Associate Manufacturing - West Greenwich RI

VetJobs; West Greenwich (RI); On-site; USD 75,000 - 100,000; Full time

Job summary

Amgen West Greenwich, Rhode Island, is seeking an Associate Manufacturing - Days (A Shift) to perform buffer and media operations per SOPs, monitor critical processes, and draft technical reports.

You will participate in cross-functional teams, perform routine validation protocols, and review documentation. The role may own minor deviations and drive improvements while adhering to GMP and CFR guidelines in a manufacturing setting.

Qualifications

• High school/GED required with 2 years of manufacturing or operations experience, or an Associate’s or Bachelor's degree.
• GMP processing knowledge and CFR familiarity.
• Experience with DeltaV and lab equipment/testing.
• Ability to write technical documents and SOPs.
• Strong collaborative skills for cross-functional teams.

Responsibilities

• Perform operations in Buffer and Media processes per SOPs.
• Monitor critical processes and execute validation protocols.
• Draft and revise Manufacturing Procedures, SOPs, and technical reports.
• Troubleshoot basic issues and review documentation.
• Collaborate on cross-functional teams and drive improvements.

Skills

GMP knowledge

DeltaV

LIMS access

Technical writing

Statistical skills

Troubleshooting

Cross-functional collaboration

Education

High School/GED

Tools

TrackWise

LIMS

Job description

Job Description

ATTENTION MILITARY AFFILIATED JOB SEEKERS. Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. Unless specifically stated otherwise, this role is "On-Site" at the location detailed in the job post.

Associate Manufacturing - Days (A Shift)

What you will do

Let’s do this. Let’s change the world. In this vital role you will perform operations in the Manufacturing area, specifically Buffer and Media processes. Operations will be performed according to Standard Operating Procedures (SOPs). Associate will perform and monitor critical processes, execute routine validation protocols, and regularly draft and revise documents such as Manufacturing Procedures, SOPs, and technical reports. Associate will also perform basic troubleshooting and assist in the review of documentation for assigned functions. May participate on cross-functional teams and represent the Solutions Prep group. Associate may also have the responsibility of owning minor deviations. In addition, Associate may identify, recommend, and implement improvements related to routine functions.

What we expect of you

We are all different, yet we all use our outstanding contributions to serve patients. The hard‑working professional we seek is a committed team player with these qualifications.

Auto req ID

482538BR

Minimum Education Required

High School/GED

Basic Qualifications

• High school/GED + 2 years of manufacturing or operations work experience OR
• Associate’s + 6 months of manufacturing or operations work experience OR
• Bachelor’s

Preferred Qualifications

• Knowledge of large-scale Buffer and Media operations, GMP processing, etc.
• CFR and Regulatory knowledge
• Mechanical ability/expertise
• Knowledge of WIP lab equipment and computers, with LIMS access
• Basic statistical mathematical skills
• Ability to interpret and apply GMP knowledge
• Ability to demonstrate technical writing capability with Trackwise access
• Independently collaborate with support groups.
• Ability to understand, apply and evaluate basic chemistry, biology and physical principles
• Basic troubleshooting skills on Buffer and Media equipment
• Experience with Delta V.
• Experience with lab equipment/testing

Salary Range

70,985.20USD -96,038.80 USD

$75,000-$100,000

City

West Greenwich

State

Rhode Island

Job Category

Scientific Research & Development

Job Code

Pharmaceutical Pharmaceutical

Affiliate Sponsor

Amgen