Process Engineer III / Senior Process Engineer, MSAT

GeneFab; Alameda (CA); On-site; USD 125,000 - 155,000; Full time

Job summary

An innovative firm is seeking a Process Engineer III to spearhead technology transfer and process optimization in cell and gene therapy manufacturing. This role offers the chance to work in a dynamic environment, managing cross-functional teams and ensuring compliance with cGMP standards. The ideal candidate will leverage their expertise in biopharmaceutical processes to enhance manufacturing efficiency and product quality. Join a forward-thinking company committed to advancing genetic medicines and fostering a diverse workplace where your contributions will make a significant impact.

Qualifications

• 5-7 years of experience in biopharmaceutical process engineering.
• Proven experience in technology transfer and GMP manufacturing.

Responsibilities

• Lead technology transfer projects and develop implementation plans.
• Evaluate manufacturing processes for improvement opportunities.

Skills

Biopharmaceutical Process Engineering

Technology Transfer

Process Development

GMP Manufacturing

Project Management

Cross-Functional Collaboration

Data Analysis

Education

Bachelor's in Engineering

Master's in Biotechnology

Job description

GeneFab is seeking a highly motivated Process Engineer III / Sr. Process Engineer, Manufacturing Sciences and Technology to lead and support internal/external technology transfers and process support activities with high-level technical expertise from development into GMP manufacturing. This role will be responsible for overseeing and facilitating the transfer of new processes and technologies from developmental stages to manufacturing scale, ensuring seamless integration and optimal performance. The ideal candidate should be experienced in cell and gene therapy (autologous and allogeneic) processes and cGMP operations, and comfortable working in a fast-paced, entrepreneurial environment with broad responsibilities and opportunities. The candidate must collaborate effectively with cross-functional teams including Manufacturing Sciences and Technology, Supply Chain, QC, PD, AD, and Quality Assurance, as well as the Client to accomplish deliverables for GMP readiness.

Key Responsibilities: Technology Transfer Management

• Lead technology transfer projects, coordinating with cross-functional teams including Process Development and external partners.
• Develop and implement technology transfer plans, ensuring adherence to timelines and quality standards.
• Conduct risk assessments and development mitigations strategies for technology transfer activities.
• Lead technology transfer discussions between sending units (Process Development and external partners) and receiving units (Manufacturing, QA, QC, SC, AD).
• Responsible for authoring Manufacturing process descriptions, engineering protocols, technical reports, and material specifications. Reviewing and approving manufacturing batch records and any other relevant document to support successful transfer.
• Create feasibility/gap assessments and facility fit analysis for new products and processes.

Key Responsibilities: Process Optimization & Continuous Improvement

• Evaluate manufacturing processes and identify areas for improvement. Propose and implement innovative solutions to enhance process robustness and scalability.
• Implement process enhancements to increase efficiency, reduce costs, and improve product quality.
• Participate in continuous improvement initiatives within MSAT and Manufacturing departments.
• Supervise/conduct lab work to resolve investigations and/or to demonstrate proof-of-concept for proposed changes.

Key Responsibilities: Manufacturing Process Support

• Support process deviation investigations, root cause analyses, and CAPAs.
• Train manufacturing staff on new processes and technologies.

Qualifications:

• Bachelor’s or Masters in a relevant field (e.g., Engineering, Biotechnology, Molecular Biology).
• A minimum of 5-7 years of relevant experience in biopharmaceutical process engineering, with a focus on cell and gene therapy.
• Proven experience in technology transfer, process development, and GMP manufacturing.
• Experience with viral vector manufacturing, cell therapy, and mRNA is a plus.
• Strong communication and project management skills, with a commitment to cross functional collaboration.
• Knowledge of cGMP and regulatory guidelines (e.g., FDA, EMA) and a track record of ensuring compliance.
• Basic understanding of lifecycle management of clinical and commercial manufacturing processes.
• Ability to analyze and interpret data and contextualize with the program goals and requirements in a phase-appropriate manner.

$125,000 - $155,000 a year

Salary is DOE

About GeneFab

GeneFab is a contract manufacturing and synthetic biology biofoundry focused on cell and gene therapies. GeneFab was formed in 2023 with a vision to combine industry leading expertise in synthetic biology with advanced cGMP capabilities in order to accelerate the development and commercialization of genetic medicines. GeneFab offers its customers an extensive technology platform and know-how that spans early stage product design, technical development, and cGMP compliant production. GeneFab's technology platform includes bioinformatic-guided discovery of cell type promoters, directed evolution of small molecule-regulated gene switches, and the engineering of highly sensitive kill switches for enhanced safety and control of cellular therapies.

We are committed to an inclusive and diverse GeneFab. We believe that different perspectives lead to better ideas, and better ideas allow us to better understand the needs and interests of our diverse GeneFab team. We welcome people of different backgrounds, experiences, abilities, and perspectives and are an equal opportunity employer.