Job Details

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 needed

Required Experience & Qualifications

• 3–5 years of direct, hands-on chemistry experience in a GMP-regulated environment (non-academic)
• Strong experience with chromatography techniques (HPLC, GC, UV/VIS, FTIR, etc.)
• Proven background in Quality Control or manufacturing laboratory settings
• Experience with analytical instrumentation such as AA, IC, ICP-MS, and dissolution testing
• Familiarity with cGMP 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 management

Note: 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 support new product introductions and validation efforts
• Stable manufacturing setting with consistent production demand

Additional 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