Manufacturing Specialist 3rd shift (Contract)

Vertex Pharmaceuticals•Boston, MA

2d•$46 - $50•Onsite

About The Position

We are looking for a motivated and detail-oriented Manufacturing Operations Associate to support the production of clinical cell therapy products in a cGMP manufacturing environment. In this hands-on role, you will perform critical manufacturing activities including aseptic processing, raw material preparation, batch record execution, and cleanroom operations to ensure the consistent production of high-quality cell therapy products. The ideal candidate will have prior manufacturing experience in a regulated environment, a strong commitment to quality and compliance, and a collaborative mindset to support cross-functional teams in advancing innovative cell therapy programs. This position offers the opportunity to play a direct role in delivering life-changing therapies while working in a fast-paced and highly collaborative manufacturing setting. This will be 3rd shift. 9pm - 7:30AM Sunday-Wed or Wed-Saturday. Will train on 1st or 2nd shift for 60ish days.

Requirements

4 - 6 years manufacturing experience is required.
cGMP manufacturing environment experience
Aseptic processing experience
Raw material preparation experience
Batch record execution experience
Cleanroom operations experience
Strong commitment to quality and compliance
Collaborative mindset

Responsibilities

Complete an accelerated onboarding within Manufacturing, learning program processes.
Perform clinical product manufacturing for cell therapy according to cGMP standards. Includes assembling raw materials, following specific standard operating procedures (SOP), aseptic technique, completing batch records, reporting deviations.
Follow Standard Operating Procedures (SOPs) for manufacturing.
Contribute to technical projects both hands-on and documentation
Perform as SME in the role
Perform weigh and dispense activities in cleanroom environment.
Perform MBR review on manufacturing executed documents on the same day of execution.
Work with QA Document Control to request, receive, and return MBRs for process operations.
Ensures raw materials are identified and available in time for manufacturing activities
Support Operations group to ensure proper coordination of resources
Ensures cGMP compliance through consistent execution
Demonstrate the Vertex Phenotype behaviors: Lead by Example; Learn, Teach & Develop; Foster Exceptional Collaboration; Drive Breakthrough Results; and Promote Enterprise Thinking.
Other duties and projects as assigned