Quality Assurance Inspector - Night Shift

Scorpion Therapeutics; Piscataway Township (NJ); On-site; USD 45,000 - 60,000; Full time

Job summary

Scorpion Therapeutics, based in New Jersey, is seeking a QA Inspector to sample, inspect, and test raw materials, packaging components, and finished products to ensure GMP compliance.

The role entails inspecting incoming materials, performing in-process and final quality checks, managing labeling components, and maintaining meticulous records in a contained biopharma manufacturing environment. 12-hour rotating shifts 6:00 PM–6:30 AM, including every other weekend.

Qualifications

• High School diploma or GED required.
• At least 1 year in QA or related field.
• Strong attention to detail and good math skills.

Responsibilities

• Inspect incoming materials
• Conduct in-process and final quality checks
• Manage labeling components
• Maintain detailed records
• Ensure environmental and facility compliance during manufacturing and packaging

Skills

Attention to detail

Math skills

Record-keeping

Education

High School diploma or GED

Tools

Lab equipment calibration

Job description

Role

QA Inspector responsible for sampling, inspection, and testing of raw materials, packaging components, and finished products to ensure compliance with GMP standards.

Responsibilities

• Inspect incoming materials
• Conduct in-process and final quality checks
• Manage labeling components
• Maintain detailed records
• Ensure environmental and facility compliance during manufacturing and packaging

Requirements

• High School diploma or GED
• 1+ year in QA or related field
• Strong attention to detail
• Good math skills
• Record-keeping abilities

Preferred qualifications

Preferred qualifications are not explicitly stated.

High Value

• Role involves GMP compliance, microbiological and chemical testing
• Calibration of lab equipment
• Working within a contained manufacturing environment

Shift

12-hour rotating shift from 6:00 PM to 6:30 AM, including every other weekend.

Scope

No specific therapeutic areas, modalities, or development stages are indicated, focusing primarily on manufacturing quality assurance within a biopharma setting.