Manufacturing Specialist

Kelly Science, Engineering, Technology & Telecom; Greensboro, Winston-Salem, High Point (NC, NC, NC); On-site; USD 38,572 - 42,705; Full time

Job summary

A leading biotech organization in Greensboro is seeking a Manufacturing Cell Processing Specialist II to be part of their innovative cell therapy manufacturing team. This role involves leading critical cell processing activities in a cGMP environment, employing aseptic techniques, and mentoring team members. Candidates should have 2–4+ years of relevant experience and a degree in a related field. This opportunity offers exposure to advanced technologies and a chance to make a meaningful patient impact.

Qualifications

• 2–4+ years of experience in cell therapy, biotech, or biologics manufacturing.
• Direct experience working in a cGMP-regulated cleanroom environment.
• Strong understanding of aseptic technique and controlled documentation practices.

Responsibilities

• Lead and execute critical cell processing activities in a cGMP environment.
• Perform aseptic manufacturing in cleanroom settings, applying sterile technique.
• Mentor team members and contribute to building a quality-focused manufacturing culture.

Skills

Aseptic manufacturing

Problem-solving

Communication skills

Education

AS or BS in Biotechnology, Biology, Chemistry, or related field

Tools

ERP systems

Job description

Manufacturing Cell Processing Specialist II (Contract)

🧬 Advanced Cell Therapy Manufacturing

Hourly Pay Rate: $28-$31

Are you ready to be part of cutting-edge cell therapy manufacturing that is transforming the future of medicine? We are seeking a Manufacturing Cell Processing Specialist II to join a fast-growing, innovative biotech organization focused on advanced cellular therapies. This is an exciting opportunity to work in a highly collaborative, mission-driven environment where your expertise directly impacts life‑changing therapies.

This onsite contract role offers hands‑on involvement in GMP-regulated manufacturing, cleanroom operations, and advanced cell processing technologies.

What You’ll Do

• Lead and execute critical cell processing activities in a cGMP environment.
• Perform aseptic manufacturing in cleanroom settings, applying sterile technique and regulatory best practices.
• Operate and troubleshoot specialized production equipment, including controlled‑rate freezers and orbital shakers.
• Execute final product freezing and LN2 storage with strict adherence to quality standards.
• Own and review GMP documentation including batch records, logbooks, and SOPs in alignment with GDP requirements.
• Support and lead deviation investigations and CAPA activities to drive continuous improvement.
• Mentor team members and contribute to building a strong, quality‑focused manufacturing culture.
• Assist with process validation, material qualification, and data analysis initiatives.

What We’re Looking For

• AS or BS in Biotechnology, Biology, Chemistry, or related field (or equivalent experience).
• 2–4+ years of experience in cell therapy, biotech, or biologics manufacturing.
• Direct experience working in a cGMP-regulated cleanroom environment.
• Strong understanding of aseptic technique and controlled documentation practices.
• Experience with ERP systems and electronic batch documentation preferred.
• A proactive mindset with strong problem‑solving and communication skills.

Why This Role Stands Out

• Work at the forefront of advanced cellular therapy manufacturing.
• Be part of a high‑growth biotech environment with meaningful patient impact.
• Gain exposure to innovative technologies and scalable manufacturing processes.
• Collaborate with a passionate, quality‑driven team focused on excellence and compliance.

If you’re looking for a hands‑on role in a fast‑paced biotech manufacturing setting where your work truly matters, this is an opportunity worth exploring.