Night-Shift Manufacturing Associate – GMP & Biotech Ops

BioSpace; West Greenwich (RI); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Retirement & Savings Plan

Medical/Dental/Vision coverage

Life & Disability Insurance

Flexible Spending Accounts

Flexible work model

Job summary

Amgen is seeking an Associate Manufacturing - Nights in Rhode Island. You will perform 12-hour shift operations in the manufacturing area, handling buffers and media per SOPs, while applying GMP and documenting in batch records.

You will monitor processes, help draft procedures, and support deviation handling, LEAN initiatives, and continuous improvements. Qualified candidates bring a 2-year manufacturing OR higher, with knowledge of GMP, DeltaV, and lab techniques; a related Bachelor's degree

Qualifications

• High school/GED + 2 years manufacturing or operations experience OR
• Associates + 6 months manufacturing or operations experience OR
• Bachelor's degree in a related field

Responsibilities

• Perform batching and transfer of Buffers and Media per SOPs.
• Follow and monitor critical processes; draft and revise Manufacturing Procedures and SOPs.
• Conduct basic troubleshooting and assist in documentation reviews for functions.
• Initiate and own area Deviations; revise SOPs and perform LEAN functions.
• Identify, recommend, and implement routine function improvements.

Skills

Biotech operations knowledge

GMP knowledge

Single-use Systems

CFR & Regulatory knowledge

Mechanical ability

Statistical math

Technical writing

Project management

Analytical chemistry/biology basics

Troubleshooting equipment

DeltaV experience

Lab equipment/testing

Education

Bachelor's degree in related field

Bachelor's degree in Science or Engineering

Tools

DeltaV

Job description

Amgen is seeking an Associate Manufacturing - Nights in Rhode Island. You will perform 12-hour shift operations in the manufacturing area, handling buffers and media per SOPs, while applying GMP and documenting in batch records.

You will monitor processes, help draft procedures, and support deviation handling, LEAN initiatives, and continuous improvements. Qualified candidates bring a 2-year manufacturing OR higher, with knowledge of GMP, DeltaV, and lab techniques; a related Bachelor's degree