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Bilingual Soft Chew Formulator

5th HQ

Job Description

Job Description

Job Title: Soft Chew Formulator

Location: Miramar, FL

Schedule: Monday to Friday, 8:30 AM – 5:00 PM

Job Type: Full-Time

Position Overview:

We are seeking a hands-on and innovative  Bilingual  Soft Chew Formulator to lead our Human Soft Chews production and support the development of new supplement products. This role combines daily production oversight with research & development (R&D) and process improvement responsibilities. The ideal candidate will have a background in chemistry, food science, or a related discipline, and experience in FDA-regulated environments such as nutraceuticals, pharmaceuticals, or food manufacturing.

Key Responsibilities:

  • Oversee daily operations of the Human Soft Chew production area, ensuring adherence to safety, quality, and GMP standards.

  • Supervise and support production staff on the floor, providing guidance and problem-solving as needed.

  • Assist with the formulation and scaling of new soft chew supplement products in collaboration with R&D and leadership.

  • Maintain raw material, packaging, and finished goods inventory.

  • Develop and maintain SOPs, batch records, and GMP-compliant documentation.

  • Monitor inbound and outbound shipments; assist with pickups and logistics when necessary.

  • Handle production-related administrative tasks such as label printing, batch number control, and shipping prep.

  • Identify and support process improvements to enhance efficiency, quality, and consistency.

  • Contribute to broader cross-functional company initiatives, including product innovation and compliance updates.

Qualifications:

  • Bachelor’s degree in Chemistry, Biology, Food Science, or a related field.

  • Bilingual (English and Spanish ) – required to communicate effectively with production staff and cross-functional teams.

  • Minimum of 5 years of experience in a formulation and/or R&D role within an FDA-regulated industry (e.g., nutraceuticals, pharmaceuticals, food, personal care).

  • Strong knowledge of GMP standards and production protocols.

  • Ability to lead, train, and motivate team members in a fast-paced manufacturing environment.

  • Excellent organizational, documentation, and project management skills.

  • Hands-on, collaborative approach with a problem-solving mindset.

Vacancy posted 12 days ago
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