Company Details

Company: US Pharmatech NV, Inc.

Location: Las Vegas, Nevada

Company Details

Company: US Pharmatech NV, Inc.

Location: Las Vegas, Nevada

Job Details

Job Type: Full-time (On-site)

Pay: $45,000 - $60,000 a year based on experience

Benefits: Health Insurance, Dental Insurance, Paid Holiday, Paid Sick Hour, Vacation

Shift & Schedule: Day time (9:00 a.m. – 5:30p.m.) with occasional evening availability required to accommodate communication with Korea-based clients.

Company Overview:

USP NV, Inc. is a Nevada-based contract manufacturer and quality assurance center specializing in the formulation, testing, and export of dietary supplements and functional health products. Our company supports global clients, particularly Korean health brands, by providing end-to-end manufacturing, quality documentation, and regulatory support to meet both U.S. FDA and Korean MFDS (Ministry of Food and Drug Safety) standards.

We manage the entire export quality assurance process, including raw material testing, in-process inspection, finished product release, and bilingual technical documentation for cross-border compliance.
 

Our facility operates under cGMP certification, ISO-based quality systems, and strict traceability requirements to ensure consistent product safety and quality for international markets.

Position Summary:

We are seeking a Quality Assurance Technician who possesses strong bilingual (English/Korean) communication skills and a solid background in quality control, product testing, and regulatory compliance. The successful candidate will work closely with both our U.S. based QA team and Korean partner manufacturers to ensure that all exported products meet the rigorous quality and documentation standards required for MFDS (Ministry of Food and Drug Safety) registration and import approval.

Key Responsibilities:

Duties and responsibilities include, but not limited to, the following and must be performed with limited supervision.

• Conduct raw material, in-process, and finished product testing using established analytical and microbiological methods.
• Review, verify, and maintain batch production records, test results, and Certificates of Analysis (COA) for accuracy and compliance.
• Support and enforce cGMP, FDA, and MFDS quality standards across production and packaging operations.
• Participate in internal audits, deviation investigations, CAPA (Corrective and Preventive Action), and root cause analysis to prevent recurrence of quality issues.
• Ensure calibration and maintenance of laboratory instruments and environmental monitoring systems.
• Coordinate bilingual communication (English/Korean) with overseas clients, vendors, and contract manufacturers to resolve QA-related inquiries.
• Translate, review, and verify technical documents, packaging specifications, and labeling materials for export compliance.
• Prepare and issue export quality documents such as Product Specifications, Quality Certificates, and Stability Data for Korean regulatory submission.
• Contribute to continuous improvement initiatives in QA workflow and documentation efficiency.

Qualifications:

• Bachelor’s degree in Bioscience, Food Science, Chemistry, or a related discipline
• Minimum of 1–2 years of experience in a QA/QC or manufacturing environment (experience in dietary supplement, food, or pharmaceutical industries preferred)
• Experience in a Korea-based company is a plus
• Strong understanding of Good Manufacturing Practices (GMP) and quality control procedures
• Fluency in both English and Korean (written and verbal) required
• Excellent attention to detail, documentation accuracy, and communication skills

Preferred Qualifications:

• Familiarity with Korean MFDS export documentation and import quality requirements
• Experience collaborating with cross-border teams or international vendors
• Prior experience preparing or reviewing quality certificates, stability reports, or product specifications