QC Incoming Inspector – Packaging & Materials QA

Johnson & Johnson Co.; Gurabo (PR); On-site; USD 42,000 - 54,000; Full time

Job summary

Johnson & Johnson in Gurabo, Puerto Rico, United States is seeking a Quality Incoming Inspector to sample, inspect, and approve packaging components and raw materials to ensure timely release and supply chain integrity. The role emphasizes adherence to GMP, documentation discipline, and cross-functional collaboration.

The ideal candidate will have a Natural Science background with GMP experience, fluency in Spanish and English, and ability to work 1st–3rd shifts, including overtime and weekends,

Qualifications

• Bachelor’s degree in Natural Science (Biology or Chemistry) with 0–2 years GMP experience, or Associate’s degree with 2–4 years GMP, or HS diploma with 4+ years GMP.
• Knowledge of cGMPs and safety regulations required.
• Fluent in Spanish and English; basic computer skills and word processing.

Responsibilities

• Performs sampling, inspection, testing, and approval of packaging components per regulations and policies.
• Performs sampling and testing of raw materials to meet cycle time goals.
• Inspects labeling, quantity, and materials for shipment.
• Maintains Retention Room and documents in safe files.

Skills

Analytical reasoning

Business behavior

Compliance management

Continuous improvement

Controls compliance

Data analysis

Execution focus

ISO 9001

Persistence and tenacity

Quality control (QC)

Quality control testing

Quality standards

Quality systems documentation

Report writing

Sample testing

Technologically savvy

Education

Bachelor’s Degree in Natural Science (Biology or Chemistry)

Associate’s Degree in Natural Science

High School Diploma with 4+ years GMP experience

Job description

Johnson & Johnson in Gurabo, Puerto Rico, United States is seeking a Quality Incoming Inspector to sample, inspect, and approve packaging components and raw materials to ensure timely release and supply chain integrity. The role emphasizes adherence to GMP, documentation discipline, and cross-functional collaboration.

The ideal candidate will have a Natural Science background with GMP experience, fluency in Spanish and English, and ability to work 1st–3rd shifts, including overtime and weekends,