Regulatory Affairs Specialist I

Unicity International, Inc.; Provo (UT); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Health benefits

Dental benefits

Vision benefits

Life insurance

Parental leave

Vacation days

Job summary

Unicity USA Inc in Provo is seeking a Regulatory Affairs Specialist to manage registrations across markets and ensure label compliance. You’ll own dossiers from gathering to approval and coordinate with colleagues, manufacturers, and regulators globally.

This in-office role requires attention to detail, strong communication, and the ability to manage multiple submissions under deadlines. You’ll report to the Regulatory Manager and help enable global product launches.

Qualifications

• Bachelor’s degree in science or related field, or equivalent regulatory affairs experience.
• Clear, professional written and verbal communication, including with non-native English speakers.
• Strong organizational skills to manage submissions across markets.
• Close attention to detail on labels, documents, and data.
• Follow-through under deadline pressure.

Responsibilities

• Own product registrations for a designated set of markets, preparing and submitting dossiers.
• Review labels, ingredient lists, and claims against market requirements.
• Gather technical documents from manufacturers (certificates of analysis, specifications, and certificates of free sale).
• Write internal regulatory documents, including market requirement summaries and registration status reports.
• Coordinate with international offices, outside consultants, and government agencies.
• Advise product development teams on formulation and claims for launches in target markets.
• Keep registrations on schedule to meet product launch deadlines.
• This is an in-office position.
• This position will report to the Regulatory Manager.

Skills

Communication skills

Organizational skills

Attention to detail

Deadline driven

Education

Bachelor's degree in science or technical field

Job description

Career Opportunities with Unicity USA Inc

A great place to work.

Careers At Unicity USA Inc

Current job opportunities are posted here as they become available.

Unicity is dedicated to developing innovative, science-based products and programs that promote metabolic health and improve the quality of life for people everywhere. For over 30 years, Unicity has been dedicated to developing high-quality products that contain the vital nutrients your body needs. With the proper process, cutting-edge technology, and a mission to Make Life Better, Unicity is paving the way for a better tomorrow

The Role

Help bring nutritional and personal care products to customers in more than 30 markets across six continents. You'll own product registrations from document gathering to approval, review labels for compliance, and work with colleagues, manufacturers, and regulators around the world. This role suits a detail-oriented person who wants to build a career in global regulatory affairs. The Regulatory Affairs Specialist will sit in our Provo office.

What you'll do

• Own product registrations for a designated set of markets across our 30+ country operations, preparing and submitting dossiers and tracking each through approval.
• Review product labels, ingredient lists, and claims against each market's requirements.
• Gather technical documents from manufacturers, such as certificates of analysis, specifications, and certificates of free sale.
• Write internal regulatory documents, including market requirement summaries and registration status reports.
• Coordinate with our international offices, outside consultants, and government agencies.
• Advise product development teams on formulation and claims so new products can launch in target markets.
• Keep registrations on schedule to meet product launch deadlines.
• This is an in-office position.
• This position will report to the Regulatory Manager.

What you'll bring

• A bachelor's degree in a science or technical field (such as chemistry, biology, nutrition, or food science), or equivalent regulatory affairs experience.
• Clear, professional written and verbal communication, including with non-native English speakers.
• Strong organization: you can manage many submissions across markets without losing track.
• Close attention to detail on labels, documents, and data.
• Follow-through under deadline pressure.

Nice to have

• 1–3 years in regulatory affairs for dietary supplements, foods, or cosmetics.
• Familiarity with international regulations or agencies (for example FDA, Health Canada, EU, ASEAN, China NMPA).
• Understanding of the direct sales business model.
• A second language.

You’ll see a product go from formula to shelf in dozens of countries, and you’ll learn how regulation works around the world. We’re a growing, global team that gives new specialists real ownership early.

In addition to competitive pay, we offer:

• Health, dental, vision, life and other benefits that begin within a month
• Paid parental leave
• Generous vacation allowance in addition to company-paid holidays