Laboratory Chemist - Quality Control

Step into a critical role supporting the production of human and veterinary pharmaceutical products within a GMP-regulated manufacturing environment. This position offers the opportunity to work hands-on with advanced analytical instrumentation, contribute to product quality and compliance, and support ongoing growth tied to new product launches and validation activities. This is an ideal opportunity for a chemist who thrives in a structured, fast-paced laboratory setting and is looking to build long-term stability within a manufacturing-driven organization.What You’ll Be Doing Perform chemical analysis on raw materials, in-process samples, finished products, and stability samples Operate, calibrate, and maintain analytical instrumentation including HPLC, GC, and related systems Prepare reagents and samples in accordance with SOPs and cGMP requirements Accurately document and report analytical results following established quality standards Support method development, validation, and transfer activities Investigate and troubleshoot analytical or equipment-related issues Collaborate cross-functionally with production, QA, and other departments Mentor and support junior laboratory staff as neededRequired Experience & Qualifications 3–5 years ofdirect, hands-on chemistry experience in a GMP-regulated environment(non-academic) Strong experience withchromatography techniques(HPLC, GC, UV/VIS, FTIR, etc.) Proven background inQuality Control or manufacturing laboratory settings Experience with analytical instrumentation such asAA, IC, ICP-MS, and dissolution testing Familiarity withcGMP standards and quality systems(deviations, CAPAs, change control) Proficiency with laboratory software systems (e.g., Empower, Microsoft Office) Strong attention to detail, documentation accuracy, and time managementNote:Academic-only or research-based lab experience will not be considered. Industry experience is required.Physical Requirements Ability to lift 50 lbs. regularly Ability to stand, walk, or sit for extended periods (8+ hours/day)Work Environment & Opportunity On-site role within an FDA-regulated pharmaceutical manufacturing facility Exposure to both liquid and solid dose production environments Opportunity to supportnew product introductions and validation efforts Stable manufacturing setting with consistent production demandAdditional Highlights Competitive hourly compensation with flexibility based on experience PTO accrual with potential for negotiation Approximately 22 annual company-observed closure days aligned with holiday schedules Relocation assistance available on a case-by-case basis Located near the Gulf Coast with access to a low cost of living and proximity to major regional hubs