Associate Quality Control - Nights

Scorpion Therapeutics; West Greenwich (RI); On-site; USD 60,000 - 90,000; Full time

Job summary

Amgen seeks an Associate Quality Control professional for the night shift to perform GMP analytical testing in a biopharma setting. You will handle assays on manufacturing samples, raw materials, and environmental monitoring, while ensuring compliance with GMP standards.

The role requires experience in analytical/biological testing, familiarity with QC systems, and strong organizational and communication skills to support investigations and documentation.

Qualifications

• Requires a high school diploma or GED with 2+ years of experience, or an associate's/bachelor's degree.
• 1–3 years GMP lab experience.
• Proficiency in analytical/biological testing per Methods/Compendia.
• Familiarity with QC systems.
• Strong organizational, communication, and analytical skills.
• Understanding of biopharma processes.

Responsibilities

• Perform assays on manufacturing samples (e.g., Titer, Endotoxin, Microbiology), raw materials, environmental monitoring, and utilities.
• Ensure compliance with GMP, GDP, safety, and regulatory standards.
• Generate and review documentation.
• Operate laboratory equipment.
• Support troubleshooting, deviations, and investigations.

Skills

GMP lab experience

Analytical testing

Biological testing

QC systems

Organizational skills

Communication skills

Analytical skills

Biopharma processes

Biopharma investigations

QC procedures

Education

High school diploma/GED

Associate's degree

Bachelor's degree

Job description

Role

Associate Quality Control (Night Shift) at Amgen, supporting GMP analytical testing in a biopharma environment.

Responsibilities

• perform assays on manufacturing samples (e.g., Titer, Endotoxin, Microbiology), raw materials, environmental monitoring, and utilities
• ensure compliance with GMP, GDP, safety, and regulatory standards
• generate and review documentation
• operate laboratory equipment
• support troubleshooting, deviations, and investigations

Requirements

• high school diploma/GED with 2+ years, associate's degree with 6+ months, or bachelor's degree
• 1-3 years GMP lab experience
• proficiency in analytical/biological testing per Methods/Compendia
• familiarity with QC systems
• strong organizational, communication, and analytical skills
• understanding of biopharma processes

Preferred

• experience with biopharmaceuticals, investigations, and QC procedures

High Value

• GMP analytical lab, biopharmaceuticals, night shift (Tuesday-Friday, 10 PM-8 AM), environmental and raw material testing, troubleshooting, documentation, and compliance

Work Setup

• on-site in Rhode Island