Job Description

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.

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