Jobs in South San Francisco, CA

About the role

We are seeking an innovative and highly motivated Process Engineer to join the MSAT team who will contribute significantly to the development of our advanced cell therapy manufacturing platform. This position is responsible for supporting the activities involved in the development, process transfer, compliance, and scalability for Cellares’ manufacturing operations. This individual will focus on technology transfers from Process Development into GMP manufacturing facilities, from South San Francisco to other Cellares sites, as well as drive and develop process automation to improve process reliability, safety, cost-effectiveness, scalability, and compliance. This is a multidisciplinary role requiring the ability to interface with internal and external stakeholders across functional areas to develop the best solutions possible. The successful candidate will be a resident expert in the areas of technology transfer and Manufacturing Science and Technology. It is expected that this individual will work closely with other functional areas and partners to ensure deliverables are met. 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.

What you'll bring

• Bachelor’s Degree in a scientific or related field is required
• A minimum of 3+ years of experience within the biotech/biopharma industry in cGMP Operations
• Experience in the Pharma/Biotech industry in technology transfer
• 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 safety policies of the company and site
• Adherence to cGMPs is required at all times during the manufacturing of Cell Therapy products.
• All personnel are responsible for notifying responsible management in a timely manner of regulatory inspections, serious GMP deficiencies, product defects, and related actions
• Must have experience writing and reviewing GMP documentation
• Strong analytical, problem-solving and critical thinking skills and the ability to lead as a change agent to promote flexibility, creativity, and accountability
• Excellent teamwork and interpersonal skills with the ability to influence and build strong working relationships at all levels within the organization
• Self-awareness, integrity, authenticity, and a growth mindset
• Desire to be part of a rapidly evolving organization with compelling technology and taking products and processes to the next level