Night Shift Manufacturing Associate (12h)

Amgen Inc. (IR); West Greenwich (RI); On-site; USD 71,000 - 96,000; Full time

Benefits offered by this job

Retirement and Savings Plan

Medical, dental and vision coverage

Life and disability insurance

Flexible spending accounts

Discretionary annual bonus

Job summary

Amgen Inc. is seeking an Associate Manufacturing professional for night shifts to operate in the manufacturing area, adhering to SOPs and drafting technical reports. You will participate in cross-functional teams, own deviations/CAPAs, and implement improvements where needed.

The role emphasizes GMP knowledge, documentation discipline, and collaboration with engineering and quality teams, on a rotating 12-hour schedule with added shift differential.

Qualifications

• High school/GED with manufacturing or operations experience, or an Associate's with relevant time in manufacturing.
• Bachelor's degree in a related field preferred; strong GMP knowledge and analytical capability helps.
• Experience with single-use systems and regulatory CFR knowledge is a plus.

Responsibilities

• Perform operations in the Manufacturing area following SOPs.
• Draft and revise Manufacturing Procedures and technical documents.
• Troubleshoot basic issues and review documentation for assigned functions.
• Collaborate on cross-functional teams and represent manufacturing.
• Possibly own deviations/CAPAs and drive improvements.
• Work on a 12-hour night shift (7PM–7AM) with shift differential.

Skills

Manufacturing experience

Operations experience

Bachelor's degree

Associate’s degree

Education

Bachelor’s degree in Science or Engineering

High school diploma or GED

Associate degree

Tools

DeltaV

Lab equipment

Job description

Amgen Inc. is seeking an Associate Manufacturing professional for night shifts to operate in the manufacturing area, adhering to SOPs and drafting technical reports. You will participate in cross-functional teams, own deviations/CAPAs, and implement improvements where needed.

The role emphasizes GMP knowledge, documentation discipline, and collaboration with engineering and quality teams, on a rotating 12-hour schedule with added shift differential.