Cell Therapy Manufacturing Specialist

Job Description

Job Description

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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As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

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.

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