Manufacturing Associate, Cell Therapy
Kelly® Science & Clinical is seeking a Manufacturing Associate for 6-month contract position with a national CDMO leader at their site 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.
Compensation: Day Shift: $35.00-38.00, Night Shift: $38.00-40.00
Schedule: 4 options, (12-hour shifts)
7:00 - 19:30?????Sunday - Tuesday; Alternating Wednesday
7:00 - 19:30?????Thursday - Saturday; Alternating Wednesday
19:00-7:30??????Sunday - Tuesday; Alternating Wednesday
19:00-7:30??????Thursday - Saturday; Alternating Wednesday
Location : South San Francisco, CA
Duration : 6-month contract
SUMMARY
We are seeking an innovative and highly motivated Cell Therapy Manufacturing Associate to
join our Process Sciences team who will contribute significantly to the development and
manufacture of our advanced cell therapy manufacturing platform. The primary focus of this
position will be to support manufacturing operations, as well as day-to-day lab operations. This
is a hands-on position that will train in Process Development, Analytical Development, and/or
MSAT prior to joining the Manufacturing Group.
Candidates should enjoy working in a fast-paced, mission-driven environment, and be
prepared to tackle a broad selection of challenges as the company grows.
RESPONSIBILITIES
Perform routine procedures following written instructions (SOPs, batch records, solution documents, protocols, etc.)
Execute manufacturing processes in both an R&D and GMP environments, following protocols and/or standard operating procedures (SOPs)
Provide user feedback to engineering and process teams, support with requirements gathering and review
Support reagent preparation, leukopak processing, and sample testing in an R&D and GMP environment
Contribute to 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 as 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
Responsible for revising and originating 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 trouble-shooting skills
Review in-process and completed documents for accuracy and to make sure batch records are turned in to area management within specified days of completion
Work with Quality Control, Facilities, Materials Management, Quality Assurance and
Validation to complete assignments
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 company 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
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 levelP#1Send Resumes to Jacqueline.Sayoc@KellyScientific.com
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 (https://www.mykelly.com/help-support-working-with-kelly-us/#Benefits) for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.
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