Nutraceutical Manufacturing Technician

P4R Wholesale

Orlando (FL)

On-site

USD 40,000 - 60,000

Full time

14 days+

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Job summary

P4R Wholesale, a leader in the nutraceutical industry, is seeking a Manufacturing Technician in Orlando, FL. This full-time role involves operating advanced equipment, ensuring quality control, and collaborating with teams to produce high-quality sterile products. Ideal candidates will have a background in chemistry or biochemistry, strong communication skills, and a commitment to safety and compliance.

Qualifications

Experience in a laboratory or manufacturing environment is beneficial.
Strong understanding of chemical processes and regulatory compliance.
Ability to work collaboratively and maintain safety standards.

Responsibilities

Operate and maintain advanced manufacturing equipment.
Conduct quality control tests and document processes.
Collaborate with R&D and quality assurance teams.

Skills

Clean Rooms

Quality Control

Communication

Troubleshooting

Attention to Detail

Education

Bachelor’s or Doctorate degree in Chemistry

Certifications in manufacturing or quality assurance

Job description

Job Title: Nutraceutical Manufacturing Technician

P4R Wholesale is a recognized innovator in the nutraceutical industry, specializing in the research, development, manufacturing, and production of sterile products. Our commitment to quality, safety, and efficacy ensures that our solutions contribute positively to health and wellness. We are currently seeking a skilled and detail-oriented Manufacturing Technician to assist with our production processes within this specialized laboratory environment.

Role Description

This is a full-time, on-site role located in Orlando, FL. The Manufacturing Technician will be responsible for participating in manufacturing processes, ensuring quality control, maintaining clean rooms, and troubleshooting equipment issues. The ideal candidate will play a critical role in the formulation, production, and quality assurance of high-quality nutraceutical products. Effective communication with team members and adherence to safety and compliance regulations are essential.

Key Responsibilities

Operate and maintain advanced manufacturing equipment to produce sterile products.
Formulate and assist in the development of new sterile products based on scientific principles and market needs.
Conduct quality control tests and analytical procedures to ensure product efficacy and safety, including potency and purity assessments.
Document all manufacturing processes and outcomes meticulously, adhering to Good Manufacturing Practices (GMP) and regulatory standards.
Collaborate with R&D and quality assurance teams to troubleshoot formulations, conduct stability studies, and assess product shelf life.
Maintain accurate inventory of raw materials and finished products; assist in supply chain management as necessary.
Participate in training and continuous education programs to stay updated on industry trends, regulations, and technological advancements.
Ensure compliance with safety regulations, maintaining a clean and organized workspace to prevent contamination.
Support the implementation of quality assurance measures and continuous improvement initiatives within the production environment.

Qualifications

Experience with Clean Rooms and Quality Control procedures
Knowledge of Manufacturing Processes and ability to troubleshoot equipment issues
Strong communication skills and ability to work collaboratively
Strong understanding of chemical processes, laboratory techniques, and regulatory compliance (e.g., FDA, NSF, cGMP, USP 797, Sterile Transfer Technique)
Attention to detail and commitment to maintaining safety and compliance standards
Previous experience in a laboratory or manufacturing environment is beneficial
Bachelor’s or Doctorate degree in Chemistry, Biochemistry, or a related field; additional certifications in manufacturing or quality assurance are a plus.

Seniority Level