Night Shift Manufacturing Technician – Make a Patient Impact

Biopharma Careers; West Greenwich (RI); On-site; USD 54,000 - 74,000; Full time

Benefits offered by this job

Total Rewards Plan

Stock-based incentives

Flexible work models

Job summary

Amgen is seeking a Manufacturing Process Technician - Nights to perform bulk manufacturing steps in aseptic and non-aseptic environments. The role operates within a 12-hour night shift, with a 7am-7pm rotation schedule and a 15% shift differential, following SOPs and batch records for accurate processing.

Expect to join a dynamic team focused on delivering medicines for cancer and other serious diseases, while adhering to cGMP, safety, and quality standards and contributing to continuous

Qualifications

• High school/GED + 1 year of Manufacturing or Operations work or military experience OR
• Associate's degree

Responsibilities

• Equipment and parts cleaning using manual and automated methods and equipment
• Set up and breakdown of single use materials
• Weigh and dispense of raw materials
• Operation and process monitoring of clean systems, autoclaves, and processing equipment
• Sample collection, processing, storage and delivery
• Product and component reconciliation
• Solution preparation and transfer
• Materials handling, weighing and dispensing, power industrial vehicle operation
• Strict adherence to current Good Manufacturing Practices (cGMP's), responsible to accurately complete process-associated documentation, make calculations and perform the physical tasks associated with bulk manufacturing and other duties as assigned.

Skills

cGMP knowledge

Quality-minded

Team collaboration

Attention to detail

Strong communication

Basic math

Education

High school diploma or GED

Associate's degree

Job description

Amgen is seeking a Manufacturing Process Technician - Nights to perform bulk manufacturing steps in aseptic and non-aseptic environments. The role operates within a 12-hour night shift, with a 7am-7pm rotation schedule and a 15% shift differential, following SOPs and batch records for accurate processing.

Expect to join a dynamic team focused on delivering medicines for cancer and other serious diseases, while adhering to cGMP, safety, and quality standards and contributing to continuous