Associate Manufacturing - Solution Prep (Nights)

Scorpion Therapeutics; West Greenwich (RI); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Night shift differential

Job summary

Amgen is seeking an Associate Manufacturing Night shift operator at a Rhode Island biotech facility. You will perform GMP-compliant batch operations of solutions, buffers and media, and work onsite during night shifts.

The role requires a high school diploma/GED with manufacturing experience or an advanced degree, and familiarity with purification, cell culture, aseptic techniques, plus knowledge of GMP/CFR standards. Collaboration with quality and technical teams is essential.

Qualifications

• High school diploma or GED with 2 years manufacturing experience.
• Associate degree with 6 months' experience or a Bachelor's in Science/Engineering.
• Familiarity with biotech processes and regulatory standards (GMP, CFR).

Responsibilities

• Execute batching and transfer processes.
• Monitor critical procedures.
• Draft and revise manufacturing documentation.
• Troubleshoot basic issues.
• Support quality and process improvements.

Skills

GMP compliance

Troubleshooting

Documentation

Biotech processes

Education

High school diploma/GED

Associate degree

Bachelor's in Science/Engineering

Tools

Delta V

Single-use-Systems

Job description

Role: Associate Manufacturing Night shift operator at Amgen's biotech facility, primarily performing GMP-compliant batch operations of solutions, including buffers and media, within a biologics manufacturing environment.

Responsibilities:

• Execute batching and transfer processes
• Monitor critical procedures
• Draft and revise manufacturing documentation
• Troubleshoot basic issues
• Support quality and process improvements

Requirements:

• High school diploma/GED plus 2 years of manufacturing experience, or associate's degree plus 6 months' experience, or bachelor’s in Science/Engineering
• Familiarity with biotech processes like purification, cell culture, aseptic techniques
• Knowledge of GMP, CFR, and regulatory standards
• Basic statistical and troubleshooting skills

Preferred:

• Experience with large-scale biotech operations, Single-use-Systems, Delta V, analytical methods, technical writing, project management, and physical/chemical principles

High-Value:

Biologics manufacturing, GMP compliance, night shift schedule with 12-hour rotations, including a 15% shift differential; working at a state-of-the-art biologics facility advancing medicines for serious illnesses across oncology, inflammation, rare diseases, and other therapeutic areas. Collaboration with manufacturing, quality, and technical teams. The role does not specify travel or remote work, but involves working onsite during night shifts.