Manufacturing Specialist 3rd shift (Contract)

Vertex Pharmaceuticals LLC; Boston (MA); Sur place; USD 63 000 - 69 000; Plein temps

Résumé du poste

Vertex Pharmaceuticals LLC is seeking a Manufacturing Operations Associate to support the production of clinical cell therapy products in a cGMP environment. The role involves aseptic processing, raw material preparation, batch record execution, and cleanroom operations to ensure high-quality product output, with a strong emphasis on quality and cross-functional collaboration.

This 12-month contract is on a 3rd shift (9pm–7:30am) and requires 4–6 years of manufacturing experience.

Qualifications

• 4–6 years manufacturing experience required.

Responsabilités

• Perform clinical product manufacturing for cell therapy per cGMP standards.
• Assemble raw materials and follow SOPs for manufacturing.
• Complete batch records and review MBRs the same day of execution.
• Coordinate with QA Document Control for MBRs and deviations.
• Support Operations to ensure proper resource availability and compliance.

Connaissances

Aseptic processing

Batch records

cGMP manufacturing

SOP adherence

Cleanroom operations

Deviations reporting

Description du poste

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 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 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.

Shift/Hours

9pm - 7:30AM, Sunday-Wed or Wed-Saturday.