Chemist I
: Job Details :

Are You a Chemist with 1–3 Years or 3–5+ Years of Experience? We Want You!

Join The Monster Group in Orlando, FL

At The Monster Group, innovation is in our DNA. As an international provider of alternative products, we deliver quality, precision, and unmatched value across our diverse portfolio of brands. From R&D to manufacturing, distribution to marketing—we control every aspect of our process in our state-of-the-art, GMP-certified facility. Now, we're looking for two talented chemists—one early in their career and one seasoned pro—to join our Quality & R&D team.

Whether you're just starting your journey in the lab or you've spent years leading quality control and compliance, there's a place for your expertise here.Chemist I – Quality & R&D (1–3 Years Experience)

This hybrid role blends hands-on formulation and testing with quality documentation and audit readiness. You'll work side-by-side with senior chemists to create and improve product formulas, perform QC testing, and ensure our products meet the highest internal and regulatory standards.

What You'll Do:

• Assist in formulation development and stability testing.
• Conduct quality control testing on raw materials, intermediates, and finished goods.
• Maintain accurate lab records and documentation.
• Support GMP and ISO audits with proper data, calibration logs, and quality reports.
• Keep our lab clean, safe, and compliant.

What You'll Bring:

• Bachelor's in Chemistry (minimum 3.5 GPA preferred).
• 1–3 years in a lab, QC, or GMP-regulated environment.
• Strong lab skills, attention to detail, and familiarity with GMP/ISO standards.

Senior Chemist – Quality & Compliance Lead (3–5+ Years Experience)

If you've mastered quality control systems, regulatory compliance, and audit leadership, this is your opportunity to own the QC process across multiple facilities. You'll lead GMP and ISO compliance efforts, maintain the Quality Management System (QMS), and ensure every product that leaves our facility meets rigorous safety, accuracy, and consistency standards.

What You'll Do:

• Oversee all QC systems, documentation, and compliance requirements.
• Lead GMP and ISO audits from preparation through execution.
• Manage COAs, nutritional panels, and regulatory label reviews.
• Ensure equipment calibration, maintenance, and readiness for inspection.
• Drive continuous improvement within the QMS.

What You'll Bring:

• Bachelor's in Chemistry, Biology, Food Science, or related field (or equivalent experience).
• 5+ years in QC, regulatory compliance, or lab management.
• Proven success in GMP-compliant and ISO-audited environments.
• Strong leadership, technical documentation, and problem-solving skills.

Why The Monster Group?

• Work in a fast-paced, innovation-driven environment.
• Collaborate with a passionate, multidisciplinary team.
• Be part of a company that owns the entire production cycle—giving you influence from concept to consumer.

Location: Onsite in Orlando, FL. Both positions require occasional travel between facilities.

Perks: Competitive pay, benefits, and opportunities for professional growth.