvement.
If you have experience in a **cGMP-regulated pharma or biotech environment** and want to grow your career in quality operations, this could be a great fit.
What You’ll Do
* Execute and maintain Quality Control procedures in line with **cGMP, FDA regulations, and internal quality standards**
* Perform routine **sampling, testing, and data review** for raw materials, in-process samples, finished products, and environmental monitoring
* Investigate deviations, assay failures, and OOS results; support **CAPA and root-cause analysis**
* Support **method validation, method transfers, and equipment qualification**
* Collaborate closely with manufacturing, quality, and technical teams to improve lab and process efficiency
* Maintain accurate, audit-ready documentation and support **regulatory inspections and audits**
What We’re Looking For
* Bachelor’s degree in **Biology, Chemistry, Biotechnology, Life Sciences**, or a related field
* **1+ year of experience** in QA/QC or Quality Systems within a cGMP environment
* Practical experience with **deviations, investigations, and CAPA** (TrackWise experience is a plus)
* Solid understanding of **cGMP, FDA regulations**, and quality systems (cell therapy / CAR-T exposure is a bonus)
* Strong communication skills and the ability to work effectively across teams
* Flexibility to support shift work, occasional overtime, and limited travel when needed
Compensation
Salary Range: $100,000 – $110,000 (based on experience)
Please send your resume to **[Hr@trovetechs.com](mailto:Hr@trovetechs.com)** or reach out directly via LinkedIn.
If you’re interested—or know someone who would be a strong fit—feel free to comment, message, or share this post.
Let’s build quality the right way.
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