×
Register Here to Apply for Jobs or Post Jobs. X

Manufacturing Specialist

Job in High Point, Guilford County, North Carolina, 27264, USA
Listing for: Kelly Science, Engineering, Technology & Telecom
Full Time position
Listed on 2026-06-26
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Production QC/QA, Validation Engineer
Salary/Wage Range or Industry Benchmark: 28 - 31 USD Hourly USD 28.00 31.00 HOUR
Job Description & How to Apply Below

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.

#J-18808-Ljbffr
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary