Analytical Scientist I

📍 Miami, FL | On-Site

💲 Salary: $55,000 - $62,500 + Benefits

Our client, a well-established pharmaceutical and consumer healthcare manufacturer, is seeking an Analytical Scientist I to join their Research & Development team in Miami, Florida. This is an excellent opportunity for an early-career scientist looking to grow within a regulated pharmaceutical environment and gain hands-on experience supporting product development and analytical method activities.

Position Overview

The Analytical Scientist I will support analytical development efforts through testing of raw materials, in-process samples, and finished products. This role will participate in method transfer, verification, and validation activities while ensuring compliance with cGMP regulations and data integrity standards.

Key Responsibilities

• Perform analytical testing on raw materials, in-process materials, and finished products.
• Execute method transfer, verification, and validation protocols.
• Evaluate, analyze, and interpret analytical data and test results.
• Document laboratory activities, data, and results in accordance with SOPs, cGMP requirements, and data integrity guidelines.
• Prepare analytical methods, technical reports, and supporting documentation.
• Maintain laboratory equipment through routine calibration and upkeep.
• Manage laboratory inventory, including chemicals, supplies, and glassware.
• Support general laboratory organization and maintenance activities.
• Collaborate with R&D and cross-functional teams to support product development initiatives.
• Perform additional duties as assigned.

Qualifications

• Bachelor's or Master's degree in Chemistry or a related scientific discipline.
• 1–3 years of analytical laboratory experience within the pharmaceutical, biotechnology, consumer healthcare, or related industry.
• Experience utilizing analytical techniques to support product development activities.
• Strong understanding of analytical chemistry principles and laboratory instrumentation.
• Knowledge of current Good Manufacturing Practices (cGMP).
• Excellent organizational skills with the ability to manage multiple priorities in a fast-paced environment.
• Strong written and verbal communication skills.
• Proficiency with basic computer applications and scientific documentation practices.

Schedule

• Monday – Friday
• 8:00 AM – 4:30 PM

Application Period: This position opens for applications on 6/3/2026 and will remain open for a minimum of 30 days from the posting date.

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