Technical Document Supervisor

Company Profile

At Melaleuca:
The Wellness Company, we believe in empowering people to live healthier, more vibrant lives. For over 40 years, we have stood by our mission through integrity, innovation, and care.

We’re proud to operate as a privately held, debt-free company, and in our four decades of growth we’ve never had a layoff—a testament to our commitment to our team and our values.

Our culture is built on trust, excellence, and teamwork—and it shows. Melaleuca has recently been recognized by USA Today as one of America’s Best Stores (for outstanding product quality, customer service, shopping experience, and more). We were also named one of USA Today’s Most Trusted Brands for 2025. For multiple years, Forbes has honored Melaleuca as one of America’s Best Employers, celebrating our workplace culture, stability, and growth opportunities.

If you’re a technically minded leader passionate about regulatory compliance, collaboration, and building high-integrity systems, this role may be your next purpose-driven opportunity.

Overview

Reporting to the R&D International Project & Documentation Manager (or a higher R&D leadership role), the R&D Technical Document Supervisor leads the creation, review, and maintenance of all technical documentation necessary for global product registrations (excluding China). You’ll act as a central bridge between R&D, Regulatory, QA, Operations, and international teams to ensure each product dossier meets safety, efficacy, stability, and compliance requirements across diverse markets.

You will also oversee (or mentor) the Technical Document Specialist role, ensuring consistency and quality across all registration deliverables.

Responsibilities

• Serve as a key member of global, cross-departmental teams (R&D, Regulatory, Marketing, Operations, QA, Purchasing) to understand and navigate each country’s regulatory and business landscape.
• Prepare and maintain essential documentation: formulations, nutrition facts, raw material support, packaging specs/compatibility, processing/flow charts, etc., for product registration in global markets (e.g. Korea, Japan, Taiwan, Hong Kong, Australia, Singapore, UK, US, etc.), excluding China.
• Liaise with Researchers, Formulators, Scientists, and Product Managers to compile technical data and supporting evidence for new and existing product registrations across categories (Personal Care, Ecosense, Pharmacy, Pure, VFL).
• Develop technical dossiers detailing safety, efficacy, test results, bridging data, and justification narratives to satisfy registration requirements.
• Maintain and archive both current and historical records for all global registration documents.
• Collaborate with formulators to define test specifications, compatibility, preservation requirements, and challenge test protocols.
• Manage stability, shelf life, preservation, compatibility, bridging, re-registration, and change notifications for global products.
• Execute change control logic and support bridging documentation when product/packaging/ingredient updates are made.
• Lead process improvement efforts: identify gaps in data systems, propose new tools, web/portal enhancements, or databases to streamline documentation workflows.
• Prepare data summaries, charts, conclusions, and executive-level narratives to support decision making.
• Represent the R&D documentation function in cross-functional meetings, ensuring alignment with Regulatory, Marketing, QA, Purchasing, and International groups.
• Solicit and collate technical information from suppliers (bulk, turnkey, ingredients) to support registration files.
• Liaise closely with Regulatory teams to maintain current formats, standards, and submission processes in each market.

• Provide guidance or oversight to one or more Technical Document Specialists, ensuring consistency, accuracy, and adherence to process standards.
• Mentor or develop junior documentation staff as needed, facilitating training, review, and feedback cycles.

Qualifications

Education & Experience

• Bachelor’…