Job Description

Position Summary:

Sunflower Wellness is seeking a detail-oriented, safety-conscious Production Technician to support our cGMP manufacturing operations. This individual will be responsible for executing chemical processes, maintaining equipment and facilities, and ensuring all production activities comply with Good Manufacturing Practices (cGMP CFR 110 and 111). The ideal candidate thrives in a 24/7 manufacturing environment and demonstrates strong documentation skills and commitment to quality standards.

Key Responsibilities:

• Execute chemical reactions, workups, and purification processes using various chemical techniques under supervision of production management.
• Complete batch records accurately, signing off on all production tasks, cleaning activities, and maintenance performed during shift.
• Prepare chemical solutions, monitor processes, and collect samples from production batches for quality testing.
• Operate, maintain, troubleshoot, and clean laboratory equipment according to company SSOPs and cleaning schedules.
• Adjust processing equipment to optimize production efficiency and output.
• Conduct facility sanitation in accordance with cGMP guidelines and company cleaning schedules.
• Handle and dispose of hazardous waste following 6-CCR 1007-3 Part 262 protocols.
• Maintain compliance with all personnel hygiene, handwashing, and PPE requirements to ensure personal and peer safety.
• Participate in required training including HAZWOPER 40, facility contingency plans, emergency protocols, and biannual hazardous waste handling refreshers.

Required Qualifications:

• Experience with lab equipment such as rotary evaporators, flow pumps, vacuum pumps, fluid heaters/chillers, cryo-freezers, incubators, and falling film evaporators.
• High school diploma or equivalent.
• Valid driver's license.
• Minimum 2 years of chemical processing experience in a manufacturing or laboratory setting.
• Strong documentation skills and ability to maintain accurate, detailed records.

Preferred Skills (Nice to Have):

• Experience working in a cGMP environment.
• Good Documentation Practices (GDP) experience.
• Familiarity with batch record systems and quality control procedures.

Why Join Us?

• Gain hands-on experience with advanced chemical processing equipment in a state-of-the-art cGMP facility.
• Develop expertise in pharmaceutical manufacturing standards and regulatory compliance.
• Work alongside synthetic chemists and quality specialists in a collaborative, science-driven environment.
• Be part of a vertically integrated biotechnology company advancing natural product chemistry and pharmaceutical development.

Pay: $24-$30 per hour

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