Biomanufacturing Specialist

Mykelly; Houston (TX); On-site; USD 50,000 - 55,000; Full time

Job summary

Mykelly is recruiting a Manufacturing Specialist for a premier biotechnology organization in Houston, TX. This role operates in a GMP-regulated environment focused on biopharmaceutical production, preclinical and clinical programs, and advancing gene therapy research.

You will operate manual, semi-automated, and automated equipment for production of biopharmaceuticals, conduct large-scale cell culture, and assist with viral vector purification while maintaining rigorous documentation.

Qualifications

• Bachelor’s degree in Biology, Biotechnology, or related field.
• Experience in GMP-regulated biopharmaceutical manufacturing.
• Experience with cell culture, chromatography, and aseptic processing.
• Strong documentation and CAPA/quality systems understanding.

Responsibilities

• Operate manual, semi-automated, and automated equipment for production of biopharmaceuticals.
• Perform large-scale cell culture with single-use bioreactor systems.
• Contribute to viral vector purification using process-scale chromatography equipment.
• Prepare buffers and staging materials; maintain cleanroom documentation.
• Assist validation, data collection, inventory, and equipment maintenance.
• Write/review SOPs and change controls; participate in safety programs.

Skills

GMP experience

Bioprocessing knowledge

Documentation proficiency

Team collaboration

Education

Bachelor’s degree in Biology, Biotechnology, or related field

Job description

Think the best job opportunities are far away? Think again. Great opportunities are right here in your backyard. Kelly® is looking for a Manufacturing Specialist to work at a premier biotechnology organization in Houston, TX. Let us help you grow at work and discover the next step in your career, all while being a vital part of your community.

Pay Rate: $36-40/hour

Shift: Mon-Fri | 8:00am–4:30pm

Why you should apply to be a Manufacturing Specialist:

• Competitive pay rate with weekly pay options
  
• Opportunity to support groundbreaking gene therapy research and production
  
• Safe, clean, GMP-regulated manufacturing environment
  
• Work with cutting-edge bioprocessing technology and equipment
  
• Collaborative workplace culture with opportunities for skill development and advancement

What’s a typical day as a Manufacturing Specialist? You’ll be:

• Operating manual, semi-automated, and automated equipment for the production of preclinical and clinical biopharmaceuticals
  
• Performing large-scale cell culture with single-use disposable bioreactor systems
  
• Conducting viral vector purification using process-scale chromatography equipment
  
• Preparing buffer solutions and staging equipment/raw materials in production suites
  
• Assisting with validation, data collection, inventory management, and equipment maintenance
  
• Cleaning facility and unit process equipment, and ensuring completion of proper documentation to meet quality system requirements
  
• Writing and reviewing SOPs and change control documents for manufacturing work areas
  
• Participating in facility safety programs and resolving technical problems with internal teams and external vendors

This job might be an outstanding fit if you:

• Have a Bachelor’s degree in Biology, Biotechnology, or a related scientific field (required)
  
• Bring experience in biopharmaceutical manufacturing, ideally in a GMP-regulated environment (preferred but not required)
  
• Are skilled in upstream and/or downstream manufacturing processes, including cell culture, aseptic processing, biosafety cabinets, process-scale chromatography, buffer preparation, and viral vector manufacturing/purification
  
• Demonstrate understanding of cGMP requirements, deviation investigations, root cause analysis, CAPAs, and quality systems
  
• Have strong aseptic technique, attention to contamination control, and commitment to accurate documentation
  
• Are comfortable performing repetitive laboratory/manufacturing tasks and following written procedures
  
• Communicate and collaborate effectively across departments and levels
  
• Can troubleshoot routine technical issues and elevate appropriately
  
• Are physically able to work in a GMP cleanroom environment, follow gowning requirements, lift up to 50 lbs. with assistance, and consistently adhere to safety and environmental procedures