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Cell Manufacturing Specialist Jobs (NOW HIRING)

Bloom Energy

Senior Material Coordinator

Newark, DE · On-site

$61K/yr

From revolutionizing power for AI-driven data centers to ensuring resilience for hospitals, electric grids, manufacturing facilities, and utilities, our solid oxide fuel cell (SOFC) and solid oxide ...

Ultium Cells LLC

... Sr. Specialist - Indirect Material and Spare Parts Permanent Spring Hill, TN, US 8 days ago ... The Ultium cell partners include LG Energy Solutions; the world's largest manufacturer of ...

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Cell Manufacturing Specialist information

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$13

$28

$48

How much do cell manufacturing specialist jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for cell manufacturing specialist in the United States is $28.04, according to ZipRecruiter salary data. Most workers in this role earn between $18.51 and $36.30 per hour, depending on experience, location, and employer.

What is a cell manufacturing specialist?

Cell Manufacturing Specialists are professionals responsible for producing, processing, and ensuring the quality of cells used in medical therapies, such as cell and gene therapies. They work in controlled laboratory or manufacturing environments, following strict protocols to maintain sterility and product integrity. Their daily tasks include preparing cell cultures, monitoring cell growth, performing quality control tests, and documenting each step to comply with regulatory standards. These specialists play a crucial role in advancing regenerative medicine and developing innovative treatments for diseases.

What are the typical daily responsibilities of a cell manufacturing specialist in a biomanufacturing environment?

Cell Manufacturing Specialists are primarily responsible for executing cell culture processes, monitoring bioreactor conditions, and ensuring that all production steps comply with Good Manufacturing Practices (GMP). Their daily tasks often include preparing sterile equipment, handling and expanding cells, performing in-process quality checks, and accurately documenting all activities. They also collaborate closely with quality assurance, process development, and engineering teams to troubleshoot issues and implement process improvements. This role requires strong attention to detail and the ability to work effectively in a highly regulated, team-oriented setting.

What are the key skills and qualifications needed to thrive as a cell manufacturing specialist, and why are they important?

To thrive as a Cell Manufacturing Specialist, you need a solid background in cell biology, laboratory techniques, and a relevant science degree, often supported by experience in cGMP environments. Familiarity with bioreactors, cell culture systems, sterile techniques, and quality control software is typically required, along with certifications such as Good Manufacturing Practice (GMP) training. Attention to detail, problem-solving abilities, and strong teamwork skills help ensure consistent product quality and smooth workflow. These competencies are crucial for maintaining safety, regulatory compliance, and successful production of cell-based therapies.

What are popular job titles related to Cell Manufacturing Specialist jobs?

For Cell Manufacturing Specialist jobs, the most frequently searched job titles are:

Infographic showing various Cell Manufacturing Specialist job openings in the United States as of August 2026, with employment types broken down into 87% Full Time, 11% Part Time, and 2% Contract. Highlights an 78% Physical, 2% Hybrid, and 20% Remote job distribution, with an average salary of $58,318 per year, or $28 per hour.

Manufacturing Operations Specialist (Contract)

Boston, MA • On-site

Vertex Pharmaceuticals
Biotechnology Research and Development • 1 - 5K employees
Learn more about Vertex Pharmaceuticalsexternal

$48 - $52/hr

Other

This job post has expired 1 day ago. Applications are no longer accepted.

Vertex Pharmaceuticals rating

6.5

Company rating: 6.5 out of 10

Based on 5 frontline employees who took The Breakroom Quiz

Job description

Job Description

The Manufacturing Operations Specialist will lead and assist in the day-to-day manufacturing operations at the Leiden Center 1 (LC1) facility. The incumbent will be working in the Clinical Manufacturing facility under a GMP environment supporting aseptic operations inside a BSC and assisting others in various tasks ensuring continuous manufacturing production. The Manufacturing Operations Specialist is a critical hands-on role within Cell Manufacturing. This position is responsible for GMP cell processing operations for adherent and suspension cell cultures. The incumbent will have extreme attention to detail, dedication to patients, and drive to learn and ability to lead a team along with training their peers.This role requires the understanding of and strict adherence to cGMP requirements for cell processing operations involving adherent and suspension cell cultures. The successful candidate will read and interpret Batch Records, SOPs, policies and other relevant work instructions to ensure successful and compliant drug substance manufacturing. In this role, you will also collaborate with Facilities/Operations, Quality, EH&S, Materials Management and related stakeholders to drive efficient manufacturing operations.

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.
Knowledge and Skills
  • Ability to follow verbal and written instructions
  • Minimum 1 year of experience in a GMP environment
  • Minimum 6 months experience with cell culture and demonstration of aseptic technique
  • Basic computer skills Word, Outlook, and equipment interfaces
Education and Experience
  • High School degree and/or 3+ years of experience, or the equivalent combination of education and experience in a related field
  • Ability to follow verbal and written instructions in English
  • Solid communication and documentation skills
Contract Length

12 months with the chance to extend

Pay Range

$48-$52/hr

Shift/Hours

Sunday-Thursday 7am-3:30pm

Requisition Disclaimer

This 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

No C2C or Third-Party Vendors
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