Description
Manufacturing Cell Processing Specialist II (Contract)
Location: Winston-Salem, NC | Onsite
Pay Rate: $28-$31
The Manufacturing Cell Processing Specialist II plays a key role in supporting advanced cell therapy manufacturing operations in a cGMP-regulated environment. This position focuses on hands-on cell processing activities, operating specialized production equipment, and ensuring compliance with established manufacturing and quality standards.
The role also contributes to process improvement initiatives, supports investigations, and provides mentorship to team members while maintaining a strong focus on safety, documentation accuracy, and product quality.
Please note: This is a contract position and benefits are not included.
Responsibilities-
Lead and support cell processing activities in accordance with cGMP guidelines and manufacturing procedures.
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Read, understand, and execute Standard Operating Procedures (SOPs) for assigned tasks while providing guidance to team members as needed.
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Set up, operate, and troubleshoot manufacturing equipment such as controlled-rate freezers, orbital shakers, and related production systems.
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Perform final product freezing and storage of cell therapy materials in LN2 while maintaining strict quality standards.
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Maintain and update SOPs, batch records, and manufacturing documentation to ensure GMP compliance.
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Conduct routine inventory cycle counts and maintain accurate material tracking.
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Execute ERP transactions including material requests and production documentation.
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Ensure accuracy of GMP documentation such as batch records, logbooks, and forms in accordance with Good Documentation Practices (GDP).
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Support and lead deviation investigations and CAPA activities when necessary.
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Provide mentorship and training to junior staff on cell processing techniques and cGMP compliance.
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Drive continuous improvement initiatives and support incident investigations and resolution efforts.
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Perform aseptic manufacturing operations in a cleanroom environment while adhering to sterile technique and regulatory standards.
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Conduct material qualification testing for incoming manufacturing materials.
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Support process development and validation activities as needed.
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Assist with data collection, analysis, and reporting for process optimization.
Education
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Associate or Bachelor's degree in Biotechnology, Biology, Chemistry, or a related scientific field preferred.
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Equivalent relevant experience may substitute for formal education.
Experience
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2–4 years of experience in cell processing, biotechnology manufacturing, or related laboratory/manufacturing environment.
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At least 1–2 years of experience working in a cGMP-regulated environment preferred.
Skills
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Strong understanding of cGMP requirements and documentation practices.
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Experience working in cleanroom and aseptic processing environments.
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Proficiency with Microsoft Office and ERP systems preferred.
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Excellent organizational, documentation, and time management skills.
Additional Attributes
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Strong problem-solving abilities and attention to detail.
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Effective written and verbal communication skills.
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Collaborative team mindset with a commitment to quality and compliance.
As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.
Why Kelly® Science & Clinical?
Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world's most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals—it's the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.About Kelly
Work changes everything. And at Kelly, we're obsessed with where it can take you. To us, it's about more than simply accepting your next job opportunity. It's the fuel that powers every next step of your life. It's the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life—just ask the 300,000 people we employ each year.Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
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