Pharma Material Quality Inspector | GMP & QC

5th HQ; Town of Florida (NY); On-site; USD 23,000 - 28,000; Full time

Benefits offered by this job

Competitive pay

Full-time

Career growth

Supportive team

Job summary

5th HQ in the United States is seeking a Material Quality Inspector to ensure raw materials meet GMP standards before production. The role requires meticulous attention to detail and familiarity with quality control in manufacturing or laboratory settings.

You will collect samples, document results, and collaborate with QC and Production to maintain compliance and efficient workflow. This full-time position offers growth opportunities and a supportive team in a leading pharmaceutical environment.

Qualifications

• Experience in manufacturing, pharmaceutical, or laboratory environment preferred.
• Knowledge of GMP regulations and sampling procedures.
• Strong organizational skills and attention to detail.
• Ability to lift and move raw material containers as needed.
• Basic computer skills to log and track materials.
• Bilingual (English & Spanish) is a plus.

Responsibilities

• Collect raw material samples according to GMP and quality control procedures.
• Label, document, and store samples properly for testing.
• Maintain accurate records of all sampling activities.
• Follow safety protocols and regulatory requirements to prevent contamination.
• Assist in inventory tracking and organization of raw materials.
• Work closely with the Quality Control and Production teams to ensure efficient workflow.
• Perform other duties as assigned.

Skills

Attention to detail

GMP regulations

Documentation

Material handling

Basic computer skills

Bilingual English/Spanish

Job description

5th HQ in the United States is seeking a Material Quality Inspector to ensure raw materials meet GMP standards before production. The role requires meticulous attention to detail and familiarity with quality control in manufacturing or laboratory settings.

You will collect samples, document results, and collaborate with QC and Production to maintain compliance and efficient workflow. This full-time position offers growth opportunities and a supportive team in a leading pharmaceutical environment.