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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.

Key Duties and Responsibilities

•  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, and reporting deviations
•  Demonstrates and assists others with aseptic technique
•  May participate in technology transfer and final process development from the Development to the Manufacturing group - Occasionally supports the development of Standard Operating Procedures (SOPs) or other documentation for manufacturing in collaboration with Development and Quality groups.
•  Ensures raw materials are identified and available in time for manufacturing activities - Transfer raw material inside cleanroom suite using sanitizing reagents
•  Supports 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 to meet departmental requirements
•  Works in a cleanroom and office setting
•  Must be able to remain in a stationary position 50% during processing activities
•  Frequently move about inside the cleanroom to accomplish process tasks
•  Occasionally moves lab equipment and materials weighing up to 50 pounds
•  Compressed gasses and LN2 are used in this process

Required Experience & Education

• 2-4 years manufacturing experience is required.

Contract Length: 6-month contract with a chance to extend. 

$42-$48/HR

This job posting is for a is for a temporary role with a third-party agency partner on assignment at Vertex Pharmaceuticals.  The individual selected for this role will be offered the role as an employee of a third-party agency partner; compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by the third-party agency partner upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors, including skills, competencies, experience, location and/or being pursued and other job-related factors permitted by law. In addition, this role will be eligible for overtime pay, in accordance with federal and state requirements

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If you do not agree with the Atrium Terms and Conditions, you can still complete your application for this position by emailing your resume to our team at tempstaffing@vrtx.com. Please include the job title in the subject of your email.

No C2C or Third-Party Vendors