Manufacturing Specialist 3rd shift
Listed on 2026-10-11
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Manufacturing / Production
Pharmaceutical Manufacturing, Manufacturing & Industrial Operations, Production Associate / Production Line, Production QC/QA
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
Tuesday-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
- 4 - 6 years manufacturing experience is required.
$46/hr.
- $50/hr.
9pm - 7:30AM, Sunday-Wed or Wed-Saturday.
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