Manufacturing Specialist 3rd shift
Listed on 2026-09-20
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Manufacturing / Production
Pharmaceutical Manufacturing, Manufacturing & Industrial Operations, Production Associate / Production Line
Job Description
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.
Key Duties and 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, repo1ting 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 cleamoom environment.
- Perform M 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 assign
Required Experience & Education
- 4 - 6 years manufacturing experience is required.
Contract Length: 12-month contract with a chance to extend.
Pay Range$46/hr.
- $50/hr.
9pm - 7:30AM, Sunday-Wed or Wed-Saturday.
Requisition DisclaimerThis job posting is for a temporary role with a third-party agency partner on assignment at Vertex Pharmaceuticals Vertex . 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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