Kelly® Science & Clinical is seeking an Immunotherapy Manufacturing Associate for a contract-to-hire opportunity with one of our clients, a commercial-stage biotechnology company in the Los Angeles, CA area. If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.
Pay rate: $22,05/hour +  $5/hour shift differential
Workplace: Onsite in the Los Angeles, CA area
Training and Work Schedule:

• Week 1
  

  • Monday 9am – 5pm:  NEO TRAINING
    

  • Tue – Thurs: 12:30 – 23:00
    

  
  

• Week 2 (4×10)
  

  • Mon – Thurs: 12:30 – 23:00
    

  
  

• Week 3 (4×10)
  

  • Mon – Thurs: 12:30 – 23:00
    

  
  

• Week 4 (3×12)
  

  • Wed – Fri: 14:30 – 03:00
    

  
  

• Week 5 (3×12)
  

  • Wed – Fri: 14:30 – 03:00
    

  
  

• Week 6 – 10 (4×10)
  

  • Mon – Tues: 18:30 – 05:00
    

  • Wed – Thurs: 16:30 – 03:00
    

  
  

• Week 11 and beyond
  

  • Begin Split Shift (3×12)
    

  • Mon, Tue, Fri:  19:30 – 08:00
    

Overview
Join a pioneering biopharmaceutical organization at the forefront of personalizing cancer treatment. We develop and manufacture cutting-edge immunotherapies that harness a patient’s own immune system to fight cancer. Our breakthrough therapies, manufactured using advanced cell processing and aseptic techniques, represent the next generation of individualized medicine.
With state-of-the-art Immunotherapy Manufacturing Facilities located in Seal Beach, CA, and a collaborative team of industry leaders across the country, we are dedicated to transforming lives through scientific excellence and innovation.
Overview
As an Immunotherapy Manufacturing Associate, you will play a critical role in manufacturing and assembling advanced biologics in a highly controlled cleanroom environment (Class 10,000/ISO7 and Class 100,000/ISO8). This is an impactful, hands-on opportunity to support life-changing therapies for patients with cancer.
What You’ll Do

• Accurately weigh, measure, and verify raw materials to ensure product quality and compliance.
  

• Maintain meticulous records, supporting regulatory standards and driving continuous improvements to manufacturing documentation.
  

• Execute aseptic processing of cellular therapies using Standard Operating Procedures and strict GMP guidelines.
  

• Collaborate with a multidisciplinary team on projects and GxP-compliance initiatives.
  

• Manage shipping logistics—preparing and documenting outbound and inbound materials.
  

• Examine and stock both GMP and non-GMP materials, ensuring operational excellence.
  

• Flexibly support all operational functions and respond to shifting priorities as business needs evolve.
  

• Contribute to process improvement and cross-functional team projects.

Qualifications

• High school diploma with 3–5 years of consistent work experience OR an Associate’s/Technical degree.
  

• Recent graduates with a BA/BS in Science are encouraged to apply; prior industry experience is a plus but not required.
  

• Experience in biotech, pharma, or medical device manufacturing preferred.
  

• Strong proficiency with quality and compliance documentation.
  

• Excellent English communication skills, both verbal and written.

Your Impact
If you thrive in a fast-paced, innovative environment and are passionate about advancing immunotherapy manufacturing in the Los Angeles area, we invite you to make a difference with us. Your dedication will contribute directly to bringing breakthrough cancer treatments to patients who need them most.

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