Cell Therapy Manufacturing Specialist
South San Francisco, CA, US
Scientific
Bachelors Degree
Full Time, Temporary
35-40/hr
Experienced (Non-Manager)
On-site
Biotechnology/Pharmaceuticals
First Shift (Day)
South San Francisco, CA, US
35-40/hr
Experienced (Non-Manager)
Full Time, Temporary
Biotechnology/Pharmaceuticals
On-site
Scientific
Bachelors Degree
First Shift (Day)
Job details
Cell Therapy Manufacturing Specialist
Kelly® Science & Clinical is seeking a Cell Therapy Manufacturing Specialist for a full-time, 6 month contract position at a cutting-edge client in South San Francisco, CA. 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: $35-38.5/hr AM shifts. $38.5-40/hr for PM shifts
Schedule:
7:00am – 7:30pm?????Sunday – Tuesday; Alternating Wednesday
7:00am – 7:30pm?????Thursday – Saturday; Alternating Wednesday
7:00pm-7:30am??????Sunday – Tuesday; Alternating Wednesday
7:00pm-7:30am??????Thursday – Saturday; Alternating Wednesday
Overview
Our client is an industry-leading company that’s leading the way in advanced cell therapy manufacturing platforms and process sciences. This innovative organization is at the forefront of developing next-generation cell therapy solutions and is growing rapidly within the biotech/biopharma space.
In this role, you will support manufacturing operations and day-to-day lab operations, with hands-on training across Process Development, Analytical Development, and/or MSAT prior to joining the Manufacturing Group. You will execute manufacturing processes in both R&D and GMP environments, contribute to technical presentations, and play a key role in ensuring compliance with established procedures and quality standards.
Responsibilities:
- Perform routine procedures following written instructions, including SOPs, batch records, solution documents, and protocols
- Execute manufacturing processes in both R&D and GMP environments, following protocols and standard operating procedures (SOPs)
- Provide user feedback to engineering and process teams; support requirements gathering and review
- Support reagent preparation, leukopak processing, and sample testing in R&D and GMP environments
- Contribute to the analysis and presentation of technical results at departmental meetings
- Perform routine clean room and laboratory activities including ordering, cleaning, restocking, and equipment qualification/maintenance
- Operate in a controlled GMP environment and perform gowning per procedure
- Complete required training and ensure compliance with established internal and external control procedures
- Assist in the execution of process, equipment, and cleaning validation
- Revise and originate production records, standard operating procedures, protocols, and reports
- Initiate and support the closure of Deviation Reports and CAPAs
- Train and mentor new manufacturing associates on procedures, aseptic techniques, equipment, and troubleshooting skills
- Review in-process and completed documents for accuracy and ensure batch records are submitted to area management within specified timeframes
- Collaborate with Quality Control, Facilities, Materials Management, Quality Assurance, and Validation teams to complete assignments
- Perform other duties as assigned
Qualifications:
- Bachelor’s Degree or diploma in a scientific or related field is required
- 1+ years of experience within the biotech/biopharma industry in cGMP Operations, preferably within cell and gene therapy
- Must know and follow job safety procedures, attend required health and safety training, proactively promote safety at work, and promptly report actual and potential accidents and injuries
- Must comply with the safety policies of the client and site
- Adherence to cGMPs is required at all times during the manufacturing of Cell Therapy products
- Proficiency in Drug Product-related process equipment
- Must have experience following protocols, SOPs, and/or GMP documentation
- Excellent verbal, written, presentation, and interpersonal skills
- Strong analytical and problem-solving skills
- Self-motivated and passionate about advancing the field of cell therapy
- Demonstrates self-awareness, integrity, authenticity, and a growth mindset
- Desire to be part of a rapidly evolving organization, with compelling technology, and take products and processes to the next level
What happens next:
Once you apply, you’ll proceed to next steps if your skills and experience look like a good fit. But don’t worry – even if this position doesn’t work out, you’re still in our network. That means our team of expert Science & Clinical recruiters will have access to your profile, making your opportunities limitless.
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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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