Pharma Inspection & Packaging Operator - Flexible Shifts

Inteldot; Manatí (PR); On-site; USD 21,000 - 30,000; Full time

Job summary

Inteldot is seeking an Inspection & Packaging Operator I to perform pharmaceutical product inspection and packaging within a regulated manufacturing environment in Puerto Rico. You will execute manual, semi-automated, and automated inspection, while ensuring cGMP compliance and proper documentation.

The role requires attention to detail, adherence to SOPs, and collaboration with QA, Manufacturing, and Engineering. Previous experience in regulated pharmaceutical settings is preferred.

Qualifications

• High school diploma or GED required; technical education or pharmaceutical manufacturing training preferred.
• Experience in pharmaceutical manufacturing, visual inspection, packaging, or other regulated environments preferred.
• Basic knowledge of cGMP requirements and Good Documentation Practices.

Responsibilities

• Perform visual inspection of pharmaceutical products using manual, semi-automated, or automated inspection methods.
• Operate inspection equipment and computerized systems after qualification.
• Complete batch records and maintain product traceability.
• Identify, classify, and document defects per approved inspection procedures.
• Follow procedures for handling inspected products, samples, and materials.
• Maintain clean, organized, and compliant work areas.

Skills

Attention to detail

Communication skills

Teamwork

SOP adherence

cGMP knowledge

Inspection experience

Packaging operations

Education

High school diploma or GED

Tools

EBR systems

MES

Job description

Inteldot is seeking an Inspection & Packaging Operator I to perform pharmaceutical product inspection and packaging within a regulated manufacturing environment in Puerto Rico. You will execute manual, semi-automated, and automated inspection, while ensuring cGMP compliance and proper documentation.

The role requires attention to detail, adherence to SOPs, and collaboration with QA, Manufacturing, and Engineering. Previous experience in regulated pharmaceutical settings is preferred.